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BiC2PAM: constraintguided biclustering for biological data analysis with domain knowledge
Algorithms for Molecular Biology volume 11, Article number: 23 (2016)
Abstract
Background
Biclustering has been largely used in biological data analysis, enabling the discovery of putative functional modules from omic and network data. Despite the recognized importance of incorporating domain knowledge to guide biclustering and guarantee a focus on relevant and nontrivial biclusters, this possibility has not yet been comprehensively addressed. This results from the fact that the majority of existing algorithms are only able to deliver suboptimal solutions with restrictive assumptions on the structure, coherency and quality of biclustering solutions, thus preventing the upfront satisfaction of knowledgedriven constraints. Interestingly, in recent years, a clearer understanding of the synergies between pattern mining and biclustering gave rise to a new class of algorithms, termed as patternbased biclustering algorithms. These algorithms, able to efficiently discover flexible biclustering solutions with optimality guarantees, are thus positioned as good candidates for knowledge incorporation. In this context, this work aims to bridge the current lack of solid views on the use of background knowledge to guide (patternbased) biclustering tasks.
Methods
This work extends (patternbased) biclustering algorithms to guarantee the satisfiability of constraints derived from background knowledge and to effectively explore efficiency gains from their incorporation. In this context, we first show the relevance of constraints with succinct, (anti)monotone and convertible properties for the analysis of expression data and biological networks. We further show how patternbased biclustering algorithms can be adapted to effectively prune of the search space in the presence of such constraints, as well as be guided in the presence of biological annotations. Relying on these contributions, we propose BiClustering with Constraints using PAttern Mining (BiC2PAM), an extension of BicPAM and BicNET biclustering algorithms.
Results
Experimental results on biological data demonstrate the importance of incorporating knowledge within biclustering to foster efficiency and enable the discovery of nontrivial biclusters with heightened biological relevance.
Conclusions
This work provides the first comprehensive view and sound algorithm for biclustering biological data with constraints derived from user expectations, knowledge repositories and/or literature.
Introduction
Biological data are characterized by the presence of local patterns, whose discovery has been widely studied and motivated in the context of biclustering [1, 2]. In particular, the relevance of biclustering has been largely shown in the analysis of gene expression data (to discover transcriptional modules described by subsets of genes correlated in subsets of samples [2]) and biological networks (to unravel meaningfully dense regions from weighted adjacency matrices derived from interaction data [3]). A key question in the field of biclustering is how to benefit from the increasingly available domain knowledge. Initial attempts to incorporate background knowledge from user expectations [4–6] and knowledgebased repositories [7–10] within biclustering showed its importance to explore efficiency gains and guarantee relevant solutions. However, these attempts only support very specific forms of knowledge and cannot be extended to flexibly constrain the desirable properties of outputted biclusters. Furthermore, due to the complexity of the biclustering task^{Footnote 1}, most of the existing algorithms: (1) are based on greedy or stochastic approaches, producing suboptimal solutions; and (2) usually place restrictions on the allowed structure, coherency and quality of biclusters, compromising the flexibility of the outputs [2, 11]. In this context, these biclustering approaches cannot be extended to incorporate knowledgedriven constraints since their restrictions may a priori contradict the inputted constraints.
Recent attempts to perform biclustering based on enhanced pattern mining searches [8, 12, 13], termed as patternbased biclustering, showed the unprecedented possibility to efficiently discover arbitrarily positioned biclusters with parameterizable size, coherency and quality [2, 14]. In this context, two valuable synergies can be identified between patternbased biclustering and knowledge incorporation. First, the optimality and flexibility of patternbased biclustering solutions provide an adequate basis upon which knowledgedriven constraints can be incorporated. Patternbased biclustering tackles the restrictions of peer algorithms, being an adequate candidate to flexibly constrain the desirable properties of the target solution space. Second, the effective use of domain knowledge to guide pattern mining searches has been largely studied in the context of domaindriven pattern mining [15, 16].
Despite these synergies, two major problems persist. First, there is a lack of understanding on whether domaindriven pattern mining and biclustering can be consistently integrated. In particular, there is not a solid ground on how to map the commonly available background knowledge in the form of constraints to guide the biclustering task. Second, patternbased biclustering algorithms depend on a specific variant of pattern mining, referred as fullpattern mining, which has been scarcely studied in the context of domaindriven pattern mining. In fact, although new fullpattern mining searches have been recently proposed to guarantee the scalability of the biclustering task over large and dense data [17, 18], there are not yet contributions on how these searches can be adapted to incorporate background knowledge.
This work addresses these problems. To this end, it extends patternbased biclustering algorithms using principles from domaindriven pattern mining to seize large efficiency gains in the presence of background knowledge. Furthermore, it shows how functional annotations and constraints with succinct, (anti)monotone and convertible properties can be used to guide the biclustering task. The major contributions are fivefold:

integrative view of domaindriven pattern mining and (patternbased) biclustering. The consistency of this view is shown for patterns given by frequent itemsets, association rules and sequences;

principles for biclustering tabular data in the presence of an arbitrary number of annotations per observation (derived from knowledge repositories and literature);

list of meaningful constraints with succinct, (anti)monotone and convertible properties for biological data contexts with a focus on gene expression and network data;

principles to specify, process and incorporate different types of constraints;

extension of fullpattern miners based on patterngrowth searches to optimally explore efficiency gains from constraints with succinct, (anti)monotone and convertible properties. In particular we show:
Figure 1 provides a structured view on the proposed contributions and their applicability.
In this context, we propose BiClustering with Constraints using PAttern Mining (BiC2PAM), an algorithm that integrates recent breakthroughs on patternbased biclustering [3, 14, 19, 20] and extends them to effectively incorporate constraints and annotations from domain knowledge.
Experimental results on synthetic and real data show the importance of incorporating background knowledge within patternbased biclustering to seize large efficiency gains by adequately pruning the search space and to guarantee nontrivial and (biologically) relevant solutions.
This paper is structured as follows. First, we provide background on domaindriven pattern mining for patternbased biclustering. Second, key contributions and limitations from related work are surveyed. Third, we list meaningful constraints in gene expression data and biological networks, and describe an algorithmic basis (BiC2PAM) for their incorporation. BiC2PAM is further extended to attain efficiency gains from constraints with nice properties. Fourth, we provide initial empirical evidence of BiC2PAM’s efficiency and ability to unravel nontrivial yet biologically significant biclusters. Finally, concluding remarks and major implications are synthesized.
Background
Biclustering, fullpattern mining and patternbased biclustering
Definition 1
Given a realvalued matrix A with n rows X = \(\{x_1,\ldots,x_n\}\) and m columns Y = \(\{y_1,\ldots,y_m\}\), and elements \(a_{ij}\) relating row \(x_i\) and column \(y_j\), the biclustering task aims to identify a set of biclusters \(\{B_1,\ldots,B_p\}\), where each bicluster \(B_k\) = \((I_k,J_k)\) is defined by a subset of rows \(I_k\subset X\) and columns \(J_k\subset Y\) satisfying specific criteria of homogeneity and statistical significance.
The homogeneity criteria determine the structure, coherency and quality of biclustering solutions, while the statistical significance of a bicluster determines whether its probability of occurrence deviates from expectations. The homogeneity of a biclustering model is commonly guaranteed through a merit function. Following Madeira’s taxonomy [2], existing biclustering algorithms can be grouped according to their homogeneity criteria (defined by the underlying merit function) and search paradigm (determining how the merit function is applied). The structure of a biclustering solution is essentially defined by the number, size and positioning of biclusters. Flexible structures are characterized by an arbitrary high set of (possibly overlapping) biclusters. The coherency of a bicluster is defined by the observed correlation of values (coherency assumption) and by the allowed deviation from expectations (coherency strength). A bicluster can have coherency of values across its rows, columns or overall elements, where the values typically follow constant, additive, symmetric and orderpreserving assumptions [2]. Finally, the quality of a bicluster is defined by the type and amount of accommodated noise. Definitions 2 and 3 formalize these concepts, while Fig. 2 shows a set of biclusters with different coherencies in a symbolic dataset.
Definition 2
Let the elements in a bicluster \(a_{ij}\in (I,J)\) have coherency across rows given by \(a_{ij}\) = \(k_j+\gamma _i+\eta _{ij}\), where \(k_j\) is the expected value for column j, \(\gamma _i\)is the adjustment for row i, and \(\eta _{ij}\) is the noise factor (affecting the quality of the bicluster). Let \(\bar{A}\) be the amplitude of values in a matrix A. Given a matrix A, the coherency strength is a real value \(\delta \in [0,\bar{A}]\), such that \(a_{ij}=k_j+\gamma _i+\eta _{ij}\) where \(\eta _{ij}\in [\delta /2,\delta /2]\).
Definition 3
The \(\gamma\) factors define the coherency assumption: constant when \(\gamma\) = 0, and additive otherwise. Symmetries can be accommodated on rows, \(a_{ij}\times c_i\) where \(c_i\in \{1,\) −\(1\}\). Orderpreserving assumption is verified when the values of rows induce the same linear ordering across columns.
Definition 4
Given a bicluster B = (I, J), the bicluster pattern \(\varphi _{B}\) is given by the sequence of expected values (\(k_j\)) according to a permutation of columns in the absence of adjustments (\(\gamma _i\) = 0) and noise (\(\eta _{ij}\) = 0): \(\{k_j \mid y_j\in J\}\), while its support is given by the number of rows satisfying the pattern: I.
Consider the additive bicluster (I,J) = (\(\{x_1,x_2\}\),\(\{y_1,y_2,y_3\}\)) in \(\mathbb {N}_0^+\) with coherency across rows. Assuming \(x_{1}J\)= \(\{1,3,2\}\) and \(x_{2}J\) = \(\{3,4,2\}\), then this biclusters can be described by \(a_{ij}\) = \(k_j\) + \(\gamma _i\) with the pattern \(\varphi\) = {\(k_1\) = 0, \(k_2\) = 2, \(k_3\) = 1}, supported by two rows with additive factors \(\gamma _1\) = 1 and \(\gamma _2\) = 3.
Despite the relevance of discovering optimal and flexible biclustering solutions to effectively incorporate knowledgedriven constraints, most of the existing biclustering algorithms are based on greedy or stochastic searches, producing suboptimal solutions, and place restrictions (such as simplistic forms of coherency, fixed number of biclusters, nonoverlapping structures) that prevent the flexibility of the outputs [2, 14].
Patternbased biclustering. In recent years, a clearer understanding of the synergies between pattern mining and biclustering gave rise to a new class of algorithms, referred as patternbased biclustering, aiming to address these limitations (no guarantees of optimality and flexibility). Patternbased biclustering is inherently prepared to efficiently find exhaustive solutions of biclusters with the unprecedented possibility to customize their structure, coherency and quality. Such behavior explains why these algorithms are receiving an increasing attention for biological data analysis [3, 8, 12, 14, 19–21]. The major potentialities include: (1) efficient searches with optimality guarantees; (2) biclusters with flexible coherency strength and assumption [14, 19, 20]; (3) robustness to noise, missing values and discretization problems [14] by introducing the possibility to assign or impute multiple symbols to a single data element; (4) nonfixed number of biclusters arbitrarily positioned [12, 21]; (5) applicability to network data and sparse data matrices [3, 22]; among others.
At its core, patternbased biclustering relies on the (iterative application of the) fullpattern mining task [14]. A fullpattern defines a region from the input data space, thus enclosing not only the underlying pattern (itemset, association rule, sequential pattern or graph with frequency and length above certain thresholds), but also its supporting rows and columns.
Definition 5
Let \(\mathcal {L}\) be a finite set of items, and a pattern P to be a composition of items, either an itemset (\(P\subseteq \mathcal {L}\)), association rule (\(P\,{:}\;P_1\rightarrow P_2\) where \(P_1\subseteq \mathcal {L}\wedge P_2\subseteq \mathcal {L}\)) or sequence ( P = \(P_1\ldots P_n\) where \(P_i\subseteq \mathcal {L}\)). Let a transactional database Dbe a finite set of rows/transactions, each defining a composition of items. A transaction is commonly given by an itemset or sequence. Given D, let the coverage \(\Phi _{P}\) of pattern P be the set of rows in D in which P is satisfied/occurs, and its support \(sup_P\) be the coverage size, \(\Phi _{P}\). Let the length of a pattern P be the number of items.
Definition 6
Given a matrix A, let D be a transactional database derived from A: either the concatenation of items with their column index (transactions given by itemsets) or the ordering of column indexes according to the values per row (transactions given by sequences). A fullpattern is a tuple \((P,\Phi _{P},\psi _P,\Upsilon _P)\), where P is the pattern in D, \(\Phi _{P}\subset X\) is its coverage (rows satisfying P), \(\Psi _P\subset Y\) is the set of indexes (columns), and \(\Upsilon _P\) is the original pattern in A (the corresponding itemset, rule or sequence prior to the concatenation or ordering of column indexes).
Definition 7
Given a matrix A, the mapped transactional database D, and a minimum support \(\theta _1\) and pattern length \(\theta _2\) thresholds, fullpattern mining consists of computing: \(\{(P,\Phi _{P},\psi _P,\Upsilon _P) \mid sup_P \ge \theta _1\wedge P\ge \theta _2\}\).
Figure 3 shows how a symbolic matrix, A, is mapped into two distinct transactional databases (given either by index concatenations or orderings), \(D_1\) and \(D_2\), for the subsequent discovery of fullpatterns. The concatenation of an item \(\sigma \in \mathcal {L}\) with a column index in \(y_i\in Y\) is represented as \(y_i.\sigma\). The fullpattern in \(D_1\) can be formally described as \((\{y_1.6,y_2.5,y_4.3\},\{t_1,t_3\},\{y_1,y_2,y_4\},\) 〈6, 5, 3〉).
Frequent itemsets can be discovered to compose constant, additive and multiplicative models [14]; sequential patterns are used to learn orderpreserving models [19]; and rules can be composed to learn plaid models or tolerate parameterizable levels of localized noise [20]. Figure 3 further illustrates the paradigmatic cases where fullpattern mining is applied to discover constant and orderpreserving biclusters.
In this context, the set of maximal biclusters (bicluster not contained in larger biclusters) are mapped from closed fullpatterns (frequent yet not contained in larger patterns with same support). Definition 8 specifies the mapping between a fullpattern and a bicluster. For realvalued matrices, (realvalued) biclusters are mapped from fullpatterns discovered under a parameterizable coherency strength (\(\delta\) \(\propto\)1/\(\mathcal {L}\) where \(\mathcal {L}\) is the discretization alphabet).
Definition 8
Given a transactional database D derived from a realvalued matrix, the set of maximal biclusters \(\cup _k (I_k,J_k)\) can be derived from the set of closed fullpatterns \(\cup _k P_k\) by mapping \(I_k\) = \(\Phi _{P_k}\) and \(J_k\) = \(\Psi _{P_k}\), where \(\varphi _{B_k}\) = \(\Upsilon _{P_k}\).
Constraintbased biclustering
To formalize the task targeted in this work, we introduce below the concept of constraint in the context of biclustering, and further describe different types of constraints according to the selected fullpattern mining task.
A constraint is traditionally seen as a conjunction of relations (predicate) over a set of variables describing a given dataset [23]. Definitions 9 and 10 revise this notion to guarantee its proper applicability within (patternbased) biclustering tasks.
Definition 9
In the context of pattern mining, a constraint is a predicate on the powerset of items \(C{:}\;2^{\mathcal {L}}\rightarrow\){true,false}. In the context of fullpattern mining, a fullconstraint is a predicate on the powerset of original items, transactions, indexes and/or concatenations, \(C\,{:}\;\{2^{\mathbf {Y}}\times 2^\mathcal {L},2^{\mathbf {X}},2^{\mathbf {Y}},2^{\mathcal {L}}\}\rightarrow\){true,false}. A fullpattern \((P,\Phi _{P},\psi _P,\Upsilon _P)\) satisfies a fullconstraint C if \(C(P,\Phi _P,\psi _P,\Upsilon _P)\) is true.
Definition 10
A biclustering constraint is a predicate on a bicluster’s values per column, rows I, columns J and pattern \(\varphi _B\), \(C\,{:}\;\{2^{\mathbf {Y}}\times 2^\mathcal {L},2^{\mathbf {X}},2^{\mathbf {Y}},2^{\mathcal {L}}\}\rightarrow {true,false}.\) A bicluster B satisfies a constraint C if \(C(\varphi _B\cdot J,I,J,\varphi _B)\) is true (or, alternatively, when the associated fullpattern satisfies a fullconstraint).
Consider a matrix mapped into a transactional database with \(\mathcal {L}\) = {a,b,c}. An illustrative fullconstraint is \(y_1a\in P\wedge \{x_2,x_3\}\) \(\subseteq\) \(\Phi _P\wedge y_4\) \(\in\) \(\Psi _P\wedge \{b\}\) \(\subseteq\) \(\Upsilon _P\), and the associated biclustering constraint is \(y_1a\in B \wedge \{x_2,x_3\}\) \(\subseteq\) \(I\wedge\) \(y_4\in J\wedge \{b\}\) \(\subseteq\) \(\varphi _B\). Minimum support and minimum pattern length are the default fullconstraints in fullpattern mining: \(C_{support}\) = \(\Phi _{P}\ge \theta\) and \(C_{length}\) = \(P\ge \theta\).
More interesting constraints with properties of interest include regular expressions or aggregate functions. In the presence of matrices with numeric or ordinal values, further constraints can be specified. In this context, a cost table is specified in addition to the alphabet of items (e.g. {a:0, b:1, c:2}). Depending on the type of fullpattern, multiple constraints can be applied against a cost table, including the paradigmatic cases of aggregate functions such as length, maximum, minimum, range, sum, mean and variance [24].
Some of these constraints are said to exhibit nice properties when their input can be effectively pushed deep into the pattern mining task [15] to prune the search space and therefore achieve efficiency gains. Below, we explore different types of constraints according to the selected fullpattern mining task for biclustering: itemset, rulebased and sequentialpattern constraints.
Itemset constraints
Regular expressions and aggregate functions are the most common form of constraints to guide frequent itemset mining. In this context, efficiency gains can be seized in the presence of constraints with succinct, (anti)monotone and convertible properties.
Definition 11
Let \(\mathcal {L}\) be a set of items and P be an itemset, \(P\subseteq \mathcal {L}\). Let each item \(\sigma \in \mathcal {L}\) have a correspondence with a real value, \(c{:}\, \mathcal {L}\rightarrow \mathbb {R}\), according to a welldefined cost table. Let v be a realvalued constant and range(P) = max(P) − min(P), max(P) = \(max\bigcup \nolimits _{_\sigma \in P}c(\sigma )\), min(P) = \(min\bigcup \nolimits _{_\sigma \in P}c(\sigma )\) and avg(P) = \(\sum \nolimits _{\sigma \in P}\frac{c(\sigma )}{P}\) be welldefined predicates. In this context:

A constraint C is monotone if for any P satisfying C, P supersets satisfy C (e.g. \(range(P)\ge v\)).

A constraint C is antimonotone if for any P not satisfying C, P supersets do not satisfy C (e.g. \(max(P)\le v\)).

Given a pattern \(P'\) satisfying a constraint C, C is succint over P if P contains \(P'\) (e.g. \(min(P)\le v\)).

A constraint C is convertible with regards to an ordering of items \(R_{\Sigma }\) if for any itemset P satisfying C, the P suffixes satisfy C or/and itemsets with P as suffix satisfy C (e.g. \(avg(P)\ge v\)).
To instantiate the formalized constraints, consider three observations (\(\mathbf {x}_1=\{a,b,c\}\), \(\mathbf {x}_2=\{a,b,c,d\}\), \(\mathbf {x}_3=\{a,d\}\)), a minimum support \(\theta _1\) = 1 and length \(\theta _2\) = 2, and the cost table {a:0, b:1, c:2, d:3}. The set of closed fullpatterns satisfying: the monotone constraint range \((P)\ge 2\) is \(\{(\{a,b,c\},\{t_1,t_2\}),(\{a,d\},\{t_1,t_3\}),\) \((\{b,d\},\{t_2\})\}\); the antimonotone constraint sum \((P)\le 1\) is \(\{(\{a,b\},\{t_1,t_2\})\}\); the succint \(P\supseteq \{c,d\}\) is \(\{(\{a,b,c,d\},\{t_2\})\}\); and the convertible constraint avg \((P)\ge 2\) is \(\{(\{b,c,d\},\{t_2\})\}\).
Association rule constraints
Constraints satisfying these properties can be also effectively applied in the context of association rule mining (for the discovery of noisetolerant biclusters [1, 20]). In this context, constraints need to be satisfied by the antecedent, consequent, or can be alternatively applied during the generation of frequent itemsets, prior to the composition of rules.
Additional constraints to guarantee specific correlation/interestingness criteria [25] or the dissimilarity and minimality of rules [26] can be specified.
In the context of association rulebased biclustering, a fullconstraint is evaluated against the union of items on the antecedent and consequent as well as the union of supporting transactions of the antecedent and consequent. Given \(P{:}\;P_1\rightarrow P_2\) and a constraint C, P satisfies C if the fullpattern given by \((\Upsilon _{P_1\cup P_2},\Phi _{P_1}\cup \Phi _{P_2},\) \(\psi _{P_1\cup P_2},P_1\cup P_2)\) satisfies C.
Sequential pattern constraints
The introduced concepts can be further extended for the incorporation of constraints in the context of sequential pattern mining (for the discovery of orderpreserving biclusters [19]). A sequence P is an ordered set of itemsets, each itemset being a set of indexes in Y. Given a matrix (X, Y) with n = 5 rows and m = 3 columns and a minimum support \(\theta _1\) = 3, (\(y_2\le y_1\wedge y_2\le y_3,\{x_2,x_4,x_5\},\{y_1,y_2,y_3\}\), \(\langle y_2(y_1y_3) \rangle\)) is an illustrative fullpattern. Interestingly, the sequential pattern \(\Upsilon _{P}\) does not explicitly disclose the value expectations \(\varphi _B\). Instead, \(\Upsilon _{P}\) is associated with an ordering relation (such as \(y_2\le y_1\wedge y_2\le y_3\)). In this context, the following constraints can be specified: item constraints (e.g. \(\{y_1,y_3\}\subseteq P\)); length constraints (minimum/maximum number of precedences and/or cooccurrences); superpattern constraints (patterns that contain a particular set of patterns as subpatterns \({}y_2\le y_1\subseteq P\)); and, more interestingly, regular expressions (e.g. \(P\equiv y_{\bullet }\le \{y_{\bullet },y_{\bullet }\}\)). Constraints concerning value expectations can be also specified using the values from a given ordering based on the median of values from the supporting rows and columns (e.g. \(b\le a\) or \(1.3\le 0.4\)). As a result, aggregate functions can be additionally specified within sequential pattern constraints.
With regards to properties of the aforementioned constraints: length constraints are antimonotonic, while superpattern constraints are monotonic. Item constraints, length constraints and superpattern constraints are all succinct. Some aggregate constraints and regular expressions can also show nice properties [27].
Related work
Related work is surveyed according to: (1) the contributions and limitations of existing attempts to perform biclustering with domain knowledge; (2) the stateoftheart on domaindriven pattern mining; and (3) the existing efforts towards fullpattern mining and their adequacy to accommodate domain knowledge.
Knowledgedriven biclustering
The use of domain knowledge to guide biclustering has been increasingly stressed since solutions with good homogeneity and statistical significance may not necessarily be biologically relevant. However, few biclustering algorithms are able to incorporate domain knowledge.
AIISA [7], GenMiner [8] and scatter biclustering [10] are able to annotate data with functional terms retrieved from repositories with ontologies and use these annotations to guide the search.
COBIC [28] is able to adjust its behavior (maximumflow/minimumcut parameters) in the presence of background knowledge. Similarly, the priors and architectures of generative biclustering algorithms [29] can also be parameterized to accommodate specific forms of background knowledge. However, COBIC and its generative peers support only the definition of constraints concerning the algorithm’s behavior and are not able to deliver flexible biclustering solutions.
Fang et al. [4] proposed a constraintbased algorithm enabling the discovery of dense biclusters associated with highorder combinations of singlenucleotide polymorphisms (SNPs). DataPeeler [5], as well as algorithms from formal concept analysis [6] and bisets mining [30], are able to efficiently discover dense biclusters in binary matrices in the presence of (anti)monotone constraints. However, these algorithms impose a very restrictive form of homogeneity in the delivered biclusters.
Domaindriven pattern mining
A large number of studies explored how constraints can be used to guide pattern mining tasks. Two major paradigms are available: constraintprogramming (CP) [16] and dedicated searches [15, 31]. CP allows pattern mining to be declaratively defined according to sets of constraints [16, 32]. These declarative models can allow for complex mathematical expressions on the set of fullpatterns. Nevertheless, due to the poor scalability of CP methods, they have been only used in highly constrained settings, smalltomedium sized data, or to mine approximate patterns [16, 32].
Pattern mining searches have been adapted to seize efficiency gains from different types of constraints [15, 31, 33]. These efforts aim to replace naïve solutions based on postfiltering to guarantee the satisfaction of constraints. Instead, the constraints are pushed as deep as possible within the mining step for an optimal pruning of the search space. The nice properties exhibited by constraints, such as antimonotone and succinct properties, have been initially seized in the context of frequent itemset mining by Apriori methods [31] to affect the generation of candidates. Convertible constraints can hardly be pushed in Apriori methods but can be adequately handled by pattern growth methods such as FPGrowth [15]. FICA, FICM, and more recently MCFPTree [15], are FPGrowth extensions to further explore opportunities from diverse constraints. The inclusion of monotone constraints is more complex. Filtering methods, such as ExAnte [34], are able to combine antimonotone and monotone pruning based on reduction procedures. Empirical evidence shows that these reductions are optimally handled within pattern growth methods by adequately growing and pruning small FPTrees (referred as FPBonsais) [33].
These contributions were extended for association rule mining [33, 35]. In particular, nice properties were studied for item constraints [35], support constraints [36], bounds interestingness criteria [37], and constraints on the structure and dissimilarity of rules (respectively referred as schema and opportunistic) [38].
Similarly, some studies proposed ways to effectively incorporate constraints within Apriori and patterngrowth searches for sequential pattern mining (SPM) [27, 39]. Apriori searches were first extended to incorporate temporal constraints and userdefined taxonomies [39]. Mining frequent episodes in a sequence of events [40] can also be viewed as a constrained SPM task by seeing episodes as constraints in the form of acyclic graphs. SPIRIT [41] revises the Apriori search to incorporate a broader range of constraints with nice properties and regular expressions. Pattern growth searches based on data projections, such as PrefixSpan, were only later extended by Pei et al. [27, 42] to support a wideset of constraints with nice properties. Although multiple studies have been proposed on the use of temporal constraints for SPM, including length and gap constraints [27, 43], these constraints are not relevant for the aim of learning orderpreserving models.
Fullpattern mining with constraints
There are three major classes of fullpattern mining searches [1, 44, 45]: (1) AprioriTIDbased searches, generally suffering from costs of candidate generation for dense datasets and low support thresholds; (2) searches with vertical projections, which show efficiency bottlenecks for data with a high number of transactions since the bitset cardinality becomes large and associated intersection procedures expensive; and (3) recently proposed patterngrowth searches based on the annotation of original patterngrowth structures with transactions’ identifiers. In particular, F2G [17] and IndexSpan [18] (default options in BicPAM, BiP, BicNET and BicSPAM biclustering algorithms [14, 19, 20, 22]) were the first patterngrowth searches for fullpattern mining aiming to surpass memory and time bottlenecks associated with bitset and diffset structures used by AprioriTID and verticalbased searches.
Despite the high number of contributions from domaindriven pattern mining, the ability of patterngrowth searches to effectively incorporate fullconstraints with nice properties (Definition 9) was not yet demonstrated.
Solution: Patternbased biclustering with domain knowledge
This section extends patternbased biclustering algorithms [1] to accommodate constraints by proposing BiC2PAM (BiClustering with Constraints using PAttern Mining). In what follows, we first provide principles for biclustering annotated biological data. Second, meaningful fullconstraints with nice properties are listed to guide expression data analysis and network data analysis. The possibility to specify alternative constraints in order to customize the structure, coherency, quality and statistical significance of biclustering solutions according to available knowledge is discussed in Appendix. Third, we describe a set of principles for the specification, processing and incorporation of constraints within patternbased biclustering. Finally, we adapt the fullpattern mining searches used within BiC2PAM in order to seize heightened efficiency gains by exploring the properties associated with the inputted constraints.
Biclustering with annotations extracted from knowledge repositories and literature
Domain knowledge comes often in the form of annotations associated with specific rows and columns in a matrix (or nodes in a network). These annotations are often retrieved from knowledge repositories, semantic sources and/or literature. Annotations can be either directly derived from the properties associated with each row/column/node (e.g. properties of a gene or a sample in gene expression data) or can be implicitly predicted based on the observed values by using feature extraction procedures. For instance, consider the set of functional annotations associated with gene ontology (GO) terms [46]. A GO term is associated with an interrelated group of genes associated with a specific biological process. Since a gene can participate in multiple biological processes, genes can have an arbitrary number of functional annotations. As such, rows in an expression matrix (or nodes in a biological network) can be annotated with a nonfixed number of labels.
Patternbased biclustering supports the integrated analysis of matrices and annotations recurring to one of two strategies. First, association rules or sequential rules can be used to guide the biclustering task in the presence of annotations according to the principles introduced by Martinez et al. [8]. In this context, annotations can either appear in the consequent, antecedent or on both sides of an association rule. Biclusters can then be inferred from these rules using the principles introduced by Henriques et al. [1]. Illustrating, a rule \(\{y_12,y_42\}\rightarrow \{T_1, T_2\}\) supported by \(\{x_1,x_3,x_5\}\) rows can be used to compose a bicluster \((\{y_1,y_4\},\{x_1,x_3,x_5\})\) with elements consistently associated with annotations \(T_1\) and \(T_2\). Learning association rules with levels of confidence (or alternative interestingness scores) below 100 % [20] is relevant to discover biclusters with consistent annotations without imposing a subset of annotations to appear on all rows/columns of each bicluster.
Second, the annotations can be included directly within data since pattern mining is able to rely on rows with an arbitrary length. To this aim, annotations are associated with a new dedicated symbol and appended to the respective rows, possibly leading to a set of observations with varying length. Consider the annotations \(T_1\) and \(T_2\) to be respectively associated with genes \(\{x_1,x_3,x_4\}\) and \(\{x_3,x_5\}\), an illustrative transactional database of itemsets for this scenario would be \(\{x_1=\{a_{11},\ldots,a_{1m},T_1\},x_2=\{a_{21},\ldots,a_{2m}\},x_3=\{a_{31},\ldots,a_{3m},T_1,T_2\},\ldots\}\). Databases of sequences (for orderpreserving biclustering) can be composed by appending terms either at the end or the beginning of each sequence.
Given these enriched databases, pattern mining can then be applied on top of these annotated transactions with succinct, (anti)monotone and convertible constraints. Succinct constraints can be incorporated to guarantee the inclusion of certain terms (such as \(P\cap \{T_1,T_2\}\) \(\ne\) 0). This is useful to discover, for instance, biclusters with genes participating in specific functions of interest. (Anti)monotone convertible constraints can be, alternatively incorporated to guarantee, for instance, that a bicluster associated with a discovered pattern is functionally consistent, meaning that it can be mapped to a single annotation. The \(P\cap \{T_1,T_2\}\ge 1\) constraint is antimonotone and satisfies the convertible condition: if P satisfies C, the P suffixes also satisfy C.
Interestingly, the two previous strategies can be seen as equivalent when assuming that the discovery of the introduced class of association rules is guided by rulebased constraints and the discovery of patterns from annotated data is guided by itemset/sequence constraints.
Biological constraints with properties of interest
Different types of constraints were introduced in Definition 11. In order to show how these constraints can be specified and instantiated, this section provides examples of meaningful constraints for gene expression and network data analysis.
Note that similar constraints can be formulated for the analysis of alternative biological data, including: structural genome variations to enable the discovery of highorder singlenucleotide polymorphisms; genomewide data to find promoters where mutations or appearing binding sites show properties of interest; or medical data to force the inclusion of certain clinical features or to focus on lesstrivial disease markers.
Gene expression data analysis
For illustrative purposes, consider Fig. 4 to be associated with a symbolic expression matrix (and associated “price table”), where the rows in the matrix correspond to different genes and their values correspond to the observed expression levels for a specific condition (column). The {−3,−2}, {−1,0,1} and {2,3} sets of symbols are respectively associated with repressed (downregulated), default (preserved) and activated (upregulated) expression levels.
First, succinct constraints in gene expression analysis allow the discovery of genes with specific constrained levels of expression across a subset of conditions. Illustrating, \(min(\varphi _B)\) = −3 implies an interest in biclusters (putative biological processes) where genes are at least highly repressed in one condition. Alternatively, succinct constraints can be used to discover nontrivial biclusters by focusing on nonhighly differential expression (e.g. patterns with symbols {−2,2}). Such option contrasts with the large focus on dense biclusters [2], thus enabling the discovery of lesstrivial yet coherent modules.
Second, (anti)monotone constraints are key to capture background knowledge and guide biclustering. For instance, the nonsuccinct monotonic constraint countVal \((\varphi _B)\ge 2\) implies that at least two different levels of expression must be present within a bicluster (putative biological process). In gene expression analysis, biclusters should be able to accommodate genes with different ranges of upregulation and/or downregulation. Yet, the majority of existing biclustering approaches can only model a single value across conditions [2, 14]. When constraints, such as the valuecounting inequality, are available, efficiency bottlenecks can be tackled by adequately pruning the search space.
Finally, convertible constraints also play an important role in biological settings to guarantee, for instance, that the observed patterns have an average of values within a specific range. Illustrating, the antimonotonic convertible constraint \(avg(\varphi _B)\le 0\) indicates a preference for patterns with repression mechanisms without a strict exclusion of activation mechanisms. These constraints are useful to focus the discovery on specific expression levels, while still allowing for noise deviations. Understandably, they are a robust alternative to the use of strict bounds from succinct constraints with maximum–minimum inequalities.
Biological network data analysis
To motivate the relevance of inputting similar constraints for the analysis of biological networks, we use again the tabular dataset provided in Fig. 4. In this context, rows and columns correspond to nodes associated with biological entities (such as genes, proteins, protein complexes or other molecular compounds), and the values in the matrix correspond to the strength of the interactions between the nodes. As such, the strength of the interactions is either negative {−3, −2} (e.g. inhibition), weak {−1, 0, 1} or positive {2, 3} (e.g. activation).
First, succinct constraints can be specified for the discovery of sets of nodes with specific interaction patterns of interest. Illustrating, \(\{2,2\}\subseteq \varphi _B\) implies an interest on nondense network modules (coherent interactions with soft inhibition and activation) to disclose nontrivial regulatory activity, and \(min(\varphi _B)=3\wedge max(\varphi _B)=3\) implies a focus on modules with the simultaneous presence of highly positive and negative interactions.
Second, (anti)monotone constraints are key to discover network modules with distinct yet coherent regulatory interactions. For instance, the nonsuccinct monotonic constraint countVal \((\varphi _B)\ge 3\) implies that at least three different types of interactions must be present within a module.
Finally, convertible constraints are useful to place nonstrict expectations on the desirable patterns, yet still accommodating deviations from expectations. Illustrating, \(avg(\varphi _B)\le 0\) indicates a preference for network modules with negative interactions without a strict exclusion of positive interactions.
Constraints with nice properties can be alternatively applied for networks with qualitative interactions. Regulatory interactions, such as “binds”, “activates” or “enhances”, are increasingly observed for a widevariety of proteinprotein and gene interaction networks [47, 48]. In this context, assuming the presence of {a, b, c} types of biological interactions, an illustrative antimonotone constraint is \(\varphi _B\cap \{a,b\}\ge 0\).
Biological data analysis with fullconstraints
Although less motivated, constraints can be also defined on the powerset of rows, columns and/or values per columns. In fact, the minimum support and minimum pattern length can be seen as constraints over I and J indexes, respectively. An alternative constraint over I and J is to require that biclusters include a minimum number rows/columns from a particular subset of rows/columns of interest. An illustrative succinct constraint in \(Y\times \mathcal {L}\) is \(P\cap \{y_2\)\(3,y_23\}\ne \emptyset\), which implies an interest in biclusters with differential expression (or interactions) associated with the \(\mathbf {y}_2\) sample/gene/node.
Please have in mind that the constraints instantiated throughout this section represent a small subset of all possible constraints of interest, thus being mainly introduced for the sake of motivating the relevance of succinct, (anti)monotone and convertible properties. The specification of constraints of interest is always dependent on the learning goal and the peculiarities of the input data. As such, an exhaustive listing and discussion of relevant constraints for biological data contexts is considered to be out the scope of this work.
Biclustering with fullconstraints
We propose BiClustering with Constraints using PAttern Mining (BiC2PAM) to effectively incorporate fullconstraints (including the set of constraints motivated in previous section). BiC2PAM’s extensions to the existing contributions on patternbased biclustering [12, 14, 19, 20, 22] are twofold. First, a precise formalism was defined to represent fullconstraints (with identical notation to the one introduced along this work) and new processing procedures were implemented for their parsing and interpretation. Under these principles, the desirable properties of biclustering solutions can be defined with sharp usability. BiC2PAM supports not only the specification of fullconstraints (Definition 10), but further makes available the possibility to specify native constraints to customize the structure, coherency and quality of biclustering solutions (as described in Appendix). Second, BiC2PAM implements different strategies to incorporate distinct types of constraints:

if native constraints are inputted, BiC2PAM maps them into parameterizations along the mapping, mining and closing steps of BicPAMS (Appendix);

if constraints without nice properties are inputted, BiC2PAM satisfies them recurring to postfiltering verifications;

if constraints with nice properties are inputted, BiC2PAM implements pruning heuristics from previous research on constraintbased Aprioribased methods [36, 41].
In the context of the formal view on constraintbased fullpattern mining introduced in "Constraintbased biclustering" section, when constraints over \(\Upsilon _P\) (constraints in \(2^{\mathcal {L}}\)) are inputted, they are mapped as constraints over \(P\in 2^{Y\times \mathcal {L}}\). For instance, the \(a\in \Upsilon _P\) succinct constraint is mapped as \(P\cap \{y_1a,\ldots y_ma\}\ne \emptyset\).
Similarly, constraints from \(\psi _P\in 2^{Y}\) are mapped to constraints over \(P\in 2^{Y\times \mathcal {L}}\). Illustrating, \(y_2\in Y\) is mapped as \(P\cap \{y_2a,y_2b,\ldots\}\ne \emptyset\).
Finally, constraints from \(\Phi _P\in 2^{X}\) are incorporated by adjusting the Apriori searches to effectively prune the search space. Consider a succinct constraint that specifies a set of transactions to be included in the resulting biclusters. In this case, as soon as a generated candidate is no longer supported by any transaction of interest, there is no need to further generate new candidates and, thus, the search space can be pruned at this point.
Understandably, despite the inherent simplicity of incorporating constraints with nice properties in Aprioribased searches, there is a critical drawback: the inability to rely on key patterngrowth searches, such as F2G (for the discovery of constant/additive/symmetric/plaid biclusters) and IndexSpan (for the discovery of orderpreserving biclusters). These patterngrowth searches were previously shown to be able to mine large data with superior efficiency [17, 18]. Adding to this observation, there is a considerable agreement that the underlying structures of patterngrowth searches, such as frequentpattern trees and prefixgrowth trees, provide a more adequate representation of the search space for an improved pruning.
Exploring efficiency gains from constraints with nice properties
Although the incorporation of constraints with nice properties can only be easily supported under Aprioribased searches, there is large consensus that patterngrowth searches are better positioned to seize efficiency gains from these constraints than peer Aprioribased and vertical searches. As such, F2GBonsai and IndexSpanPG, described below, extend respectively the recently proposed F2G (fullfrequent itemset miner) and IndexSpan (fullsequential pattern miner) algorithms to guarantee a more effective pruning of the search space in the presence of constraints. These extensions are integrated in BiC2PAM. Native constraints are effectively incorporated in BiC2PAM through adequate parameterizations of patternbased biclustering algorithms (Appendix).
F2GBonsai: F2G with itemset constraints
F2G [17] implements a patterngrowth search that does not suffer from efficiency bottlenecks of peer searches since it relies on frequent pattern tree structures (FPtrees) that store transactionIDs without duplicates. The FPtree is efficiently traversed to enumerate all fullpatterns. Fullpatterns are generated by concatenating the pattern suffixes with the fullpatterns discovered from conditional FPtrees where suffixes are removed. Figure 5 instantiates the behavior of F2G. In this section, we first show the compliance of F2G with principles to handle succinct and convertible constraints [15]. Second, we show its compliance to handle difficult combinations of monotone and antimonotone constraints [33].
Compliance with different types of constraints
Unlike candidate generation methods, pattern growth searches provide further pruning opportunities. Pruning principles can be standardly applied on both the original database (FPTree) and on each projected database (conditional FPTree).
The CFG method extends patterngrowth searches [15] to seize the properties of nice constraints using simplistic principles. Supersets of itemsets violating antimonotone constraints are removed from each (conditional) FPTree. Illustrating, in the presence of \(sum(\Upsilon _P)\le 3\), when analyzing the \(y_12\) conditional database, the following items \(\cup _{i=1}^{m} \{y_i2,y_i3\}\) can be removed to avoid conflicts as their sum violates the given constraint. For an effective pruning, it is recommended to order the symbols in the header table according to their value and support [15, 24]. F2G is compliant with these pruning heuristics, since it allows the rising of transactionIDs in the FPTree according to the order of candidate items for removal in the header table (see Algorithms 1 and 2 in [17]).
For the particular case of an antimonotone convertible constraint, itemsets that satisfy the constraint are efficiently generated under a patterngrowth search [24]. This is done by assuming that original/conditional FPtrees are built according to a price table and by pruning patterns that no longer satisfy an antimonotone convertible constraint since the inclusion of new items will no longer satisfy the constraint. Illustrating, since \(\{y_1\)−\(3,y_42,y_23\}\) does not satisfies \(avg(\Upsilon _P)\le 0\), there is no need to further build \(\{y_1\)−\(3,y_42,y_23\}\)conditional trees. Therefore, this principle provides an important criterion to stop FPtree projections and/or prune items in a (conditional) FPtree.
Finally, the transactions and items within a (conditional) FPtree that conflict with a given constraint can be directly removed without causing any changes on the resulting set of valid patterns. Illustrating, given \(min(\Upsilon _P)=0\) constraint, the transactions \(\mathbf {x}_1=\{y_1\)−\(1,y_23,y_31\}\) and \(\mathbf {x}_4=\{y_11,y_2\)−\(1,y_32\}\) can be directly removed as they do not satisfy this succinct constraint. Similarly, given the same constraint, \(min(\Upsilon _P)=0\), the items with values below 0 can be removed. With regards to transactions \(\mathbf {x}_1\) and \(\mathbf {x}_4\), this means removing \(a_{1,1}=y_1\)−1 and \(a_{4,2}=y_2\)−1 items.
Furthermore, constraint checks can be avoided for subsets of itemsets satisfying a monotone constraint. Illustrating, no further checks are needed in the presence of countVal \((\Upsilon _P)\ge 2\) constraint when the range of values in the suffix of a pattern is \(\ge\)2 under the \(\{y_10,y_11\}\)conditional FPTree.
Combination of constraints with nice properties
The previous extensions to patterngrowth searches are not able to effectively comply with monotone constraints when antimonotone constraints (such as minimum support) are also considered. In FPBonsai [33], principles to further explore the monotone properties for pruning the search space are considered without reducing antimonotone pruning opportunities. This method is based on datareduction operations originally implemented in ExAnte to seize efficiency gains from the properties of monotone constraints. There are two datareductions: \(\mu\)reduction, which deletes transactions not satisfying C; and \(\alpha\)reduction, which deletes from transactions single items not satisfying C. Thanks to the recursive projections of FPgrowth, the ExAnte datareduction methods can be applied on each conditional FPtree to obtain a compact number of smaller FPTrees (FPBonsais). The FPBonsai method can be combined with the previously introduced principles, which are particularly prone to handle succinct and convertible antimonotone constraints. F2G can be extended to support these reductions on the (conditional) FPTrees by guaranteeing that transactions consistently rise up. The only requirement is to preserve the order of items in the header table [17]. As such, F2G complies with the FPBonsai extension (see Algorithm 2).
IndexSpanPG: IndexSpan with sequential pattern constraints
The work of Pei et al. [27] provides principles to extend patterngrowth searches with prefixbased database projections and no candidate generation to effectively incorporate regular expressions and constraints with nice properties. For this aim, the prefixmonotone property is defined. A constraint is called prefixmonotone if it is prefix antimonotonic or prefix monotonic. With a prefixmonotone constraint, there is only the need to search in the projected databases for prefixes that satisfy the constraint. When a constraint C is: (1) prefix antimonotonic, if C(P) = false, then there exists no sequential patterns containing P has a prefix and also satisfies C; (2) prefix monotonic, if C(P) = true, then every sequential pattern having P as a prefix satisfies C; and (3) a regular expression, if the prefix of a given sequential pattern is conflicting with the regular expression C, then there is no need to further expand (i.e. there are no sequential patterns with the same prefix that also satisfy C). As such, since monotonic, antimonotonic and regular expression constraints are prefixmonotone they can be pushed deep into the search. Understandably, the efficiency gains associated with such constraints cannot be attained under Aprioribased searches [41]. Although succinct constraints are not necessarily prefix antimonotonic or prefix monotonic, they can also be easily pushed deep into the mining process (independently of the applied SPM method).
According to these principles, we extended IndexSpan [18], an extension of PrefixSpan to explore efficiency gains from the intrinsic properties of the orderpreserving biclustering task. IndexSpan is compliant with the enumerated principles. The minimalist data structures, fast database projections and early pruning techniques [18] do not interfere with the underlying prefixgrowth behavior, the essential requirement to incorporate prefixmonotone constraints. Furthermore, given the fact that IndexSpan explores itemindexable properties associated with the orderpreserving biclustering task, testing constraints is done in an efficient and elegant way (see Algorithm 3). This is true with regards to both: (1) the validation of whether an antimonotonic constraint (or regular expression) cannot be satisfied by a given prefix (in order to stop its growth), and (2) the validation of whether a a monotonic constraint cannot be satisfied by a given (projected) sequence (in order to prune the search).
BiC2PAM: algorithmic details
The algorithmic basis of BiC2PAM is described in Algorithm 1. The behavior of BiC2PAM can be divided according to four major steps: (1) preprocessing, (2) instantiation of constraints, (3) mining and (4) postprocessing. In step 1, the input realvalued matrix is discretized (after proper normalization and exclusion of outliers) under a given coherency strength, and multiple items assign to values near a boundary of discretization (according to [14]). If, instead, a network is given as input, it is mapped into a sparse adjacency matrix (according to [3]). Still along this first step, transactional and sequential databases are mapped from the previous data structures. In step 2, the inputted constraints are parsed, their soundness checked against the preprocessed databases, and used to parameterize BiC2PAM (if native) or instantiated (otherwise). In step 3, the pattern mining searches proposed in "Exploring efficiency gains from constraints with nice properties" section are applied over the mapped databases and inputted constraints with a decreasing support until a prespecified number of patternbased biclusters (or coverage of matrix elements) satisfying these constraints is achieved. Finally, BiC2PAM allows for the postprocessing of the discovered biclusters to guarantee their robustness and dissimilarity by recurring to merging, extension, reduction and filtering procedures (step 4 according to [14]). Figure 6 provides a simplified illustration of these major steps.
Understandably, the behavior and performance of Algorithm 1 is essentially dependent on the underlying domaindriven pattern mining searches. Algorithms 2 and 3 respectively describe F2GBonsai and IndexSpanPG in accordance with the pruning principles respectively introduced in "F2GBonsai: F2G with itemset constraints" and "IndexSpanPG: indexSpan with sequential pattern constraints" sections. In F2GBonsai, reductions of the search space are efficiently applied during the creation of the initial FPtree and of each conditional FPtree (lines 7 and 32). Succinct, monotone, frequency and antimonotone reductions are efficiently applied in this order. In IndexSpanPG, the pruning of conflicting sequences or items with sequential constraints is done after the initial construction of the itemindexable database and after each database projection (lines 6, 24 and 29). Moreover, the growing of a given prefix is stopped whenever the prefix contradicts an antimonotonic constraint or regular expression (lines 21 and 26). In order to avoid an unnecessary overhead for biclustering tasks in the presence of high number of constraints, the pruning principles in F2GBonsai and IndexSpanPG might be only applied for certain database projections. In this case, the periodicity \(\tau\) of projections eligible for pruning should be given as input to the algorithms (\(\tau\) = 1 by default).
The computational complexity of BiC2PAM is bounded by the complexity of the patternbased biclustering task in the absence of constraints. The complexity of patternbased biclustering tasks for dense and sparse matrices can be respectively consulted in the documentation of BicPAM [14] and BicNET [3].
BiC2PAM also provides default behaviors in order to guarantee a friendly environment for users without expertise in biclustering. For this aim, BiC2PAM makes available: (1) default parameterizations (dataindependent setting) and (2) dynamic parameterizations (datadependent setting). Default parameterizations include: (1) zeromean roworiented normalization followed by overall Gaussian discretization with n/4 items for orderpreserving coherencies (for an adequate tradeoff of precedences vs. cooccurrences) and a set of \(\{3,5,7\}\) items for the remaining coherencies; (2) iterative discovery of biclusters with distinct coherencies (constant, symmetric, additive and orderpreserving); (3) F2GBonsai search for closed FIM and association rule mining, and IndexSpanPG search for SPM; (4) multiitem assignments; (5) merging of biclusters with over 70 % Jaccardbased similarity; (6) a filtering procedure for biclusters without statistical significance (according to [49]) and a 60 % Jaccardbased similarity against a larger bicluster; and (7) no constraints. For the default setting, BiC2PAM iteratively decreases the support threshold by 10 % (starting with \(\theta\) = 80 %) until the output solution discovers 50 dissimilar biclusters or a minimum coverage of 10 % of the inputted matrix elements or network interactions. Dynamic parameterizations enable the: (1) selection of datadriven normalization and discretization procedures according to their fitting error, and (2) activation of data partitioning procedures for large matrices: over 100 million elements (excluding missing values) for the discovery of constant biclusters and over 1 million elements for the remaining coherencies.
Results
This section provides empirical evidence of the soundness of the proposed contributions and of the relevance of using constraints within (patternbased) biclustering to prune the search space and guarantee biologically significant solutions. To this end, we assessed the performance of BiC2PAM on synthetic data, gene expression data and biological networks in the presence of domain knowledge. BiC2PAM was parameterized with default behavior and applied with F2GBonsai for the discovery of constant biclusters with itemset constraints and with IndexSpanPG for the discovery of orderpreserving biclusters with sequential pattern constraints. The stopping criteria of BiC2PAM was specified as a minimum of 20 dissimilar biclusters for synthetic data contexts and 50 dissimilar biclusters for real data contexts. BiC2PAM is implemented in Java (JVM v1.6.024). The experiments were computed using an Intel Core i5 2.30GHz with 6GB of RAM.
Results on synthetic data
Synthetic data
Table 1 describes the generated data settings, with properties resembling the regularities of gene expression data. Constant and orderpreserving biclusters with varying quality and coherency strength were generated. Noise factors (±20 % of the range of inputted values) were imputed and overlaps between biclusters allowed. The selected number of rows and columns per bicluster follows a Uniform distribution using the ranges in Table 1 in order to guarantee the inclusion of biclusters with dissimilar shapes. Reported results are the average of performance views collected from 30 data instances per setting.
Uninformative elements
A simplistic yet relevant form of domain knowledge is the knowledge regarding the uninformative elements of a given dataset. To this end, the ranges of values (or symbols) to remove can be specified under a succinct constraint \(S\notin P\) where \(S\subseteq \mathbb {R}^+\) (or \(S\subseteq \mathcal {L}\)). The application of this constraint within BiC2PAM leads to the removal of these elements prior to the mining step, resulting in significantly large efficiency gains as shown by Fig. 7. This figure describes the impact of removing a varying extent of uninformative elements from synthetic data on the biclustering task. Despite the simplicity of this constraint, existing biclustering algorithms are not able to support this behavior, which undesirably impacts their efficiency and the adequacy of the outputted biclustering solutions.
Incorporating annotations
Figure 8 assesses the ability of BiC2PAM to discover biclusters with functional consistency from annotated data. Functional consistency is observed when the majority of rows in a bicluster share one or more annotations. To this end, we annotate 2000 × 200 matrices with a varying number of annotations per row^{Footnote 2}, {10 ± 4, 4 ± 2}, where each annotation is observed on a varying number of rows, {200 ± 10, 100 ± 10}. For this analysis, we guaranteed that the hidden biclusters have a high degree of functional consistency by imposing that the majority (85 % ± 10 pp) of their rows share a common annotation. As such, BiC2PAM was parameterized with succinct constraints guaranteeing that at least one annotation is consistently observed for all the rows of each bicluster before postprocessing (before the application of extension, merging and reduction procedures). Despite the higher complexity from mining heterogeneous data (input data plus a large amount of annotations), results show that BiC2PAM is in fact more efficient than the baseline option. Furthermore, the observed match scores suggests that the presence of annotations may play an important role in guiding the recovery of true biclusters.
Itemset constraints
In order to test the ability of BiC2PAM to seize efficiency gains in the presence of itemset constraints with nice properties, we applied BiC2PAM over the 2000 × 200 data setting (generated with 5 background symbols \(\mathcal {L}\) = {−2, −1, 0, 1, 2} and hidden biclusters with constant assumption) in the presence of succinct, monotone and convertible constraints. For the baseline performance, constraints were satisfied using postfiltering procedures. Figure 9 shows the impact of inputting disjunctions of succinct constraints in the performance of BiC2PAM. As observed, the ability of BiC2PAM to effectively prune the search space in the presence of these constraints is associated with significant efficiency gains. Moreover, they enable a focus on lesstrivial regions from the input data space (e.g. −1 \(\in\) \(\varphi _B\vee 1\) \(\in\) \(\varphi _B\)).
Figure 10 measures the performance of BiC2PAM when constraints with monotone, antimonotone and convertible properties are inputted. To this end, we show the efficiency gains from parameterizing the underlying F2G miner with diverse principles, and further test F2G’s ability to deal not only with constraints satisfying a single property but multiple properties of interests (e.g. \(\gamma _1<sum(\varphi _B)<\gamma _2\)). Results confirm that the proposed enhancements can lead to a substantial pruning of the search space. In particular, CFG principles [15] are used to seize efficiency gains from convertible constraints and FPBonsai [33] to seize efficiency gains from monotonic constraints.
Sequential pattern constraints
Figure 11 extends the previous analyses towards the constraintguided discovery of orderpreserving biclusters with regular expressions. For this analysis, BiC2PAM was parameterized with IndexSpan and IndexSpanPG and applied over the 1000 × 100 setting with a varying set of constraints (minimum number of precedences and ordering constraints). Results show that increased efficiency gains can be attained from pruning data regions that do not satisfy these constraints.
Fullpattern growth searches
The previous results highlight the relevance of fullpattern growth searches for biclustering (F2GBonsai and IndexSpanPG) to adequately prune the search space. Figure 12 further motivates the importance of the proposed F2GBonsai against AprioriTID and Eclat (F2G is able to surpass efficiency bottlenecks associated with bitset data structures), and the relevance of IndexSpanPG against PrefixSpan (IndexSpan is able to explore further efficiency gains from the itemindexable properties of the biclustering task). Results show the relevance of parameterizing BiC2PAM with the proposed fullpattern growth searches for large data and for hidden biclusters with loose coherency strength (highly dense data).
Results on biological data
Real data
To assess BiC2PAM over real data, we selected expression and network datasets with varying properties. Four gene expression datasets were considered: dlblc (660 genes, 180 conditions) with human responses to chemotherapy [50], hughes (6300 genes, 300 conditions) to study nucleosome occupancy [51], and yeastcycle (6221 genes, 80 conditions) and gasch (6152 genes, 176 conditions) measuring yeast responses to environmental stimuli [52]. Three biological networks from STRING v10 database [53] were additionally considered. These networks capture the gene interactions within human (6314 nodes, 423,335 interactions), Escherichia coli (8428 nodes, 3,293,416 interactions) and yeast (19,247 nodes, 8,548,002 interactions) organisms. The scores in these networks are inferred from literature and multiple data sources, revealing the expected strength of correlation between genes.
Uninformative elements
In gene expression data analysis, elements from the input matrix with default/nondifferential expression are generally less relevant. Similarly, in the context of network data analysis, interactions with low weights are generally of reduced interest for module discovery. In these contexts, these data elements can be removed from the learning under a succinct constraint. Figures 13 and 14 measures the impact of inputting such succinct constraints on the efficiency of BiC2PAM and on the properties of the outputted biclusters (assuming constant coherency). For this analysis, we analyze performance of BiC2PAM on both expression data (Fig. 13) and network data (Fig. 14) from different organisms. Results show that by inputting such simplistic constraints, very high efficiency gains can be obtained. Additionally, the removal of uninformative elements allows the focus on more relevant regions of the input data space and is associated with slightly smaller biclusters due to the greater ability to exclude such elements from the solution space.
Annotations
Figure 15 measures the impact of incorporating functional terms from ontologies for the analysis of biological data (assuming an underlying constant coherency). To this end, we collected for each gene from human and yeast organisms the set of functional terms associated with the biological processes represented in gene ontology from GOToolBox [46]. BiC2PAM was then applied over expression and network data in the presence of these annotations. Results confirm that BiC2PAM is able to integratively learn from data and annotations without further costs in efficiency, and to guarantee the functional consistency of the outputted biclusters (as expectedly demonstrated by the analysis of the enriched terms).
Succinct, monotone and convertible constraints
Figures 16 and 17 show the impact of inputting biologically meaningful constraints in the efficiency and effectiveness of BiC2PAM. For this purpose, we used the complete gasch dataset (6152 × 176) [54] with five levels of expression (\(\mathcal {L}\) = 6). The impact of considering a diverse set of constraints in the efficiency levels of BiC2PAM is provided in Fig. 16. The observed results demonstrate the relevance of using meaningful constraints with succinct, (anti)monotone and convertible properties not only to guarantee a userguided focus on specific regions of interest, but also to promote the tractability to perform biclustering to solve computationally complex biological problems and analyzes.
The impact of these constraints in the relevance of patternbased biclustering solutions is presented in Fig. 17. The biological relevance of each bicluster was derived from the analysis of functionally enriched GO terms based on the application of hypergeometric tests [46]. A bicluster is considered significantly enriched if it has a set of correlated overrepresented terms with Bonferroni corrected p values below \(10^{3}\). Two major observations can be retrieved. First, when focusing on properties of interest (e.g. differential expression), the average significance of biclusters increases as their genes have higher propensity to be functionally coregulated. This trend is observed despite the smaller size of the constrained biclusters. Second, when focusing on rare expression profiles (\(\ge\)3 distinct levels of expression), the average relevance of biclusters slightly decreases as their coregulation is less obvious. Yet, such nontrivial biclusters hold unique properties with potential interest that can be further investigated. To our knowledge, BiC2PAM is the only available biclustering algorithm able to rely on user expectations and other forms of knowledge to focus the search on these nontrivial yet coherent and potentially interesting regions from the input data space.
Conclusions and future work
This work motivates the relevance of constraintguided biclustering for biological data analysis with domain knowledge. To answer this task, we explored the synergies between patternbased biclustering and domaindriven pattern mining. As a result, BiC2PAM algorithm was proposed with two major goals: (1) to learn biclustering models in the presence of an arbitrary number of annotations from knowledge repositories and literature, and (2) to effectively incorporate constraints with nice properties derived from user expectations. BiC2PAM can therefore be applied in the presence of domain knowledge to guarantee a focus on relevant regions and explore potentially high efficiency gains.
We further demonstrated the consistency between domaindriven pattern mining and patternbased biclustering based on the notion of fullpatterns; surveyed the major drawbacks of existing research towards this end; and extended patterngrowth searches with stateoftheart principles to prune the search space by pushing constraints with nice properties deep into the mining process. In particular, we showed the compliance of F2G searches with principles to effectively prune (conditional) FPTrees, and the compliance of IndexSpan searches with principles to effectively prune prefixgrowth structures. These searches were respectively extended to support patternbased biclustering with constant and orderpreserving assumptions.
Meaningful constraints with succinct, monotone, antimonotone and convertible properties were presented for distinct biological tasks (gene expression analysis and network data analysis) in order to focus the search space on lesstrivial yet coherent regions.
Results from synthetic and real data show that the incorporation of background knowledge leads to large efficiency gains that turn the biclustering task tractable for largescale data. We further provide initial evidence of the relevance of the supported types of constraints to discover nontrivial yet meaningful biclusters in expression and network data with heightened biological significance.
Four major directions are identified for future work. First, the extension of the proposed contributions towards classification tasks based on the discriminative properties of biclusters in labeled data contexts. Second, an indepth systematization of constraints with nice properties across biological data domains, including a structured view on their relevance for omic, genomewide and chemical data analysis. Third, a broader quantification of the impact of incorporating constraints across these data domains. Finally, the extension of the proposed framework for the tasks of biclustering time series data and triclustering multivariate time series data in the presence of temporal constraints.
Data and software availability
The datasets and BiC2PAM software are available in http://web.ist.utl.pt/rmch/software/bic2pam/.
Notes
 1.
Biclustering involves combinatorial optimization to select and group rows and columns and it is known to be a NPhard problem (proven by mapping the problem of finding maximum edge (bi)clique in a bipartite graph into the problem of finding dense biclusters with maximum size [2, 10]). The problem complexity increases for nonbinary data contexts and when elements are allowed to participate in more than one bicluster (nonexclusive structure) and in no bicluster at all (nonexhaustive structure).
 2.
Datasets available in http://web.ist.utl.pt/rmch/software/bic2pam/.
Abbreviations
 BicNET:

Biclustering NETworks (algorithm)
 Bic2PAM:

BiClustering with Constraints using PAttern Mining (algorithm)
 BicPAM:

BiClustering using PAttern Mining (algorithm)
 BicSPAM:

Biclustering using Sequential PAttern Mining (algorithm)
 BiModule:

Biclustering Modules (algorithm)
 BiP:

Biclustering Plaid models (algorithm)
 DeBi:

Differentially expressed Biclustering (algorithm)
 F2G:

Full Frequentpattern Growth
 FIM:

Frequent Itemset Mining
 FP:

Frequent Pattern
 GO:

Gene Ontology
 SPM:

Sequential Pattern Mining
References
 1.
Henriques R, Antunes C, Madeira SC. A structured view on pattern miningbased biclustering. Pattern Recogn. 2015;48(12):3941–58.
 2.
Madeira SC, Oliveira AL. Biclustering algorithms for biological data analysis: a survey. IEEE/ACM Trans Comput Biol Bioinformatics. 2004;1:24–45.
 3.
Henriques R, Madeira SC. BicNET: flexible module discovery in largescale biological networks using biclustering. Algorithms Mol Biol. 2016;11:1–30.
 4.
Fang G, Haznadar M, Wang W, Yu H, Steinbach M, Church TR, Oetting WS, Van Ness B, Kumar V, Highorder SNP combinations associated with complex diseases: efficient discovery, statistical power and functional interactions. Plos One. 2012;7:e33531. doi:10.1371/journal.pone.0033531.
 5.
Guerra I, Cerf L, Foscarini J, Boaventura M, Meira W. Constraintbased search of straddling biclusters and discriminative patterns. JIDM. 2013;4(2):114–23.
 6.
Kuznetsov SO, Poelmans J. Knowledge representation and processing with formal concept analysis. Wiley Interdisc Rev Data Min Knowl Discov. 2013;3(3):200–15.
 7.
Visconti A, Cordero F, Pensa RG. Leveraging additional knowledge to support coherent bicluster discovery in gene expression data. Intell Data Anal. 2014;18(5):837–55.
 8.
Martinez R, Pasquier C, Pasquier N, Martinez R, Pasquier C, Pasquier N. GenMiner: mining informative association rules from genomic data. In BIBM. Washington, D.C.: IEEE CS; 2007.
 9.
Nepomuceno JA, Troncoso A, NepomucenoChamorro IA, AguilarRuiz JS. Integrating biological knowledge based on functional annotations for biclustering of gene expression data. Computer Methods Programs Biomed. 2015;119(3):163–80.
 10.
Peeters R. The maximum edge biclique problem is NPcomplete. Discrete Appl Math. 2003;131(3):651–4.
 11.
Hochreiter S, Bodenhofer U, Heusel M, Mayr A, Mitterecker A, Kasim A, Khamiakova T, Van Sanden S, Lin D, Talloen W, Bijnens L, Göhlmann HWH, Shkedy Z, Clevert DA. FABIA: factor analysis for bicluster acquisition. Bioinformatics. 2010;26(12):1520–7.
 12.
Serin A, Vingron M. DeBi: discovering differentially expressed biclusters using a frequent itemset approach. Algorithms Mol Biol. 2011;6:1–12.
 13.
Okada Y, Okubo K, Horton P, Fujibuchi W. Exhaustive search method of gene expression modules and its application to human tissue data. IAENG Int J Comput Sci. 2007;34:119–26.
 14.
Henriques R, Madeira S. BicPAM: patternbased biclustering for biomedical data analysis. Algorithms Mol Biol. 2014;9:27.
 15.
Pei J, Han J. Can we push more constraints into frequent pattern mining? In KDD. New York: ACM; 2000. p. 350–4.
 16.
Bonchi F, Lucchese C. Extending the stateoftheart of constraintbased pattern discovery. Data Knowl Eng. 2007;60(2):377–99.
 17.
Henriques R, Madeira SC, Antunes C. F2G: efficient discovery of fullpatterns. In ECML/PKDD nfMCP. Prague; 2013.
 18.
Henriques R, Antunes C, Madeira S. Methods for the efficient discovery of large itemindexable sequential patterns. In: Appice A, Ceci M, Loglisci C, Manco G, Masciari E, Ras ZW, editors. New frontiers in mining complex patterns. Lecture Notes in Computer Science, vol 8399. Springer; 2014. p. 100–116.
 19.
Henriques R, Madeira S. BicSPAM: flexible biclustering using sequential patterns. BMC Bioinform. 2014;15:130.
 20.
Henriques R, Madeira S. Biclustering with flexible plaid models to unravel interactions between biological processes. IEEE/ACM Transactions on: Comput Biol Bioinform; 2015.12;738–752
 21.
Okada Y, Fujibuchi W, Horton P. A biclustering method for gene expression module discovery using closed itemset enumeration algorithm. IPSJ Trans Bioinform. 2007;48(SIG5):39–48.
 22.
Henriques R, Madeira SC. BicNET: efficient biclustering of biological networks to unravel nontrivial modules. In: Algorithms in bioinformatics (WABI), LNCS. Berlin: SpringerVerlag; 2015.
 23.
Marriott K, Stuckey P. Programming with constraints: an introduction. adaptive computation and machine. Cambridge: MIT Press; 1998.
 24.
Pei J, Han J. Constrained frequent pattern mining: a patterngrowth view. SIGKDD Explor Newslett. 2002;4:31–9.
 25.
Tan PN, Kumar V, Srivastava J. Selecting the right interestingness measure for association patterns. In: Proceedings of the eighth ACM SIGKDD international conference on Knowledge discovery and data mining, KDD ’02. New York: ACM; 2002. p. 32–41.
 26.
Alves R, RodríguezBaena DS, AguilarRuiz JS. Gene association analysis: a survey of frequent pattern mining from gene expression data. Briefings Bioinform. 2010;11(2):210–24.
 27.
Pei J, Han J, Wang W. Constraintbased sequential pattern mining: the patterngrowth methods. J Intell Inf Syst. 2007;28(2):133–60.
 28.
Mouhoubi K, Létocart L, Rouveirol C. A knowledgedriven biclustering method for mining noisy datasets. In: Neural information processing. Berlin:Springer; 2012. p. 585–93.
 29.
Henriques R, Antunes C, Madeira S. Generative modeling of repositories of health records for predictive tasks. Data Min Knowl Discov. 2015;29(4):999–1032. doi:10.1007/s1061801403857.
 30.
Besson J, Robardet C, De Raedt L, Boulicaut JF. Mining bisets in numerical data. In: Knowledge discovery in inductive databases. Berlin:Springer; 2007. p. 11–23.
 31.
Ng RT, Lakshmanan LVS, Han J, Pang A. Exploratory mining and pruning optimizations of constrained associations rules. SIGMOD R. 1998;27(2):13–24.
 32.
Khiari M, Boizumault P, Crémilleux B. Constraint programming for mining nary patterns. In: Principles and practice of constraint programming. Berlin: Springer; 2010. p. 552–67.
 33.
Bonchi F, Goethals B. FPBonsai: the art of growing and pruning small FPtrees. In: Dai H, Srikant R, Zhang C, editors. Advances in knowledge discovery and data mining. Berlin Heidelberg: Springer; 2004. p. 155–60.
 34.
Bonchi F, Giannotti F, Mazzanti A, Pedreschi D. ExAnte: a preprocessing method for frequentpattern mining. IEEE Intell Syst. 2005;20(3):25–31.
 35.
Srikant R, Vu Q, Agrawal R. Mining association rules with item constraints. KDD. 1997;97:67–73.
 36.
Wang K, He Y, Han J. Pushing support constraints into association rules mining. IEEE Trans Knowl Data Eng. 2003;15(3):642–58.
 37.
Bayardo RJ, Agrawal R, Gunopulos D. Constraintbased rule mining in large, dense databases. In: 15th international conference on data engineering. New York: IEEE; 1999. p. 188–97.
 38.
Baralis E, Cagliero L, Cerquitelli T, Garza P. Generalized association rule mining with constraints. Inf Sci. 2012;194:68–84.
 39.
Srikant R, Agrawal R. Mining sequential patterns: generalizations and performance Improvements. In: Proceedings of the 5th international conference on extending database technology: advances in database technology, EDBT ’96. London: SpringerVerlag; 1996. p. 3–17.
 40.
Mannila H, Toivonen H, Verkamo AI. Discovery of frequent episodes in event sequences. Data Min Knowl Discov. 1997;1(3):259–89.
 41.
Garofalakis MN, Rastogi R, Shim K. SPIRIT: sequential pattern mining with regular expression constraints. VLDB. 1999;99:7–10.
 42.
Pei J, Han J, Wang W. Mining sequential patterns with constraints in large databases. In: Proceedings of the eleventh international conference on information and knowledge management. New York: ACM; 2002. p. 18–25.
 43.
Antunes C, Oliveira AL. Generalization of patterngrowth methods for sequential pattern mining with gap constraints. In: Machine learning and data mining in pattern recognition. Berlin: Springer; 2003. p. 239–51.
 44.
Han J, Cheng H, Xin D, Yan X. Frequent pattern mining: current status and future directions. Data Min Knowl Discov. 2007;15:55–86.
 45.
Mabroukeh NR, Ezeife CI. A taxonomy of sequential pattern mining algorithms. ACM Comput Surv. 2010;43:3:1–41.
 46.
Martin D, Brun C, Remy E, Mouren P, Thieffry D, Jacq B. GOToolBox: functional analysis of gene datasets based on gene ontology. Gen Biol. 2004;12:101.
 47.
MacPherson JI, Dickerson J, Pinney J, Robertson D. Patterns of HIV1 protein interaction identify perturbed hostcellular subsystems. PLoS Comput Biol. 2010;6(7):e1000863.
 48.
Mukhopadhyay A, Maulik U, Bandyopadhyay S. A novel biclustering approach to association rule mining for predicting HIV1human protein interactions. PLoS One. 2012;7(4):e32289.
 49.
Henriques R. Learning from highdimensional data using local descriptive models. PhD thesis, Instituto Superior Tecnico, Universidade de Lisboa, Lisboa; 2016.
 50.
Rosenwald A. dlblc team: the use of molecular profiling to predict survival after chemotherapy for diffuse largeBcell lymphoma. N Engl J Med. 2002;346(25):1937–47.
 51.
Lee W, Tillo D, Bray N, Morse RH, Davis RW, Hughes TR, Nislow C. A highresolution atlas of nucleosome occupancy in yeast. Nat Genet. 2007;39(10):1235–44.
 52.
Gasch AP, Spellman PT, Kao CM, CarmelHarel O, Eisen MB, Storz G, Botstein D, Brown PO. Genomic expression programs in the response of yeast cells to environmental changes. Mol Biol Cell. 2000;11(12):4241–57.
 53.
Szklarczyk D, Franceschini A, Wyder S, Forslund K, Heller D, HuertaCepas J, Simonovic M, Roth A, Santos A, Tsafou KP, et al. STRING v10: protein–protein interaction networks, integrated over the tree of life. Nucl Acids Res. 2015;43:D447–52.
 54.
Gasch AP, WernerWashburne M. The genomics of yeast responses to environmental stress and starvation. Funct Integr Genom. 2002;2(4–5):181–92.
Authors’ contributions
RH designed the algorithms under the close supervision of SCM. Both authors revised the final manuscript. Both authors read and approved the final manuscript.
Competing interests
The authors declare that they have no competing interests.
Ethical approval and consent to participate
Not Applicable. The manuscript does not report new studies involving any animal or human data or tissue.
Funding and acknowledgments
This work was supported by Fundação para a Ciência e Tecnologia under the project Neuroclinomics2 PTDC/EEISII/1937/2014, InescID plurianual with reference UID/CEC/50021/2013, the research Grant SFRH/BD/75924/2011 to RH, and the sabbatical leave Grant SFRH/BSAB/1427/2014 to SCM. SCM was also partially funded by the EURIAS Fellowship Programme and the European Commission (MarieSklodowskaCurie actions CoFUND ProgrammeFP7) through a grant for a junior fellowship position at Istituto di Studi Avanzati, University of Bologna, Italy.
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Appendix: Native constraints
Appendix: Native constraints
In addition to the incorporation of functional annotations and specification of constraints with properties of interest, further possibilities can be explored within BiC2PAM to guarantee its ability to learn biclustering solutions with customizable structure, coherency and quality in accordance with domain knowledge. Below we list a set of native constraints to this end that are effectively incorporated within BiC2PAM by adapting the parameters that control its behavior along its preprocessing, mining, postprocessing steps.
Relevant constraints provided in the preprocessing step include:

Minimum coherency strength of the target biclusters (Definition 2). Decreasing the coherency strength (increasing the number of symbols) reduces the allowed deviations from value expectations and it is often associated with solutions composed by a higher number of smaller biclusters;

Tolerance to noise \(\eta _{ij}\) (Definition 2). This constraint is used to adjust the behavior of BiC2PAM in the presence of noise, missing values or discretization drawbacks. BiC2PAM enables the possibility to assign a parameterizable number of symbols to a given data element when its value is near a boundary of discretization. By assigning two or more symbols guarantees a higher robustness to noise (proof in [14]).
Relevant constraints provided in the mining step include:

Coherency assumption and orientation: Currently, BiC2PAM supports the selection of constant, additive, multiplicative, symmetric, orderpreserving and plaid models with coherency on rows or columns. An indepth view on the relevance of nonconstant coherency assumptions for expression and network data analysis was previously provided in [14, 19, 20, 22].

Minimum pattern length and/or support (minimum number of columns and/or rows in the bicluster).

Pattern representation: simple (all coherent biclusters), closed (all maximal biclusters), or maximal (solutions with a compact number of biclusters with a preference towards a high number of columns).

Stopping criteria: minimum number of biclusters able to satisfy the inputted constraints, or minimum area of the input matrix covered by the discovered valid biclusters.
Understandably, constraints addressed at the postprocessing stage are not desirable since they are not able to seize major efficiency gains. Nevertheless, BiC2PAM supports three key types of constraints that could imply additional computational costs, but are addressed with heightened efficiency: (1) maximum percentage of noisy and missing elements per bicluster (based on merging procedures [14]), (2) minimum homogeneity of the target biclusters (using extension and reduction procedures with a parameterizable merit function [14]) and (3) minimum dissimilarity criteria to guarantee compact outputs.
Previous work from Henriques and Madeira [1, 14, 19, 20, 22] provide an indepth description of how patternbased biclustering algorithms implement this wideset of customization possibilities.
The listed native constraints can be specified in declarative form. As such, BiC2PAM provides the possibility to affect structural aspects of its outputs with sharp usability.
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Henriques, R., Madeira, S.C. BiC2PAM: constraintguided biclustering for biological data analysis with domain knowledge. Algorithms Mol Biol 11, 23 (2016). https://doi.org/10.1186/s1301501600855
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Keywords
 Association Rule
 Regular Expression
 Pattern Mining
 Efficiency Gain
 Nice Property