Phylogenetic comparative assembly
- Peter Husemann^{1, 2}Email author and
- Jens Stoye^{1, 3}
https://doi.org/10.1186/1748-7188-5-3
© Husemann and Stoye; licensee BioMed Central Ltd. 2010
Received: 7 August 2009
Accepted: 4 January 2010
Published: 4 January 2010
Abstract
Background
Recent high throughput sequencing technologies are capable of generating a huge amount of data for bacterial genome sequencing projects. Although current sequence assemblers successfully merge the overlapping reads, often several contigs remain which cannot be assembled any further. It is still costly and time consuming to close all the gaps in order to acquire the whole genomic sequence.
Results
Here we propose an algorithm that takes several related genomes and their phylogenetic relationships into account to create a graph that contains the likelihood for each pair of contigs to be adjacent.
Subsequently, this graph can be used to compute a layout graph that shows the most promising contig adjacencies in order to aid biologists in finishing the complete genomic sequence. The layout graph shows unique contig orderings where possible, and the best alternatives where necessary.
Conclusions
Our new algorithm for contig ordering uses sequence similarity as well as phylogenetic information to estimate adjacencies of contigs. An evaluation of our implementation shows that it performs better than recent approaches while being much faster at the same time.
Background
Today the nucleotide sequences of many genomes are known. In the first genome projects, the process of obtaining the DNA sequence by multi-step clone-by-clone sequencing approaches was costly and tedious. Nowadays, the most common approach for de-novo genome sequencing is whole genome shotgun sequencing[1, 2]. Here, the genome is fragmented randomly into small parts. Each of these fragments is sequenced, for example, with recent high throughput methods [3, 4]. In the next step, overlapping reads are merged with an assembler software into a contiguous string. However, instead of the desired one sequence of the whole genome, often many contigs remain, separated by gaps. The main reasons for these gaps are lost fragments in the fragmentation phase and repeating sequences in the genome. In a process called scaffolding, the relative order of the contigs as well as the size of the gaps between them is estimated. In a subsequent finishing phase the gaps between the contigs are closed with a procedure called primer walking. For the ends of two estimated adjacent contigs, specific primer sequences have to be designed that function as start points for two polymerase chain reactions (PCRs) for Sanger sequencing [5]. These PCRs ideally run towards each other until the sequences overlap. To close a gap completely, new primer pairs have to be generated again and again since the maximum read length for Sanger sequencing is restricted. This makes the process expensive and work intensive. It is thus advisable to reduce the pairs of contigs that have to be considered. Given n contigs and no further information about their order, there are (n^{2}) possibilities to apply primer walking. If the order is known, it suffices to do (n) primer walks to fill the gaps.
An algorithm that estimates a reasonable order for the contigs is thus a good help for sequencing projects. The estimation is usually based on the sequences of closely related species that are assumed to have a high degree of synteny. A few tools have been developed which use one or several related reference genomes to devise an ordering of the contigs: Projector2 [6], for example, is a web service that maps contig ends on a template genome using BLAST [7] or BLAT [8]. Features of Projector2 are an optional repeat masking for contig and template sequences, a visualization of the mapping, and an automated primer-design step for gap-closing purposes. Prior to the automated primer design, difficult regions for primer walking are removed, like, for example, repetitive sequences (phage DNA, IS elements or gene duplications) or sequences with unbalanced GC content. The program OSLay [9] takes a set of BLAST matches between the contigs and a reference sequence or scaffold and computes from this a layout for the contigs. The algorithm minimizes the height differences of so-called local diagonal extensions, which are basically matches from the border of a contig to the reference sequence. The resulting layout is visualized and can be imported into a Consed [10] project to aid gap-closure. Zhao et al. [11] present a method to find an ordering for a set of contigs using several related sequences as references. For each reference genome a fitness matrix is computed giving distances between the contigs, based on their BLAST matches. All matrices are combined into a single fitness matrix to search an optimal path of contig connections with their heuristic PGA (pheromone trail-based genetic algorithm).
Our work in this field commenced when analyzing data from in-house sequencing projects for different species of the Corynebacteria genus. We observed several aspects making it hard to find an ordering of the contigs. Zhao et al. [11] show that poor sequence coverage can be overcome by using multiple reference genomes, but problematic for this approach are major rearrangements in the genomic sequences of more distantly related species. Another challenge are repeating regions in the sequence of the newly sequenced genome. We developed an algorithm that uses the information of all similar regions between a set of contigs and several related reference genomes to estimate an ordering of the contigs. The novel idea is to incorporate the phylogenetic distance of the species in order to alleviate the impact of rearrangements to the ordering. While generating one 'optimal' order of the contigs is the predominant approach to aid the closure of gaps, we propose a more flexible format to describe contig adjacencies that is also capable of dealing with repeating contigs.
The algorithm we present here is based on a simple data structure, the contig adjacency graph, that is introduced in the next section. There we also give an optimal solution for finding a linear ordering of the contigs using this graph. However, a linear ordering is not sufficient to reflect all relations of real contig data. Therefore we propose a heuristic by which the most promising, but not necessarily unique, adjacencies are revealed in a layout graph. In section 'Results and discussion' we show the evaluation of applying our method to real sequencing data and compare the results with those obtained by PGA.
Methods
A natural strategy to devise an 'optimal' linear ordering of the contigs, based on one or several related reference genomes, works in three steps: At first, all similar regions between the contigs and each reference genome are determined. Then a graph is created, containing edge weights that reflect the neighborhood of the contigs. In the last step a weight maximizing path through the graph is calculated, which defines the desired order of the contigs. In the following, we describe these three steps in more detail. In particular, in Section 'Contig adjacency graph', we define a novel edge weight function that incorporates the phylogenetic distance of the involved species.
Matching contigs against a reference
Let Σ ={A, C, G, T} be the alphabet of nucleotides. We denote by Σ* the set of all finite strings over Σ, by |s|:= ℓ the length of string s = s_{1} ... s_{ℓ}, and by s [i, j]:= s_{ i }... s_{ j }with 1 ≤ i ≤ j ≤ ℓ the substring of s that starts at position i and ends at position j. Suppose we are given a set of contigs ={c_{1}, ..., c_{ n }}, c_{ i }∈ Σ*, and a set of already finished reference genomes ℛ ={g_{1}, ..., g_{ m }}, g_{ r }∈ Σ*. The relation of the reference genomes is given by a phylogenetic tree that contains the evolutionary distances of the species. Note that the tree can be generated even if some genomes are not completely assembled yet, for example from 16S-rRNAs. To infer information about the order and orientation of the contigs, these are mapped onto each reference genome by calculating local alignments. Let s = c [s_{ b }, s_{ e }] be a substring of contig c and t = g [t_{ b }, t_{ e }] be a substring of reference genome g. The tuple m = ((s_{ b }, s_{ e }), (t_{ b }, t_{ e })) is called a matching region or simply match if s and t share sufficient sequence similarity. The length of a match, |m|:= t_{ e }-t_{ b }+1, is defined as the length of the covered substring in the reference genome. Sufficient sequence similarity could be defined, for example, by a BLAST hit of significance above a user-defined threshold. Another possibility, that we employ in our implementation, is to use the swift algorithm [12] for matching. It utilizes a q-gram index and provides for each match m the number of exactly matching q-grams, denoted as qhits(m), which can be used as a quality estimation for that match. Note that each contig can have several matches on a reference genome. For s_{ b }> s_{ e }we define c [s_{ b }, s_{ e }] to be the reverse complement of c [s_{ e }, s_{ b }] and call m a reverse match. Further we assume w.l.o.g. that t_{ b }< t_{ e }for all g [t_{ b }, t_{ e }], otherwise we can replace the involved contig sequence by its reverse complement. For brevity of notation, denotes a match between contig c_{ i }∈ and reference genome g_{ r }∈ ℛ, and denotes the (possibly empty) set of all such matches.
If the matches refer to different reference genomes, the distance of their projections is undefined. Note that the term distance is used here in the sense of 'displacement', d is not a metric in the mathematical sense. For example, d is negative if the projected contigs overlap.
Contig adjacency graph
In the following we define the edge-weighted contig adjacency graph = (V, E) that contains for each contig c_{ i }∈ two vertices: l_{ i }as the left connector and r_{ i }as the right connector of contig c_{ i }. The set of vertices V is then defined as V = L ∪ R, where L ={l_{1}, ..., l_{ n }} and R = {r_{1}, ..., r_{ n }}.
The graph is fully connected: E = ( ). We split these edges into two subsets: the intra contig edges I ={{l_{1}, r_{1}}, ..., {l_{ n }, r_{ n }}} which connect for each contig its left and its right connector; and the set of adjacency edges A = E\I that connect the contigs among each other.
A second important aspect that is included in our model are rearrangements between the related species, which can lead to misleading adjacencies of projected contigs. Assuming that between closer related species less rearrangements have taken place, we use the phylogenetic tree distance to weight the match information.
where s is the standard deviation for the size of deletions or insertions. A higher tree distance allows larger insertions and deletions, but scores the reliability of the matches to more distantly related genomes to a lesser degree.
The expected value μ of the second Gaussian distribution is equal to the average size of the lost fragments.
The standard deviations σ_{1} and σ_{2} can be estimated from sequencing projects.
Finding a tour through the graph
The contig adjacency graph with the described edge weights can be used to find a linear ordering of the contigs. This can be achieved by computing a tour through the graph that incorporates all contigs and maximizes the total weight. With minor enhancements of the graph, this becomes equivalent to finding a shortest Hamiltonian cycle.
The modifications are as follows: At first all edge weights have to be converted to distances. This is done by replacing each edge weight w by m - w where m is the maximum weight in the graph. To ensure that each contig is incorporated exactly once, and only in one direction, we add an intermediate node between the left and the right connector of each contig. The modified graph is then defined as = (V', E') with V' = V ∪ {v_{ i }| 1 ≤ i ≤ n} and E' = A ∪ {{l_{ i }, v_{ i }}, {v_{ i }, r_{ i }}| 1 ≤ i ≤ n}. The distance of all edges that lead to an intermediate node v_{ i }is set to 0. It is easy to see that a shortest Hamiltonian cycle in the modified graph defines an ordering as well as the orientation of all contigs, and thus any TSP algorithm can be used to find an optimal linear layout of the contigs.
Fast adjacency discovery algorithm
As described in the previous section, a linear ordering of the contigs, which is optimal with respect to the adjacency edge weights, can be computed using a suitable optimization algorithm. However, our analysis of real data in the results section shows that a linear order of the contigs is not necessarily possible, mainly due to arbitrary placement of repeated or rearranged regions. A method that provides a unique layout where possible, but also points out alternative solutions where necessary, may be more useful in practice. We present an approach following this overall strategy in this section.
The basis of our algorithm is a greedy heuristic for the TSP, known as the multi-fragment heuristic[13], that proceeds as follows: First the edges of the graph are sorted by increasing distance and then added in this order into an initially empty set of path fragments. Whenever an involved node would exceed the maximal degree of two, or if a path fragment would create a cycle, the edge is skipped. The only exception to the latter is the final Hamiltonian cycle of length n.
This best connection first procedure creates multiple low distance path fragments which are merged sooner or later. We chose this approach because it seems natural to incorporate those adjacencies first into an ordering that are most promising to be investigated for gap closure.
The layout graph can be analyzed to make assumptions about repeating contigs and rearrangements. Conflicting edges can give hints about these two problems, whereas the information about unambiguously incorporated contigs can be used to generate primer pairs for gap closure. Displaying also the ambiguities allows to investigate the conflicting connections further. Instead of pinning the result down to a single, possibly wrong, order of the contigs we prefer to output the best possibilities. Nonetheless it should be kept in mind that rearrangements can cause seemingly good adjacencies that do not belong to a correct layout.
Integrating additional information
In sequencing projects often additional information occurs which can be helpful for the scaffolding of a genome. After introducing two of such information types, we outline how they may be incorporated into our approach.
1. Recent protocols for parallel pyrosequencing produce mate pair information. Fragments of a defined size are sequenced from both ends thus providing the approximate distance as well as the orientation of both reads relative to each other. This information simplifies the assembly and sometimes indicates adjacencies of contigs.
2. After an initial assembly of the reads, often fosmid libraries are employed to accomplish the finishing of a genome. Fragments of the genome with a size between 35 and 40 kb are used as inserts for the fosmids in order to sequence the ends of each inserted fragment. If those end sequences can be mapped to different contigs, it is possible to infer the distance and orientation of contigs towards each other. Fosmid libraries have the additional advantage that they can be used for primer walking even if the gaps between the contigs exceed the usual size to do primer walking on the genome. But of course this advantage is paid for with a high amount of work to create the library.
The information from mate pairs, fosmid libraries or on a larger scale even radiation hybrid maps can be included into our approach by modifying the weights of the computed contig adjacency graph. This influences also the predicted adjacencies in the layout graph which is the outcome of our algorithm. If expert information indicates that two contigs are not adjacent, it suffices to set the appropriate edge weight to zero. This contig connection will not occur in the result afterwards. On the contrary, if for example fosmid end sequencing shows that two contigs are adjacent and quite close, the incorporation of that edge into the layout graph can be forced by setting the corresponding edge weight to the maximum weight of the graph.
Results and discussion
Datasets
Contig sets
Contig Organism | # Contigs | Total Length | N50 Contig Size |
---|---|---|---|
C. aurimucosum ATCC 700975 | 108 | 2 716 204 bp | 96 704 bp |
C. kroppenstedtii DSM 44385 | 9 | 2 434 935 bp | 546 376 bp |
C. urealyticum DSM 7109 | 69 | 2 294 755 bp | 86 391 bp |
Reference genomes
Reference Organism | Sequence Length | Accession Nr. |
---|---|---|
C. aurimucosum ATCC 700975 | 2 790 189 bp | NC_012590 |
C. diphtheriae NCTC 13129 | 2 488 635 bp | NC_002935 |
C. efficiens YS-314 | 3 147 090 bp | NC_004369 |
C. glutamicum ATCC 13032 | 3 282 708 bp | NC_006958 |
C. jeikeium K411 | 2 462 499 bp | NC_007164 |
C. jeikeium K411 plasmid pKW4 | 14 323 bp | NC_003080 |
C. kroppenstedtii DSM 44385 | 2 446 804 bp | NC_012704 |
C. urealyticum DSM 7109 | 2 369 219 bp | NC_010545 |
Experimental setup
In the following we address the outcome of three different experiments: At first we used PGA [11] to order the contigs, given the finished genome as reference. Secondly, we applied OSLay [9] and Projector2 [6] to find an ordering of the contigs, each time with the closest genome as reference sequence. Finally, as an evaluation of our proposed method, we compare the performance of PGA and our implementation treecat using all reference genomes except for the one to be finished.
In each experiment, the mentioned programs were run to devise an ordering of the contigs. The output was then compared to the reference order. We counted all connections which also occur in the corresponding reference order as true positives (TP), all others as false positives (FP). From these values we calculated the sensitivity (also called true positive rate, , where P is the number of connections in the reference order) as well as the precision (also called positive predictive value, ). All four values are given in the result tables for each experiment. For PGA, which is a randomized algorithm, the results were often varying, so we give the mean values for applying the program 20 times. Additionally the best result, which yielded the highest TP while having the lowest FP, is given in parentheses.
Assessing the difficulty of comparative assembly
Uniqueness of a linear order
Our first experiment serves as a demonstration how difficult it is to order the contigs of the given datasets. PGA was applied on each contig set with only one reference, the already finished genome of the contigs, which ought to provide the 'perfect' information.
A run of PGA proceeds as follows: First BLAST is used to match the contigs on each given genome. After that PGA computes five paths for the contigs that optimize a fitness matrix which is comparable to our contig adjacency graph. For that purpose a genetic algorithm is used, possibly giving different connections with each run. The connections of all five paths are included into the result together with a weight giving the percentage how often this connection occurred.
PGA results - Perfect reference
PGA | ||||
---|---|---|---|---|
Organism | TP | FP | TPR | PPV |
C. aurimucosum | 19.3 (20) | 44.2 (40) | 0.18 (0.19) | 0.30 (0.33) |
C. kroppenstedtii | 3.0 (3) | 3.0 (3) | 0.33 (0.33) | 0.50 (0.50) |
C. urealyticum | 24.2 (25) | 33.4 (31) | 0.35 (0.36) | 0.42 (0.45) |
Single reference based ordering
The second experiment was designed to underline that the incorporation of several related genomes is favorable to the use of only a single reference sequence. Therefore, we applied OSLay [9] and Projector2 [6] on our datasets using the closest phylogenetic neighbor as reference sequence.
To generate the OSLay results, the contigs were mapped using nucmer from the MUMMER package [20]. We used OSLay then to compute an optimal syntenic layout of the contigs using the standard parameters of the implementation. The adjacencies were finally extracted from the supercontigsList.x.txt files. The Projector2 results were generated using its web-service with standard parameters. The matching was performed by running BLAT on the server.
OSLay and Projector2 results
OSLay | Projector2 | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
Organism | Closest Reference | TP | FP | TPR | PPV | TP | FP | TPR | PPV | |
C. aurimucosum | C. glutamicum | 0 | 1 | 0.00 | 0.00 | 10 | 20 | 0.09 | 0.33 | |
C. kroppenstedtii | C. jeikeium | 0 | 0 | 0.00 | undef. | 1 | 2 | 0.11 | 0.33 | |
C. urealyticum | C. jeikeium | 6 | 6 | 0.09 | 0.50 | 8 | 18 | 0.12 | 0.31 |
Evaluation
Implementation treecat
We implemented our proposed algorithm in Java. The software treecat (tree based contig arrangement tool) contains a re-implementation of the fast local alignment algorithm swift[12], the contig adjacency graph creation, a branch and bound exact TSP algorithm, and the fast layout graph heuristic described in section 'Fast adjacency discovery algorithm'. The software is open source (GPL) and available within the Comparative Genomics - Contig Arrangement Toolsuite (cg-cat, http://bibiserv.techfak.uni-bielefeld.de/cg-cat) on the Bielefeld Bioinformatics Server (BiBiServ). Input to treecat are the FASTA [21] sequences of the contigs and of the related references as well as a phylogenetic tree in Newick format. Each reference can consist of several sequences, for example several chromosomes. When the algorithm is run, first all matches from the contigs to each reference are computed. For the following results, matches were considered to have a minimal length of 64 bases and a maximum error rate of 8%. The matches are cached which allows a visualization like in Figure 5 and avoids a new computation if subsequent steps are re-run with different parameters. As the second step, after the matching, the contig adjacency graph is constructed as defined in the Methods section. The following (empirically estimated) parameters were used for the scoring function (1) to compute the results: The standard deviation of the insertion/deletion size was set to σ_{1} = 10 000 bases and the expected lost fragment size to μ = 2 000 bases with a standard deviation of σ_{2} = 1 000 bases. The lost fragment weighting factor φ was set to 0.1. In the last step, the computed adjacency graph is used to devise the contig layout graph which can then be visualized with the open source software package GraphViz [22].
Comparison of PGA and treecat
PGA and treecat results using multiple references
PGA | treecat | ||||||||
---|---|---|---|---|---|---|---|---|---|
Organism | TP | FP | TPR | PPV | TP | FP | TPR | PPV | |
C. aurimucosum | 14.5 (16) | 66.5 (70) | 0.13 (0.15) | 0.18 (0.19) | 17 | 66 | 0.16 | 0.20 | |
C. kroppenstedtii | 2.0 (2) | 4.0 (4) | 0.22 (0.22) | 0.33 (0.33) | 3 | 6 | 0.33 | 0.33 | |
C. urealyticum | 20.9 (25) | 72.5 (76) | 0.30 (0.36) | 0.22 (0.25) | 27 | 70 | 0.39 | 0.28 |
PGA and treecat results using multiple references: Times
PGA | treecat | ||||
---|---|---|---|---|---|
Organism | Matching | Layouting | Matching | Layouting | |
C. aurimucosum | 436.2 s | 184.1 s | 104.4 s | 0.9 s | |
C. kroppenstedtii | 208.4 s | 25.6 s | 83.4 s | 0.4 s | |
C. urealyticum | 458.8 s | 161.5 s | 100.0 s | 1.2 s |
Comparing the graphs of both programs visually gives the impression that the treecat result is a little less cluttered. This impression becomes even stronger if all small nodes in gray are ignored.
There are a few details to mention when investigating the resulting graphs for ordering the C. urealyticum contigs. PGA's graph contains a connection placing contig 26 next to contig 52 which is obviously incorrect. Our approach does not show this connection. Manual inspection shows that this is due to the evolutionary distances that we incorporate for the edge scoring since phylogenetically closer genomes do not contain this adjacency. This is further supported by the fact that the connection is also not present when PGA uses the 'perfect' reference, see Figure 6.
In our graph the connection from contig 4 to contig 56 as well as the connection from contig 7 to contig 58 has a high score but is not correct. This is explainable due to the big inversion, see Figure 5(a), in the C. jeikeium genome which is the next phylogenetic neighbor to C. urealyticum and therefore has a high influence on our result.
Further investigation of the treecat result in Figure 8 gives additional details: For the contigs 12 to 26, an almost unique path can be observed that orders most of the inner contigs. Repeating contigs like 27 or 62 show a star-like adjacency pattern which can be explained by different adjacencies of the corresponding repeat occurrences. However, there are also larger non-repeating contigs, like contig 12, that show such a star pattern. In this case several different repeating contigs neighbor this contig on different references. The graph shows a double connection 46 to 47, which can be explained by a repeating reverse complement match of a part of contig 46 that lies once before contig 47 and once behind it. This results in a high edge weight for the left connectors {l_{46}, l_{47}}, as well as the right connectors {r_{46}, r_{47}} of these contigs. Some connections, like 52 to 55, seem to imply missing contigs, but further investigation reveals that contigs 53 and 54 are partially repeating contigs which fit between the mentioned contigs but as well next to other contigs. There are adjacencies in the layout graph that have a high difference in the rank of the reference order. For example the connection from contig 16 to 44 seems erroneous but it can be explained by a 1.5 kb repeating substring of contig 44. Similar observations can be made in several other places.
Conclusions
In this paper, we presented an algorithm that orders a set of contigs, given several related reference genomes and a phylogenetic tree of the involved species. In particular, we proposed a more flexible output for the ordering of contigs since our results demonstrate that for real world data the search for one linear optimal ordering of the contigs is not feasible. Consequently, our algorithm allows alternative connections in a layout which is necessary because of repeating regions and rearrangements between the species. Secondly, we introduced a novel scoring function for the contig adjacency estimation that is biologically motivated in two ways: It contains a sophisticated weighting scheme for the distances of projected contigs and it integrates the phylogenetic distances of the species to alleviate the effects caused by rearrangements. An evaluation of our algorithm shows that its implementation treecat is considerably faster than a recent approach from the literature while it is at the same time generating better results. We believe that with our approach of including phylogenetic information into the problem of contig layouting, we have gone one step further in using all available information for this important task within genome finishing.
Nevertheless, in sequencing projects, often additional information emerges which is not yet included in our approach. For example, information derived from mate pairs, fosmid libraries or radiation hybrid maps might give valuable hints on the orientation and the distance of contigs while not being biased by evolutionary events. Concerning the phylogenetic tree, rearrangements between the genomes were not predicted by the methods presented in this paper. This leads to ambiguous information for the ordering of contigs and thus to weak or misleading adjacency scores which need to be curated manually. A strategy for the discovery of rearrangements is thus desired in future work. Furthermore, due to horizontal gene transfer some regions of a genome can have different evolutionary histories than others. Detecting such regions and treating them in a special way might be advisable in an even more sophisticated approach.
Declarations
Acknowledgements
The authors wish to thank Christian Rückert, Susanne Schneiker-Bekel, Eva Trost, and Andreas Tauch for the sequence data, Jochen Blom and Burkhard Linke for the phylogenetic tree, and Travis Gagie and Roland Wittler for helpful discussions.
A preliminary version of this work appeared in the WABI'09 proceedings.
Authors’ Affiliations
References
- Staden R: A strategy of DNA sequencing employing computer programs. Nucleic Acids Res. 1979, 6 (7): 2601-2610. 10.1093/nar/6.7.2601PubMedPubMed CentralView ArticleGoogle Scholar
- Anderson S: Shotgun DNA sequencing using cloned DNase I-generated fragments. Nucleic Acids Res. 1981, 9 (13): 3015-3027. 10.1093/nar/9.13.3015PubMedPubMed CentralView ArticleGoogle Scholar
- Mardis ER: The impact of next-generation sequencing technology on genetics. Trends Genet. 2008, 24 (3): 133-141.PubMedView ArticleGoogle Scholar
- Pop M, Salzberg SL: Bioinformatics challenges of new sequencing technology. Trends Genet. 2008, 24 (3): 142-149.PubMedPubMed CentralView ArticleGoogle Scholar
- Sanger F, Nicklen S, Coulson AR: DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci USA. 1977, 74 (12): 5463-5467. 10.1073/pnas.74.12.5463PubMedPubMed CentralView ArticleGoogle Scholar
- van Hijum SAFT, Zomer AL, Kuipers OP, Kok J: Projector 2: contig mapping for efficient gap-closure of prokaryotic genome sequence assemblies. Nucleic Acids Res. 2005, 33: W560-W566. 10.1093/nar/gki356PubMedPubMed CentralView ArticleGoogle Scholar
- Altschul S, Gish W, Miller W, Myers E, Lipman D: Basic local alignment search tool. J Mol Biol. 1990, 215: 403-410.PubMedView ArticleGoogle Scholar
- Kent WJ: BLAT - The BLAST-Like Alignment Tool. Genome Res. 2002, 12 (4): 656-664.PubMedPubMed CentralView ArticleGoogle Scholar
- Richter DC, Schuster SC, Huson DH: OSLay: optimal syntenic layout of unfinished assemblies. Bioinformatics. 2007, 23 (13): 1573-1579. 10.1093/bioinformatics/btm153PubMedView ArticleGoogle Scholar
- Gordon D, Abajian C, Green P: Consed: a graphical tool for sequence finishing. Genome Res. 1998, 8 (3): 195-202.PubMedView ArticleGoogle Scholar
- Zhao F, Zhao F, Li T, Bryant DA: A new pheromone trail-based genetic algorithm for comparative genome assembly. Nucleic Acids Res. 2008, 36 (10): 3455-3462. 10.1093/nar/gkn168PubMedPubMed CentralView ArticleGoogle Scholar
- Rasmussen KR, Stoye J, Myers EW: Efficient q-Gram Filters for Finding All epsilon-Matches over a Given Length. J Comp Biol. 2006, 13 (2): 296-308. 10.1089/cmb.2006.13.296. 10.1089/cmb.2006.13.296View ArticleGoogle Scholar
- Bentley JL: Fast Algorithms for Geometric Traveling Salesman Problems. Informs J Comp. 1992, 4 (4): 387-411. 10.1287/ijoc.4.4.387. 10.1287/ijoc.4.4.387View ArticleGoogle Scholar
- Tauch A, Trost E, Tilker A, Ludewig U, Schneiker S, Goesmann A, Arnold W, Bekel T, Brinkrolf K, Brune I, Götker S, Kalinowski J, Kamp PB, Lobo FP, Viehoever P, Weisshaar B, Soriano F, Dröge M, Pühler A: The lifestyle of Corynebacterium urealyticum derived from its complete genome sequence established by pyrosequencing. J Biotechnol. 2008, 136 (1-2): 11-21. 10.1016/j.jbiotec.2008.02.009PubMedView ArticleGoogle Scholar
- Tauch A, Schneider J, Szczepanowski R, Tilker A, Viehoever P, Gartemann KH, Arnold W, Blom J, Brinkrolf K, Brune I, Götker S, Weisshaar B, Goesmann A, Dröge M, Pühler A: Ultrafast pyrosequencing of Corynebacterium kroppenstedtii DSM44385 revealed insights into the physiology of a lipophilic corynebacterium that lacks mycolic acids. J Biotechnol. 2008, 136 (12): 22-30. 10.1016/j.jbiotec.2008.03.004PubMedView ArticleGoogle Scholar
- Wheeler DL, Chappey C, Lash AE, Leipe DD, Madden TL, Schuler G, Tatusova TA, Rapp BA: Database resources of the National Center for Biotechnology Information. Nucleic Acids Res. 2000, 28: 10-14. 10.1093/nar/28.1.10PubMedPubMed CentralView ArticleGoogle Scholar
- Benson DA, Karsch-Mizrachi I, Lipman DJ, Ostell J, Rapp BA, Wheeler DL: GenBank. Nucleic Acids Res. 2000, 28: 15-18. 10.1093/nar/28.1.15PubMedPubMed CentralView ArticleGoogle Scholar
- Blom J, Albaum SP, Doppmeier D, Pühler A, Vorhölter FJ, Goesmann A: EDGAR: A software framework for the comparative analysis of microbial genomes. BMC Bioinformatics. 2009, 10: 154- 10.1186/1471-2105-10-154PubMedPubMed CentralView ArticleGoogle Scholar
- Saitou N, Nei M: The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol. 1987, 4 (4): 406-425.PubMedGoogle Scholar
- Kurtz S, Phillippy A, Delcher AL, Smoot M, Shumway M, Antonescu C, Salzberg SL: Versatile and open software for comparing large genomes. Genome Biol. 2004, 5 (2): R12-10.1186/gb-2004-5-2-r12PubMedPubMed CentralView ArticleGoogle Scholar
- Pearson WR, Lipman DJ: Improved tools for biological sequence comparison. Proc Natl Acad Sci USA. 1988, 85 (8): 2444-2448. 10.1073/pnas.85.8.2444PubMedPubMed CentralView ArticleGoogle Scholar
- Gansner ER, North SC: An Open Graph Visualization System and Its Applications to Software Engineering. Softw Pract Exper. 1999, 30: 1203-1233. 10.1002/1097-024X(200009)30:11<1203::AID-SPE338>3.0.CO;2-N.View ArticleGoogle Scholar
- Fredslund J: PHY.FI: fast and easy online creation and manipulation of phylogeny color figures. BMC Bioinformatics. 2006, 7: 315-10.1186/1471-2105-7-315PubMedPubMed CentralView ArticleGoogle Scholar
Copyright
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.