Skip to main content

Correction: Constructing founder sets under allelic and non-allelic homologous recombination

The Original Article was published on 29 September 2023


Correction: Algorithms for Molecular Biology (2023) 18:15 https://doi.org/10.1186/s13015-023-00241-3


The Additional file 1 which originally published contained errors. It has now been replaced with the correct file.

The original article [1] has been corrected.

Reference

  1. Bonnet K, Marschall T, Doerr D. Constructing founder sets under allelic and non-allelic homologous recombination. Algorithms Mol Biol. 2023;18:15. https://doi.org/10.1186/s13015-023-00241-3.

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Tobias Marschall or Daniel Doerr.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Additional file 1: Figure S1

. Reduction in the number of recombinations following minimization. The plots show the total number of recombinations before (blue dots) and after (red dots) minimization, as a function of each simulation parameter. Figure S2. Number of recombinations minimization benchmarks. Runtime (upper panels) and peak PSS (lower panels) as a function of the number of haplotypes (left) and the ratio of inverted duplications (right). Figure S3. Flow computation performance with a variable ratio of inversions. Runtime (left) and memory usage (right) as a function of this parameter. Figure S4. Visualization of a solution to the minimization problem on the 1p36.13 locus. The gray bars correspond to the graph’s nodes, labeled 1 to 8. The founder sequence (>1>2>3<7>5>2>3<4>5>5<6<4<3>7<3<2<4>5>6<5>4<5<4<3<2>7<3>6>7<3<4<3<2>6<4>3>2>7>8) is traced from top to bottom. A slanted line indicates the underlying node being traversed; if slanted rightwards, traversal is in forward direction, and if slanted leftwards, traversal is in reverse direction. Colors correspond to different haplotypes. The haplotype sequence is: EUR-HG00171-h2, AFR-NA19036-h1, SAS-GM20847-h2, AFR-HG03065-h2, AFR-NA19036-h1, AFR-NA19036-h1, AMR-HG01573-h2, AFR-HG02011-h2, AFR-HG03371-h2, SAS-HG03683-h2. Recombinations are marked with a star. Table S1. Sorted haplotype marker sequences used for analyzing the 1p36.13 locus.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Bonnet, K., Marschall, T. & Doerr, D. Correction: Constructing founder sets under allelic and non-allelic homologous recombination. Algorithms Mol Biol 18, 20 (2023). https://doi.org/10.1186/s13015-023-00244-0

Download citation

  • Published:

  • DOI: https://doi.org/10.1186/s13015-023-00244-0