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PMID: 25658651 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

WhatsHap: Weighted Haplotype Assembly for Future-Generation Sequencing Reads.

Patterson M, Marschall T, Pisanti N, van Iersel L, Stougie L, Klau GW, Schönhuth A

Abstract

The human genome is diploid, which requires assigning heterozygous single nucleotide polymorphisms (SNPs) to the two copies of the genome. The resulting haplotypes, lists of SNPs belonging to each copy, are crucial for downstream analyses in population genetics. Currently, statistical approaches, which are oblivious to direct read information, constitute the state-of-the-art. Haplotype assembly, which addresses phasing directly from sequencing reads, suffers from the fact that sequencing reads of the current generation are too short to serve the purposes of genome-wide phasing. While future-technology sequencing reads will contain sufficient amounts of SNPs per read for phasing, they are also likely to suffer from higher sequencing error rates. Currently, no haplotype assembly approaches exist that allow for taking both increasing read length and sequencing error information into account. Here, we suggest WhatsHap, the first approach that yields provably optimal solutions to the weighted minimum error correction problem in runtime linear in the number of SNPs. WhatsHap is a fixed parameter tractable (FPT) approach with coverage as the parameter. We demonstrate that WhatsHap can handle datasets of coverage up to 20×, and that 15× are generally enough for reliably phasing long reads, even at significantly elevated sequencing error rates. We also find that the switch and flip error rates of the haplotypes we output are favorable when comparing them with state-of-the-art statistical phasers.

Keywords
algorithms combinatorial optimization dynamic programming haplotypes next generation sequencing
MeSH Terms
Diploidy Genetics, Population/methods Genome, Human/genetics Haplotypes/genetics High-Throughput Nucleotide Sequencing/methods Humans Polymorphism, Single Nucleotide/genetics Sequence Analysis, DNA/methods
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Patterson Murray
1Laboratoire de Biométrie et Biologie Évolutive (LBBE : UMR CNRS 5558), Université de Lyon 1, Villeurbanne, France.
Marschall Tobias
2Center for Bioinformatics, Saarland University, Saarbrücken, Germany. | 3Max Planck Institute for Informatics, Saarbrücken, Germany.
Pisanti Nadia
4Department of Computer Science, University of Pisa, Italy. | 7Erable Team, INRIA.
van Iersel Leo
Stougie Leen
6VU University, Amsterdam, The Netherlands. | 7Erable Team, INRIA.
Klau Gunnar W
6VU University, Amsterdam, The Netherlands. | 7Erable Team, INRIA.
Schönhuth Alexander
Article Info
Journal
Journal of computational biology : a journal of computational molecular cell biology
Abbr.
J Comput Biol
ISSN
1557-8666
Published
2015-06-00
Epub
2015-00-06
Pages
498-509
Language
English
Region
United States
NLM ID
9433358
Subset
IM
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