Highnam, GarethFranck, Christopher T.Martin, AndyStephens, CalvinPuthige, AshwinMittelman, David2019-04-152019-04-152013-01NVIDIA Foundation’s ‘Compute the Cure’ program (to D.M.). Funding for open access charge: NIH.0305-1048http://hdl.handle.net/10919/88962Repetitive sequences are biologically and clinically important because they can influence traits and disease, but repeats are challenging to analyse using short-read sequencing technology. We present a tool for genotyping microsatellite repeats called RepeatSeq, which uses Bayesian model selection guided by an empirically derived error model that incorporates sequence and read properties. Next, we apply RepeatSeq to high-coverage genomes from the 1000 Genomes Project to evaluate performance and accuracy. The software uses common formats, such as VCF, for compatibility with existing genome analysis pipelines. Source code and binaries are available at http://github.com/adaptivegenome/repeatseq.7 pagesapplication/pdfen-USCreative Commons Attribution 4.0 Internationalrepeat instabilitysequencing dataread alignmentdisordersmutationsevolutionformatArticle - Refereedhttps://doi.org/10.1093/nar/gks981411230909811362-4962