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Misassembly detection using paired-end sequence reads and optical mapping data

Motivation: A crucial problem in genome assembly is the discovery and correction of misassembly errors in draft genomes. We develop a method called misSEQuel that enhances the quality of draft genomes by identifying misassembly errors and their breakpoints using paired-end sequence reads and optical...

詳細記述

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書誌詳細
出版年:Bioinformatics
主要な著者: Muggli, Martin D., Puglisi, Simon J., Ronen, Roy, Boucher, Christina
フォーマット: Artigo
言語:Inglês
出版事項: Oxford University Press 2015
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4542784/
https://ncbi.nlm.nih.gov/pubmed/26072512
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btv262
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