Tigmint: correcting assembly errors using linked reads from large molecules

BACKGROUND: Genome sequencing yields the sequence of many short snippets of DNA (reads) from a genome. Genome assembly attempts to reconstruct the original genome from which these reads were derived. This task is difficult due to gaps and errors in the sequencing data, repetitive sequence in the und...

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發表在:BMC Bioinformatics
Main Authors: Jackman, Shaun D., Coombe, Lauren, Chu, Justin, Warren, Rene L., Vandervalk, Benjamin P., Yeo, Sarah, Xue, Zhuyi, Mohamadi, Hamid, Bohlmann, Joerg, Jones, Steven J.M., Birol, Inanc
格式: Artigo
語言:Inglês
出版: BioMed Central 2018
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在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC6204047/
https://ncbi.nlm.nih.gov/pubmed/30367597
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12859-018-2425-6
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