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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Bibliografiset tiedot
Julkaisussa:BMC Bioinformatics
Päätekijät: 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
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2018
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Linkit: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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