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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Xehetasun bibliografikoak
Argitaratua izan da:BMC Bioinformatics
Egile Nagusiak: 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
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2018
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Software
Sarrera elektronikoa: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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