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Aligning short sequencing reads with Bowtie

This unit shows how to use the Bowtie package to align short sequencing reads, such as those output by second-generation sequencing instruments. It also includes protocols for building a genome index and calling consensus sequences from Bowtie alignments using SAMtools.

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Detalhes bibliográficos
Autor principal: Langmead, Ben
Formato: Artigo
Idioma:Inglês
Publicado em: 2010
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3010897/
https://ncbi.nlm.nih.gov/pubmed/21154709
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/0471250953.bi1107s32
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