Aligning short sequencing reads with Bowtie
- PMID: 21154709
- PMCID: PMC3010897
- DOI: 10.1002/0471250953.bi1107s32
Aligning short sequencing reads with Bowtie
Abstract
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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References
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Langmead B, Trapnell C, Pop M, Salzberg SL. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome. Genome Biol. 2009;10(3):R25. See above. Describes the indexing technique underlying the tool and compares to other alignment tools.
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