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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.
Kaydedildi:
| Yazar: | |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2010
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| Konular: | |
| Online Erişim: | 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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