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vi-HMM: a novel HMM-based method for sequence variant identification in short-read data
Abstract Background Accurate and reliable identification of sequence variants, including single nucleotide polymorphisms (SNPs) and insertion-deletion polymorphisms (INDELs), plays a fundamental role in next-generation sequencing (NGS) applications. Existing methods for calling these variants often...
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Asıl Yazarlar: | , , , , |
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Materyal Türü: | Artigo |
Dil: | Inglês |
Baskı/Yayın Bilgisi: |
BMC
2019-02-01
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Seri Bilgileri: | Human Genomics |
Konular: | |
Online Erişim: | http://link.springer.com/article/10.1186/s40246-019-0194-6 |
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