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A cross-sample statistical model for SNP detection in short-read sequencing data
Highly multiplex DNA sequencers have greatly expanded our ability to survey human genomes for previously unknown single nucleotide polymorphisms (SNPs). However, sequencing and mapping errors, though rare, contribute substantially to the number of false discoveries in current SNP callers. We demonst...
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| Autors principals: | , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2012
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3245949/ https://ncbi.nlm.nih.gov/pubmed/22064853 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkr851 |
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