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Genotype and SNP calling from next-generation sequencing data | |
Rasmus Nielsen; Joshua S. Paul; Anders Albrechtsen; Yun S. Song | |
2011 | |
Source Publication | Nature Reviews Genetics
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Volume | 12Issue:xPages:443-451 |
Abstract | Meaningful analysis of next-generation sequencing (NGS) data, which are produced extensively by genetics and genomics studies, relies crucially on the accurate calling of SNPs and genotypes. Recently developed statistical methods both improve and quantify the considerable uncertainty associated with genotype calling, and will especially benefit the growing number of studies using low- to medium-coverage data. We review these methods and provide a guide for their use in NGS studies. |
Document Type | 期刊论文 |
Identifier | https://ir.xtbg.ac.cn/handle/353005/4694 |
Collection | 文献共享 |
Recommended Citation GB/T 7714 | Rasmus Nielsen,Joshua S. Paul,Anders Albrechtsen,et al. Genotype and SNP calling from next-generation sequencing data[J]. Nature Reviews Genetics,2011,12(x):443-451. |
APA | Rasmus Nielsen,Joshua S. Paul,Anders Albrechtsen,&Yun S. Song.(2011).Genotype and SNP calling from next-generation sequencing data.Nature Reviews Genetics,12(x),443-451. |
MLA | Rasmus Nielsen,et al."Genotype and SNP calling from next-generation sequencing data".Nature Reviews Genetics 12.x(2011):443-451. |
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Genotype and SNP cal(1407KB) | 开放获取 | CC BY-NC-SA | View Download |
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