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Toward better understanding of artifacts in variant calling from high-coverage samples
Motivation: Whole-genome high-coverage sequencing has been widely used for personal and cancer genomics as well as in various research areas. However, in the lack of an unbiased whole-genome truth set, the global error rate of variant calls and the leading causal artifacts still remain unclear even...
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| Vydáno v: | Bioinformatics |
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| Hlavní autor: | |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Oxford University Press
2014
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4271055/ https://ncbi.nlm.nih.gov/pubmed/24974202 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btu356 |
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