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hg19K: addressing a significant lacuna in hg19‐based variant calling
BACKGROUND: The hg19 assembly of the human genome is the most heavily annotated and most commonly used reference to make variant calls for individual genomes. Based on the phase 3 report of the 1000 genomes project (1000G), it is now well known that many positions in the hg19 genome represent minor...
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| 發表在: | Mol Genet Genomic Med |
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| Main Authors: | , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
John Wiley and Sons Inc.
2016
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5241214/ https://ncbi.nlm.nih.gov/pubmed/28116326 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.251 |
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