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Variant calling on the GRCh38 assembly with the data from phase three of the 1000 Genomes Project
We present a set of biallelic SNVs and INDELs, from 2,548 samples spanning 26 populations from the 1000 Genomes Project, called de novo on GRCh38. We believe this will be a useful reference resource for those using GRCh38. It represents an improvement over the “lift-overs” of the 1000 Genomes Projec...
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| 出版年: | Wellcome Open Res |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
F1000 Research Limited
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7059836/ https://ncbi.nlm.nih.gov/pubmed/32175479 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/wellcomeopenres.15126.2 |
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