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A new tool for prioritization of sequence variants from whole exome sequencing data
BACKGROUND: Whole exome sequencing (WES) has provided a means for researchers to gain access to a highly enriched subset of the human genome in which to search for variants that are likely to be pathogenic and possibly provide important insights into disease mechanisms. In developing countries, bioi...
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| 出版年: | Source Code Biol Med |
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| 主要な著者: | , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
BioMed Central
2016
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4929716/ https://ncbi.nlm.nih.gov/pubmed/27375772 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13029-016-0056-8 |
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