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xGAP: a python based efficient, modular, extensible and fault tolerant genomic analysis pipeline for variant discovery
MOTIVATION: Since the first human genome was sequenced in 2001, there has been a rapid growth in the number of bioinformatic methods to process and analyze next-generation sequencing (NGS) data for research and clinical studies that aim to identify genetic variants influencing diseases and traits. T...
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| 出版年: | Bioinformatics |
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| 主要な著者: | , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2021
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8034531/ https://ncbi.nlm.nih.gov/pubmed/33416856 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btaa1097 |
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