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FermiKit: assembly-based variant calling for Illumina resequencing data
Summary: FermiKit is a variant calling pipeline for Illumina whole-genome germline data. It de novo assembles short reads and then maps the assembly against a reference genome to call SNPs, short insertions/deletions and structural variations. FermiKit takes about one day to assemble 30-fold human w...
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| 出版年: | Bioinformatics |
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| 第一著者: | |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2015
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4757955/ https://ncbi.nlm.nih.gov/pubmed/26220959 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btv440 |
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