載入...
FastGT: an alignment-free method for calling common SNVs directly from raw sequencing reads
We have developed a computational method that counts the frequencies of unique k-mers in FASTQ-formatted genome data and uses this information to infer the genotypes of known variants. FastGT can detect the variants in a 30x genome in less than 1 hour using ordinary low-cost server hardware. The ove...
Na minha lista:
| 發表在: | Sci Rep |
|---|---|
| Main Authors: | , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Nature Publishing Group UK
2017
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5451431/ https://ncbi.nlm.nih.gov/pubmed/28566690 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-02487-5 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|