基因组测序的点突变和小片段插入缺失的整合分析与解读 基因组测序的点突变和小片段插入缺失的整合分析与解读
Introduction
TNseq、TNScope和Varscan软件全基因组somatic突变数据分析推荐流程所构建的 系统的 APP。利用该 APP 可以获得从全基因组测序原始文件fastq
到包含somatic
突变信息的vcf
Publications
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Credits
- Ying Yu ying_yu@fudan.edu.cn Investigator
School of Life Sciences, Fudan University, China
Community Ratings
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Summary
Accession | BT007227 |
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Tool Type | Application |
Category | |
Platforms | |
Technologies | |
User Interface | |
Latest Release | v1.0 (July 11, 2021) |
Download Count | 806 |
Country/Region | China |
Submitted By | Ying Yu |
Fundings
2016YFC0901700