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

是根据 Sentieon 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 Choppy-pipe 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文件的整个过程。主要包括数据的预处理、中间数据质控以及变异的检测。

Publications

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Credits

  1. Ying Yu ying_yu@fudan.edu.cn
    Investigator

    School of Life Sciences, Fudan University, China

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Summary
AccessionBT007227
Tool TypeApplication
Category
Platforms
Technologies
User Interface
Latest Releasev1.0 (July 11, 2021)
Download Count806
Country/RegionChina
Submitted ByYing Yu
Fundings

2016YFC0901700