Genomics Virtual Laboratory (GVL) Tutorials: Detecting small variants (SNVs and indels) using Galaxy workflow Input
收藏Research Data Australia2024-12-14 收录
下载链接：
https://researchdata.edu.au/genomics-virtual-laboratory-workflow-input/14049
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资源简介：
Short read data from the exome of chromosome 22 of a single human individual. There are one million 76bp reads in the dataset, produced on an Illumina GAIIx from exome-enriched DNA. This data was generated as part of the 1000 Genomes project: http://www.1000genomes.org/. Please use the ‘fastqsanger’ File Format
提供机构：
QFAB
