hum0160 Release Note

Research IDRelease DateType of Data
hum0160.v2 2021/07/13 bam/gvcf data of NGS (WGS)
hum0160.v1 2019/05/28 NGS (WGS)

 

hum0160.v2

Whole genome sequencing analyzed data included in the JGAD000233 were mapped to the GRCh37 reference genome sequence, and variant detection was carried out using the GATK (Genome Analysis Toolkit) standards. Bam files and gvcf files were added. This project is an initiative of the GEnome Medical alliance Japan (GEM Japan, GEM-J).

 

hum0160.v1

DNAs extracted from cancer tissues and paired non-cancer (normal) tissues obtained from esophageal squamous cell carcinoma patients were used for WGS (HiSeq 2000/2500/X Five). Fastq files are provided (Paired-end).

 

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