dragen学习资料汇总

文档

• dragen在线帮助文档
• dragen软件下载
• dragen-bio-it-platform-Getting Started Guide.pdf
• dragen-platform-v4.2-guide.pdf
• 4.2-Customer-Release-Notes.pdf

流程使用说明

• 数据拆分
• 遗传病WGS
• 遗传病WES
• 数据压缩
• RPIP
• 参考基因组
• 测序系统误差
• 体细胞-tumor-only
• 体细胞-tumor vs normal
• 变异注释
• RNAseq数据分析
• 第三方工具兼容

Explore recent

DRAGEN publications

Illumina DRAGEN Bio-IT Platform Product Files

Behera S, Catreux S, Rossi M, et al. Comprehensive and accurate genome analysis at scale using DRAGEN accelerated algorithms[J]. bioRxiv, 2024: 2024.01. 02.573821.

Scheffler K, Catreux S, O’Connell T, et al. Somatic small-variant calling methods in Illumina DRAGEN™ Secondary Analysis[J]. bioRxiv, 2023: 2023.03. 23.534011.

Resource

a population SNP VCF， can be used --cnv-population-b-allele-vcf option

1000G_phase1.snps.high_confidence.b37.vcf.gz

1000G_phase1.snps.high_confidence.hg38.vcf.gz

Technical Assistance

Email: techsupport@illumina.com

Illumina Technical Support Telephone Numbers

Region	Toll Free	International
china		+86 400 066 5835