Genomics
Pre-configured workflows for DNA, RNA, and sequencing data analysis
Tools and workflows for analyzing DNA, RNA, and other sequencing data — from quality control to variant calling.
This category covers:
- Quality control — assess and validate sequencing data quality
- Genome assembly — de novo assembly and scaffolding
- RNA-Seq analysis — transcriptome quantification and differential expression
- Variant calling — SNP and indel detection
- Genome annotation — functional annotation and analysis
Browse the workflows below. To deploy one, see How it works.