A fast and sensitive gapped read aligner
The UEA sRNA Workbench
A Fast, OpenSource Program for Docking Ligands to Proteins and N.Acids
A desktop application for analyzing whole genome VCF files
flexible barcode and adapter removal for sequencing platforms
Quality control and filtration for illumina sequencing data
Parallel Processing for Next-Generation Sequencing (NGS) Analysis
A hypocotyl phenotyping software
Novel sequence insertion detection