A quality control analysis tool for high throughput sequencing data
Open Source Monitoring System for performance and availability.
script for variant calling of RNA-Seq
convert genome coordinates betweeen assemblies
An intuitive and efficient tool for preprocessing Illumina FASTQ reads
script for variant calling of Exome-Seq
A de novo local assembler for paired reads
RNASeqBrowser: A genome browser for strand specific RNAseq reads
Reanalysis of somatic APP retrotransposition
shell script to run SVDetect with baseline adjustment
hiddenDomains: a modern HMM to identify ChIP-seq enrichment
miRPlant: An Integrated Tool for Identification of Plant miRNA
MiRDeep*
script of SV calling in Exome-seq
ChIP-seq coverage island analysis algorithm for broad histone marks
Pure java NGS mapping soft run on Hadoop 2.0
A tool to detect mid sized tandem duplications
Use Apache Pig to process your large sequencing datasets!
MIP VARiant calling tool
Reference based genome assembly and annotation for new genome
Non-Coding RNA PROfiling from sRNA-seq