Rainbow is a scalable workflow for whole genome sequencing analysis. It combines:
- PICARD, a Java-based command-line utility that manipulates SAM/BAM files
- Bowtie, an ultrafast and memory efficient short read aligner
- SoapSNP, an accurate genotyper
- SNP_Merger, an in-house developed application for SNP consolidations
These tools are combined in Semi-automatic, parallel pipeline that runs in the cloud (Amazon Web Services’ EC2, S3, and Elastic MapReduce offerings in this case).
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