CRISP 0.2 – Detection of SNVs and Short Insertion/deletion variants from Pooled high throughput DNA sequencing data

CRISP 0.2

:: DESCRIPTION

CRISP (Comprehensive Read analysis for Identification of Single Nucleotide Polymorphisms from Pooled sequencing) is a software program to detect SNPs and short indels from pooled sequencing data generated using next-generation sequencing instruments. CRISP is designed to detect both rare and common variants by utilizing sequence reads from next-generation sequencing of multiple DNA pools.

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::DEVELOPER

Bansal Lab

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  •  Linux

:: DOWNLOAD

 CRISP 

:: MORE INFORMATION

Citation

Bioinformatics. 2010 Jun 15;26(12):i318-24. doi: 10.1093/bioinformatics/btq214.
A statistical method for the detection of variants from next-generation resequencing of DNA pools.
Bansal V.