Software
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The following is a categorized list of software available through the GSAF. Each page lists a summary of the software, the hardware it is currently installed on, links to user documentation, and helpful tips.
Contents
References (by organism)
General purpose tools
Microarray data analysis tools
Mappers/Aligners
- mapreads SOLiD data only, ungapped alignment
- MAQ - best for short-read SNP calling; ungapped alignment
- SOAP - very fast and versatile: any read length, gapped, paired-end, SNP calling
- SSAHA & SSAHA2 - like Maq, fast for ungapped mapping - SNP calling, contig placement to reference, etc.
- Bowtie - very fast, ungapped alignment. Does not support color space data
- SHRiMP - A sensitive and accurate mapper. Supports color space data and gapped alignment.
- BFAST - BLAT-like short read mapper. Natively supports SOLiD colorspace short reads.
- BWA - The successor to MAQ; a BW mapper, but which allows for gaps and handles colorspace natively.
- See Category:Mapper for more details.
Gene prediction tools
SNP discovery
- Corona-Lite - SOLiD data only
- MAQ - best for short-read SNP calling; ungapped alignment
- SOAP - very versatile: any read length, gapped, paired-end, SNP calling
- SAMTOOLS
Splice Junction discovery
Genome Alignment and Visualization
- MaqView
- Mauve
- Affymetrix Integrated Genome Browser: easy to install genome browser. Download here
De novo genome assembly
454 Analysis tools
Useful scripts
Software users group meetings
- Small-rna data analysis - Lessons learned during Sullivan data analysis
- Mapping of short reads - Comparison of few publicly available mapping tools