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Stampy is a package for the mapping of next gen sequencing reads onto a reference genome. Stampy excels in the mapping of reads containing sequence variation relative to the reference, especially indels.
- To use Stampy-build-and-map, import your data in fastq format.
Use the test_1.fastq file from the directory above as test input with the genome sequence provided, NC_010473.fa.
Parameters Used in App
- Default parameters only, except set the output file name to stampyout.sam
Expect a SAM file named stampyout.sam as output in the test case.