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Aligns tags from the same physical location against one another, calls SNPs from each alignment, and then outputs the SNP genotypes to a HapMap format file (one file per chromosome).
- To use gbsTagsToSNP_TASSEL 3.0.133, import your data in SAM and TBT format.
- Resources: Genotype-by-Sequencing
Use bwa_output.sam and myStudy.tbt.bin from the directory above as test input.
Parameters Used in App
When the app is run in the Discovery Environment, use the following parameters with the above input file(s) to get the output provided in the next section below.
- Default parameters only, no further configuration needed.
Expect a folder of text files as output. For the test case, the output folder you will find in the example_data directory is named unfilt.