Dear All
Could you suggest how I can use paired-end GBS data for GWAS analysis using Tassel?
Tassel-GBS v2 pipeline gives vcf / hmp output for each read (forward/reverse). SNP output (genotypic file) has data for samples as Amber_1 and Amber_2, whereas I have phenotypic data for sample names, such as Amber.
Could you suggest how I can make use of paired-end SNP output (hmp.txt) for GWAS analysis using Tassel?
Could you also suggest alternatives (softwares/tools/methodology) to solve this problem?
Thanks and regards
Suran