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Hello, I need to merge two fastq files, which belong to two flowcell, one file has 71 ind and the other 96, so in total they are 167 ind. How can I merge them? I'm analyzing the cyverse data with...
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I want to use Boruta and VSURF with my SNPs and phenotype data, but I don't know how to set up the input and run it in R. Can anyone help me? Thanks! Mariana
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