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3 hours ago by

My honours thesis project aims to find genetic variation (or lack of) between termite populations (one invasive, one native, and one intermediate). I have 9 transcriptome termite libraries (3 locations x 3 castes), but do not have a reference assembly. I have tried to map the libraries to a closely related species, and also to Drosophila using BaseSpace Illumina RNA-Seq Alignment. The RNA-Seq Analyses I have tried to run eventually get aborted ~5 hours in (my fastq files are properly formatted, and everything is named correctly). I am wondering if you can please help me understand the issue I might be having with the RNA-Seq App or if you have any suggestions on how I can accomplish my overall goal without mapping the libraries to a reference (i.e. is there a way to map them to each other).


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