Hi pals,
This is amarth, and my question is:
How can I extract no-hits data from the alignment of the sample, with the reference genome?
My main goal is not to visualize differential expression of genes (maybe it is, as a partial goal), but the main one, is to identify genes (maybe from a virus) expressed in all the transcript RNA of a sample with symptoms of the disease, but not in a healthy sample.
This is amarth, and my question is:
How can I extract no-hits data from the alignment of the sample, with the reference genome?
My main goal is not to visualize differential expression of genes (maybe it is, as a partial goal), but the main one, is to identify genes (maybe from a virus) expressed in all the transcript RNA of a sample with symptoms of the disease, but not in a healthy sample.
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