Hi everyone,
I aligned my reads using tophat and loaded the results in R to do the DE analysis using DESeq. I feed it an exon annotation and get...
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DE exons to DE transcripts
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Table of transcript variant 1
Hi all,
I really hope that someone could help me.
I would like to have a table that reports the information about the all the transcripts...
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Looking for no-hits within Sample & Reference Genome
Hi pals,
This is amarth, and my question is:
How can I extract no-hits data from the alignment of the sample, with the...