Hello Irene,
The file is described in the TopHat manual:
http://tophat.cbcb.umd.edu/manual.html#output
Along with the insertion files, deletions describes variation between
the query and the reference genome at the base level (nucleotide). It
does not describe whole transcripts or genes.
How
dear all,
how can we use the tophat deletions output?
e.g. if I want to see and conpare between two samples if a specific
gene or transcript had been deleted, how can I use this output?
is visualisation enough?
thanks,
ib
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