Closed rcavalcante closed 8 years ago
Grab chr21
from the .bam
s and convert to .fastq
to use as the starting point.
Have chr21
test data for hybrid_compare, hybrid_sample, pulldown_compare, and pulldown_sample. Runtimes are reasonably fast for the pulldown. Could improve for hybrid.
I think I'll look for regions of PePr peaks, and collect those regions so we're still getting some interesting signal to look at for testing.
The part that takes the longest is the cytosine report in bismark. If only we didn't need that...
mint
needs small test data to run the pipeline variants from end to end. It is becoming cumbersome to test on theGSE52945
andGSE63743
when pipeline changes are made. The problem with small test data is that there isn't a lot to work with because the reduced number of reads don't translate to methylation rates or peaks, and consequently differential methylation and classifications.