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Last seen 10.4 years ago
Hello,
I have three sequenced (Illumina) genomic libraries (L1,L2,L3) and
three biological replicates for each (A,B,C).
I'd like to compare those libraries, and find which are the most
similar (e.g. is "L1" more similar to "L2" or to "L3", based on the
profile of mapped short reads in the libraries).
I've generated windows of 2kb over the genome, and counted how many
reads from each library/replicate fall within the window.
The result is similar to this:
---
Window L1_RepA L1_RepB L1_RepC L2_RepA L2_RepB L2_RepC L3_RepA
L3_RepB L3_RepC
chr1_1 10 15 0 1000 1100 800 90
0 300
chr1_2 77 80 99 3 4 12 100
200 193
...
(and so forth for every window over the chromosomes).
---
What would be a reliable way to compare these three libraries, as a
whole (meaning, not just "differential expression" on each window
independently, as would be done with genes) ?
Thank you,
-gordon
-- output of sessionInfo():
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