Entering edit mode
5.2 years ago
Zee_S
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60
Dear Biostars commmunity,
I am seeking your advice to know if there is a way to overlap chip-seq scores distributed across 0-based consecutive genomic bins (generated by Deep tools multiBigwigSummary) onto expression scores generated for RNA-seq data distributed in similar consecutive genomic bins, which are instead 1-based coordinates (generated from HTseq)? Are they already comparable as they are?
illustration of my question:
multiBigwigSummary chip-seq scores in 0-based genomic bins:
chr1 0 10000 0.9402239918708801 "bin 1;"
chr1 10000 20000 0.7390850186347961 "bin 2;"
chr1 20000 30000 0.35219499468803406 "bin 3;"
HTseq rna-seq scores in 1-based genomic bins:
chr1 1 10000 0.5 "bin 1;"
chr1 10001 20000 1.2 "bin 2;"
chr1 20001 30000 1.8 "bin 3;"
Thanks a lot for your help!
Why not just to modify your multiBigwig file to be 1-based? You already compute the bins, coordinates representation is just where the range is located.
hi JC, thanks a lot for your answer. How exactly do i do that? i was thinking that if i modify the multi bigwig coordinates to 1-based, the score in column 4 that was calculated for the original 0-based coordinate will no longer be valid (since now the 1-based causes the bin to shift by 1 base pair?). or am i wrong?
Coordinates are just representation of the positions, for example:
The coordinates can be represented as:
understood. thank you so much for your help!