Hi all,
Just wondering about a good method to see bigWigs normalized to one another in the genome browser, based on read count? Have used deepTools to compare and get fold change and have done scaling factors, but basically need to see two bigwigs side by side that have been normalized according to read count. Thanks!
LH
Just wondering about a good method to see bigWigs normalized to one another in the genome browser, based on read count? Have used deepTools to compare and get fold change and have done scaling factors, but basically need to see two bigwigs side by side that have been normalized according to read count. Thanks!
LH
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