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6.3 years ago
siqizhao2018
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0
How to do peak correlation in m6A?Have Cancer and normal sample,but I have no idear to Make relevant with that。
How to do peak correlation in m6A?Have Cancer and normal sample,but I have no idear to Make relevant with that。
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Hi, do you have raw counts of every peak? The DESeq2 workflow may help you to correlate Cancer and normal sample(In section 4.3 Sample distances, http://master.bioconductor.org/packages/release/workflows/vignettes/rnaseqGene/inst/doc/rnaseqGene.html). Besides, you can also try to use corrplot package in R, but you may have to normlize your count data, and use log2(count+1) to tranform the data.
Hope this will help you. Aifu.
thank you! Yeah,In count I know how to do that,but I want to find some information in peak thinking~