Closed berixD closed 4 years ago
Hi, I think the easiest thing for you to do might be to call peaks on each group of cells and then quantify reads in those peaks using the FeatureMatrix
function. You can write the cell names for each group to a file and then split the bam file by into different file for each group of cells using sinto, and then call peaks using the split bam files.
I don't have a command list for the package available right now, but I will add this to my list of things to do for Signac.
Thanks for the quick reply! I will try the FeatureMatrix option:)
Hi timoast, Signac is a great tool. Thanks for that! I would like to extract the normalized accessibility data for all identities as plotted with CoveragePlot. With this data, I would like to know all regions of open chromatin (above a certain threshold) in order to look for cis-acting elements. I tried looking at the functions buildup and came up with the idea to use the cutmat matrix. But I am stuck, because I dont know how to do it for all identities and multiple regions in an efficient way.
Thanks in advance!
Ps. Is a command list of the signac package avialable? Something similar to Seurat's one would be nice https://satijalab.org/seurat/essential_commands.html