Hello,
it's a really impressive method. And I want to use this method in my project. But I have multical 10X single cell samples, and I ran one by one following your 'Instructions for Manual Implementation of Our Pipeline'. I got multical Peaks.rds files but I was stucked in merging them. Could you show me how could I merge mutical samples' peaks.rds files or merge multical objects in R and how to extract only some cells I was interested in the 'peak' object.
Thanks and Merry Christmas!
Hello,
it's a really impressive method. And I want to use this method in my project. But I have multical 10X single cell samples, and I ran one by one following your 'Instructions for Manual Implementation of Our Pipeline'. I got multical Peaks.rds files but I was stucked in merging them. Could you show me how could I merge mutical samples' peaks.rds files or merge multical objects in R and how to extract only some cells I was interested in the 'peak' object.
Thanks and Merry Christmas!