I have a very large RNA-Seq sample size (n=100), so while performing quantification through featurecounts, Rstudio crashed. So, I decided to perform the analysis in chunks (n=20 bam files). Hence, I generated 5 lists through featurecounts (fc1,fc2....). Now I tried to merge all these lists in one list
fc, but the dimension of fc is list of 20 (ideally should have been- list of 4=> annotation;counts;target;stats).
Functions I used to merge lists-
c(fc1,fc2), mapply(fc1,fc2), rbind(fc1,fc2), Map(list,fc1,fc2).
What mistakes I might be doing? Any alternative for merging lists so that I get only one list (ideal list of 4)? Any other way so that I can process all files at once in R?