Hi,
I have a bigWig file containing single-cell RNA-seq data of ~50k individual cells (public dataset obtained from GEO). I would like to run some tests analyzing the profiles of individual cells. However, I don't seem to be able to retrieve individual cells from the bigWig file but, instead, I obtain a bedGraph/coverage track of all cells combined (I used UCSCtools bigWigToWig + bedops wig2bed).
Is it really possible to obtain individual cells from the bigWig file or I will only get a pool of all samples?
Thanks,
Txema
Oh, dang!
It seems that the raw BAMs are not available, but I could find what seems to be the count matrix.
This file has 3 columns. From what I understand, the first column is the gene_ID, the second column is the cell_ID, and the third column is the ¿count? ¿count of reads overlapping the gene? ¿partially of fully covering the gene?
I am interested in analyzing partial/complete or blocked transcription. Can I work with this count matrix or I would need the raw data to do it?
Thanks,
Txema
I would personally always start from raw data unless there is processed data and a crystal-clear explanation how these data have been processed computationally. With raw data I mean fastq files.