Before including it in our analysis pipeline, I wanted to give it a quick check, and set up this:
— we have a small sample processed with cellranger 3.1
— run bamtofastq on this sample possorted.bam
— run cellranger on bamtofastq output
— compare original and restored matrices.
Unfortunately, they are not identical. In the filtered_feature_bc_matrix I see a small difference in barcodes.tsv.gz for example. I wonder, what is causing this and how to debug it?
Sorry for disturbance, I found out that I used different reference genome for the second run. When I used the same reference genome as for the original run, the results were identical. Thank you
Thank you for the tool.
Before including it in our analysis pipeline, I wanted to give it a quick check, and set up this:
— we have a small sample processed with cellranger 3.1 — run bamtofastq on this sample possorted.bam — run cellranger on bamtofastq output — compare original and restored matrices.
Unfortunately, they are not identical. In the
filtered_feature_bc_matrix
I see a small difference in barcodes.tsv.gz for example. I wonder, what is causing this and how to debug it?