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I'm trying to understand how to run the cite-seq-count with data made with the 10x protocol for Next GEM Single Cell 3' HT v3.1.
Reading the user manual for the tool, I should run the command with -R1, which containing the barcodes/UMIs and with -R2, which contain the antibody barcodes.
When I download the fastq files of the 10x protocol from here and untar them, I get two separate output folders, both folders are in paired-end mode, as is the usual for 10x data. One folder contains I1, R1 and R2 for two lanes for the RNA data, the second folders contains also I1, R1 and R2 but for the antibody results.
Hi @yeroslaviz , have you solved the problem?
I've just download the same files and feel very puzzled about the cite-seq-count command.
Any suggestions would be appreciated!
I'm trying to understand how to run the
cite-seq-count
with data made with the 10x protocol for Next GEM Single Cell 3' HT v3.1.Reading the user manual for the tool, I should run the command with
-R1
, which containing the barcodes/UMIs and with-R2
, which contain the antibody barcodes.When I download the fastq files of the 10x protocol from here and untar them, I get two separate output folders, both folders are in paired-end mode, as is the usual for 10x data. One folder contains I1, R1 and R2 for two lanes for the RNA data, the second folders contains also I1, R1 and R2 but for the antibody results.
Can you please explain to me, how I use these files with the
cite-seq-count
command?Do I use only the
R2.fastq
files as input?thanks
Assa
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