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Hi,
I used the Sabre to demultiplex data but no matter if I add -c parameter or not, the output demultiplexed fastq files are only 0 reads.
The first column is the size of the file which are all 0.
But the unmached R1 amd R2 fastq files seem large:
Does this mean there is something wrong with my barcode mapping file, or can be some parameter issues that I have not addressed yet?
Thanks! Leran
The text was updated successfully, but these errors were encountered:
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Hi,
I used the Sabre to demultiplex data but no matter if I add -c parameter or not, the output demultiplexed fastq files are only 0 reads.
The first column is the size of the file which are all 0.
But the unmached R1 amd R2 fastq files seem large:
Does this mean there is something wrong with my barcode mapping file, or can be some parameter issues that I have not addressed yet?
Thanks!
Leran
The text was updated successfully, but these errors were encountered: