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While extracting bam files from SRA, there might be a problem if you use the standard commands from samtools.
For example, in this dataset, if you run:
While extracting bam files from SRA, there might be a problem if you use the standard commands from samtools.
For example, in this dataset, if you run:
It will not get the original 10xBAM file with required headers for Cell Ranger to perform the alignment.
This is also mentioned here:
'Invalid BAM record: read: "1" is missing tag: "CR"'
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