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Hi, is there a way to get the command line processing of SMARTseq2 BAM files to use ensembl IDs from the gtf file instead of a mixture of HGNC and other gene names so that I won't have inconsistencies of gene name versioning between multiple analysis packages?
Thank you
The text was updated successfully, but these errors were encountered:
Hi, is there a way to get the command line processing of SMARTseq2 BAM files to use ensembl IDs from the gtf file instead of a mixture of HGNC and other gene names so that I won't have inconsistencies of gene name versioning between multiple analysis packages?
Thank you
The text was updated successfully, but these errors were encountered: