Open tequilasunrise0 opened 7 months ago
Thanks for developing the tool!
I have Smart Seq 2 data. I've tried either fastq files or bam file as input, but it always give me such result:
[alignment] Processed 29558126 reads, 0 pseudoaligned to HLA reference [alignment] 0 reads mapped to a single HLA gene
Many valid reads, but 0 mapped to HLA. How can I solve this?
Very appreciate!
Thanks for developing the tool!
I have Smart Seq 2 data. I've tried either fastq files or bam file as input, but it always give me such result:
[alignment] Processed 29558126 reads, 0 pseudoaligned to HLA reference [alignment] 0 reads mapped to a single HLA gene
Many valid reads, but 0 mapped to HLA. How can I solve this?
Very appreciate!