Hi,
I am trying to run the allelotype lobSTR_4.0.6 on a hg38 bam file generated with BWA_MEM.
I used the command suggested in the documentation:
allelotype \
--command classify \
--bam my_sample_output.sorted.bam \
--index-prefix hg19_v3.0.2/lobstr_v3.0.2_hg19_ref/lobSTR_ \
--strinfo hg19_v3.0.2/lobstr_v3.0.2_hg19_strinfo.tab \
--noise_model models/illumina_v3.pcrfree \
--out my_sample_output
The bam file was aligned earlier using BWA-MEM. The index and strinfo were built by me using data downloaded from the Tandem Repeat Database. The noise_model was the same as the example.
I received the error message "ERROR: No read groups found".
I also try to add the --realign flag but nothing change. I am wondering if someone knows what happens? Thanks in advance.