Closed arundurvasula closed 9 years ago
for i in `seq 1 12`; do samtools faidx ref.fa $i >> sorted_ref.fa; done
Then gzip your fasta and run
samtools faidx sorted_ref.fa.gz
to get your .fai file.
this was bc ref fastas weren't working if the chromosomes were out of order
Added to FAQ
Then gzip your fasta and run
to get your .fai file.