Thanks.
my data set belong to human. I consruct bwa index(wg.fa) and for alignment I run below command:
bwa mem ~/cirRNA/apps/wg.fa sra_data_SRR1427482.fastq -t 30 > sra_data_SRR1427482_bwa.sam
and then in my terminal I have below result:
[M::bwa_idx_load_from_disk] read 0 ALT contigs
[M::process] read 8646532 sequences (300000008 bp)...
but after some minutes, my process will killed.
I also, ran this command for another sample and receive below message:
[M::bwa_idx_load_from_disk] read 0 ALT contigs
Segmentation fault (core dumped)
I appreciate if you share your comment with me.
Best Regards,
Mohammad
bwa is not an appropriate aligner for RNA-seq (unless it's prokaryotic), you should use a splice-aware aligner such as STAR or HISAT2.