Recently, I was doing an RNA-seq project, and I used spike-in control sequences in my experiment. So I mapped the reads to both human genome and spike-in sequences. And I successfully got the bam file, but when I tried to use the command samtools sort -o aa_sorted.bam aa.bam to sort the bam file according to the chromosome name, and got those confused order, here is the sorted bam file's header:
As you can see, The chromosomes marked with a red frame are placed in front of the chromosome 1. This result is really confusing. Can anyone help me here, thanks in advance.
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younglin113
samtools sort doesn't change the order of the chromosomes, it just sorts the alignments according to them. There are many tools that require that the order of the chromosomes match between fasta and BAM files, so if you start playing around with that order you're likely to run into problems. Note that you CAN do this, but you'll need to do something like:
# make a new header with the chromosomes in the order you'd like
# name it "header"
cat header <(samtools view original_sorting.bam) | samtools sort -o desired_sorting.bam -
Oh, so it is. Thanks a lot. So I just need to change the header and it can sort as I want it to, is that what you mean ?
Yes, but don't reheader the BAM file (this will completely screw things up), use something like I outlined where there's a SAM file produced and then piped into samtools sort.
Hello,
samtools sort sort the reads by position for each contig. It doesn't sort the contig itself, because this is usually not necessary.
The order of the contig names you see, is given by the order of the contigs in the reference file you specify during alignment.
fin swimmer
Thanks a lot. It's really helped my doubts.
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