I recently sorted a bunch of BAMs that are about 400 MB in size each. After sorting with samtools the output sorted BAMs are about 3-4 MB smaller than the unsorted originals. Does anyone know why this is? My understanding of a sort is that it simply rearranges the available reads inside a BAM, and I don't see why this would create a smaller file.
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Is there any chance that the unsorted BAM included unmapped reads and the sorted one doesn't? What did you use for alignment?
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Sorting does not remove duplicate reads.
I seem to recall this same question asked previously on Seqanswers but my search skills are lacking this morning so I can't find the thread. If you were to compare an unsorted vs. sorted SAM file the sizes should be identical because, as oiiio said, the information content is the same, it has simply been rearranged. SAM files are plain text files so provided the content is the same the file size will be the same regardless of order. BAM files are compressed; the order of the information in the file can have an effect on the compression of that data. This was the explanation I recall from that earlier thread. (Once the caffeine fully kicks in I'll see if I can find that thread.)
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I know this thread has been inactive for a while, but my question is basically the same.
I have a 120GB bam file from RNA-Seq data and used the samtools sort function with compression level 1 (so meaning the least compression).
I ended up with a file of only ~30GB size.
Now this is the first time I am working with this and I have no idea if this is a normal range for reduction in size, but my feeling is something went wrong.
Could anyone with experience tell me if the result is expected or not?
thanks,
Florian
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RNA-Seq contains a greater fraction of duplicate reads due to highly expressed genes, so sorting reduces the size more than DNA-Seq. If you want to check that nothing was lost, use 'samtools view' to compare the number of reads before/after sorting.
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Using 'samtools index' and then 'samtools idxstats' on a sorted file will give you total counts for mapped and unmapped reads, which is slightly easier to check compared to looking at a few million lines to find what's missing.Originally posted by HESmith View PostIf you want to check that nothing was lost, use 'samtools view' to compare the number of reads before/after sorting.
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