Sounds like you're using the wrong reference file for that bam?
Looking at the header of bam, it's clearly been aligned with a non-standard 
reference fasta.


> On 17 May 2015, at 10:12, Dan Greenfield <d...@storleap.com> wrote:
> 
> Dear all,
> 
>    I encountered a problem converting a BAM file to CRAM and back again. This 
> problem is exhibited on both samtools 1.1 and the latest download for 
> samtools 1.2, each time reproduced from the first step.
> 
> Steps to reproduce this:
> 1. download original BAM from EBI: 
> ftp://ftp.sra.ebi.ac.uk/vol1/ERA172/ERA172924/bam/NA12878_S1.bam
> 2. convert to CRAM:
>     samtools view -C -o NA12878_S1.cram -T hg38.fa NA12878_S1.bam     
> 3. attempt to convert back to BAM:
>     samtools view  -b -o NA12878_S1.cram.bam -T hg38.fa NA12878_S1.cram
> 
> Results from step 3: (no errors/warnings encountered in previous steps)
> 
> Slice ends beyond reference end.
> Slice ends beyond reference end.
> ERROR: md5sum reference mismatch for ref 1 pos 248900092..248956422
> CRAM: 1ca5fd5ffe82936260309c85fc9b473b
> Ref : b47b43c987dbf1af96ca6d59061401c8
> Failure to decode slice
> [E::hts_close] Failed to decode sequence.
> samtools: error closing "NA12878_S1.cram": -1
> 
> Here are the file sizes (note the cram file is actually bigger than the 
> original bam):
> NA12878_S1.bam 121,691,186,161
> NA12878_S1.cram 125,386,599,695
> NA12878_S1.cram.bam 11,109,478,067
> 
> Regards,
>    Dan
> 
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