Hi Sung-Huan,

At least on my laptop I can't reproduce this (I get the expected bcf file 
output), though since I don't have your fasta file perhaps that's why. Could 
you post that somewhere as well?

Best,
Devon

____________________________________________
Devon Ryan, Ph.D.
Email: [email protected]
Tel: +49 (0)178 298-6067
Molecular and Cellular Cognition Lab
German Centre for Neurodegenerative Diseases (DZNE)
Ludwig-Erhard-Allee 2
53175 Bonn, Germany

On Sep 19, 2014, at 2:19 PM, Sung-Huan Yu wrote:

> Dear all,
> 
> I would like to use samtools to call SNP. I use the latest version 1.0.
> First, I have to generate bcf file.
> I run the following command.
> 
> samtools mpileup -t DP -ugf my.fasta my.bam
> 
> the result is always like this:
> 
> [mpileup] 1 samples in 1 input files
> Set max per-file depth to 8000
> Aborted
> 
> If I just run
> 
> samtools mpileup -f my.fasta my.bam
> 
> it works fine.
> I have no idea what happens.
> If I go back to use samtools-0.1.19 to run
> 
> samtools mpileup -uD -f my.fasta my.bam
> 
> everything is okay.
> Could anyone helps me? Thank you.
> 
> I also parsed the BAM file to short one. I found when the line comes to 88, 
> it will aborted. Before line 88, everythin is fine. But I checked the file, I 
> didn't see anything wrong. Please refer the attachment.
> Sung-Huan
> 
> 
> <short.bam>------------------------------------------------------------------------------
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