That probably means all the data in your in.bam is flagged READ1 or READ2, so 
you need to specify the -1 and -2 options.


> On 1 Feb 2016, at 10:00, Robert May <[email protected]> wrote:
> 
> 
> fastq/a
> samtools fastq [options] in.bam 
> samtools fasta [options] in.bam
> Converts a BAM or CRAM into either FASTQ or FASTA format depending on the 
> command invoked.
> 
> using this command (0=zero fasta=.fa or.fai)
> 
> samtools fasta -n -0 out .fai in.fasta
> 
> the result I get if that the .fa or .fai file is created with o KB but the 
> fasta is printed to the screen.
> 
> I cant see any other options
> any ideas
> 
>  Bob May
> DNA Projects I2b L415, I2c L596 HG, Spriggs of Cleve SA Family & Tyler 
> Surname and ISOGG YTree 
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