Question: How to use "Mpileup" for getting information of the reads of the SNP from the BAM files?
gravatar for jigarnt
16 months ago by
jigarnt30 wrote:

Hi All,

I am thinking of using Mpileup from Samtools to get the information on the read quality and read depth from the BAM files. In that case which script should I use?

I have been recommended the script below:

ref=my_fasta.fasta samtools mpileup -f $ref -r chromosome_1:1018000-1018100 my_bam.bam my_bam2.bam

P.S. I dont have to do Variant calling, just need the read information.

Thanks in advance for your help.

mpileup snp bam genome • 569 views
ADD COMMENTlink modified 16 months ago by agata88630 • written 16 months ago by jigarnt30
gravatar for agata88
16 months ago by
agata88630 wrote:

I would not use mpileup at all - if you need only alignment statistics. Use BedTools. For example here : A: How to get coverage for an alignment file The read quality you can get from FASTQC

But to be clear:

First what you should do is to check your reads by FASTQC (if the quality is bad do trimming), then align them to reference and then perform BedTools.



ADD COMMENTlink written 16 months ago by agata88630
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