*** Per base coverage ***

[Michael.James.Clark]

Alternatively:

samtools view -b <in.bam> <chr>:<pos>-<pos> | samtools pileup - | grep <pos> | awk '{print $4}'

[cristae8]

Thanks, everyone. bedTools seems to work the best and it's fully documented so very easy to use! Much thanks to Aaron (the author) & Pete.

[tanmoy63]

you can use samtools pileup -c from on sorted indexed bam file of your alignment..this pileup consensus will give you read depth in each position and base composition in each also

[PeteH]

The coverageBed function in bedtools (http://code.google.com/p/bedtools/) should be able to do what you want.

[kwatts59]

I loaded all my short read data into an SQL database so that this information can be pulled out with a quick query.

For example, to find how many reads cover position 72342 of chr 1, just type in the following query. This assumes 50bp reads.

select count(*) from short_reads
where (chromosome = 'chr1')
and (start_position >= 72293)
and (start_position <= 72342)

To perform this query for many SNPs, a PERL script can be written.

[cristae8]

Hi,
This seems like a silly question, but I can't quite find the answer for it anywhere. I have a list of single nucleotide position, ie,
chr 1 72342
chr 2 32912
chr X 184343
etc,
to which I would like to find their coverage, ie, how many reads cover that position and what are those bases.
This is almost like calling SNP, but not quite because I just like to know the coverage even if no SNP is present. For this reason, I can't just use a SNP caller. Does anyone have a solution for this?
Thanks so much.