count reads with samtools view
2
0
Entering edit mode
9.2 years ago
schelarina ▴ 50

Hello,

I want to count reads starting at a specific position e.g position 10000 in chromosome 1, output 50 reads start at position 10000

Here is the command that I run and gave me the correct output that I need:

samtools view -F 16 file.bam | grep chromosome_1 | awk '{print $4}' | grep -w 10000 | wc -l

I have a list of positions in a file.txt and for every position I would like to count how many reads start at that position and save the output in new file in this way: position 10000 counts 50

How can I do this in automatic way without entering the command for each position?

Thanks!

RNA-Seq next-gen sequence alignment • 3.4k views
ADD COMMENT
0
Entering edit mode
9.2 years ago
tiago211287 ★ 1.5k

you can use in your txt, assuming there is one number per line:

   samtools view -F 16 file.bam | grep chromosome_1 | awk '{print $4}' > positions.txt
   sort positions.txt | uniq -c > output.txt

Then you can use grep again to look for some specific position.

grep 1000 output.txt
ADD COMMENT
0
Entering edit mode
9.2 years ago
put your positions in a bed file, use the BAM index and use awk to count the lines.
sed -e 's/\t/:/' -e 's/\t/-/' input.bed |\
read F
do
   samtools view -F 4 - "${F}" |\
    awk -v "p=$F" 'BEGIN{n=0;split(p,a,/\-/);} {if($4==a[2]) n++;} END{ printf("%s\t%d\n",p,n);}'
done
ADD COMMENT

Login before adding your answer.

Traffic: 1654 users visited in the last hour
Help About
FAQ
Access RSS
API
Stats

Use of this site constitutes acceptance of our User Agreement and Privacy Policy.

Powered by the version 2.3.6