Coverage Comparison Of Different Mappers
1
1
Entering edit mode
11.1 years ago
rob234king ▴ 610

Is there a tool or maybe a method in R to produce a line graph of the coverage of mapped resequencing, for each chromosome of the mapped bam file? I'm looking to compare the coverage across the genome of mapped reads using two different mapping software.

coverage • 2.4k views
ADD COMMENT
2
Entering edit mode
11.1 years ago

Do a simple loop with bash & samtools:

cut -d '       ' -f 1 reference.fa.fai |\
 while read CHROM
 do
     for BAM in *.bam
     do
         echo -n -e "${CHROM}\t${BAM}\t"
         samtools  view -F 4  -c ${BAM} ${CHROM}
     done
 done
ADD COMMENT
0
Entering edit mode

one-line command rocks !

ADD REPLY
0
Entering edit mode

I use your command from above (shown below) but remove some of the spaces in -d ' ' part to get it to work but I don't think my output looks correct? Seems to give me the total reads mapped for each chromosome (note chromosome 0 are a series of contigs which may explain why repeats it) but I'm thinking now that it would be more useful if I could do something more detailed like average coverage every 100 bases and print figure and average position so I could evaluate the coverage between the two mappers over different regions. Couldn't see an option in samtools to refine this command, any suggestions would be welcomed.

cut -d ' ' -f 1 /home/rob/Desktop/E9/samtoolsE9/S_lycopersicum.fa |\
 while read CHROM
 do
     for BAM in *.bam
     do
         echo -n -e "${CHROM}\t${BAM}\t"
         samtools view -F 4  -c ${BAM} ${CHROM}
     done
 done > /home/rob/Desktop/coverage1.vcf

Below is the output I'm getting

SL2.40ch00    A_BWA.marked.bam    17419246
SL2.40ch00    A_novoalign.marked.bam    13106767
AATAATAATAATAATAATAATAATAAATAAATAAATAAATAATAATAATAATAATAATAATAAATAAATAAATAAATAAA    A_BWA.marked.bam    17419246
AATAATAATAATAATAATAATAATAAATAAATAAATAAATAATAATAATAATAATAATAATAAATAAATAAATAAATAAA    A_novoalign.marked.bam    13106767
TAAATAAATAAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATA    A_BWA.marked.bam    17419246
TAAATAAATAAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATA    A_novoalign.marked.bam    13106767
ATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAAAAATAATAATAATAATAATAATAATAATAAT    A_BWA.marked.bam    17419246
ATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAATAAAAATAATAATAATAATAATAATAATAATAAT    A_novoalign.marked.bam    13106767
AATCATCATCATCATCATCATCATCATCATCATCATCATAATAATAATAATCATAATAAGGATAGATGATCTTTTCAACT    A_BWA.marked.bam    17419246
AATCATCATCATCATCATCATCATCATCATCATCATCATAATAATAATAATCATAATAAGGATAGATGATCTTTTCAACT    A_novoalign.marked.bam

Thanks

ADD REPLY

Login before adding your answer.

Traffic: 948 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