How to split vcf file by chromosome?

Question: How to split vcf file by chromosome?

2.9 years ago by

MAPK • 1.3k

United States

MAPK • 1.3k wrote:

I have tried several options on the web including a few post her on Biostar to split my VCF file by chromosome, but could not do it properly. Say I have a vcfile called myvcf.vcf.gz and want to split that per chromosome, what would be the best way to split it by chromosome?

vcf • 10k views

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modified 4 months ago by cartoonist • 30 • written 2.9 years ago by MAPK • 1.3k

ADD REPLY • link written 23 days ago by zx8754 ♦ 6.0k

2.9 years ago by

venu ♦ 5.7k

Germany

venu ♦ 5.7k wrote:

bgzip -c myvcf.vcf > myvcf.vcf.gz
tabix -p vcf myvcf.vcf.gz
tabix myvcf.vcf.gz chr1 > chr1.vcf

It will give chr1.vcf file containing variants for chr1. You can loop the last command over all the chromosomes. If you need vcf header also, use -h flag with last command.

ADD COMMENT • link modified 3 months ago by RamRS ♦ 19k • written 2.9 years ago by venu ♦ 5.7k

How do you extract chrX, chrY and chrM? Doesn't seem to work for those.

ADD REPLY • link written 2.3 years ago by MAPK • 1.3k

Then your chromosomes are either called something else or missing.

ADD REPLY • link written 7 months ago by Click downvote • 650

4 months ago by

cartoonist • 30

Germany

cartoonist • 30 wrote:

If the VCF file is tabix-indexed, extracting a subset by region name, let say chromosome 1, can be done by bcftools:

bcftools view -r 1 file.vcf.gz

ADD COMMENT • link written 4 months ago by cartoonist • 30

24 months ago by

ricardo • 20

Brazil/Fiocruz/Minas Gerais

ricardo • 20 wrote:

You can use the snpSift splitchr command. It separates a vcf file according to the chromosomes.

The command is simple:

java -jar snpSift splitChr file.vcf

ADD COMMENT • link modified 3 months ago by RamRS ♦ 19k • written 24 months ago by ricardo • 20

I dont know what version you used but right now this function is used like this :

  java -jar SnpSift.jar split file.vcf

great set of tools btw.

ADD REPLY • link modified 7 months ago • written 18 months ago by tiago211287 • 1.0k

9 months ago by

pyjiang2 • 30

United States

pyjiang2 • 30 wrote:

You can use vcftools. For example, if total 16 chromosomes

for i in {1..16};
do vcftools  --vcf  VCF_FILE  --chr $i  --recode --recode-INFO-all --out  VCF_$i;
done

ADD COMMENT • link modified 9 months ago • written 9 months ago by pyjiang2 • 30

2.3 years ago by

willgilks • 250

United Kingdom

willgilks • 250 wrote:

The question can be answered in a single command, using a bash loop to feed chromosome names into GATK's "select variants" command as shown below, whereby "-L" specifies which chromosome to select (https://software.broadinstitute.org/gatk/). This has the advantage over other methods in that index files are generated "on-the-fly". Also GATK is usually pretty robust. If using a genome with many chromosomes named e.g 1-22, users should modify the loop parameters, to something like "for i in seq 1 22;do"

for i in chr2L chr2R chr3L chr3R chr4 chrX;do
        GenomeAnalysisTK -R ${ref_seq} \
            -T SelectVariants \
            -V my_flies.vcf \
            -L $i \
                -o my_flies.${i}.vcf
                        done;

ADD COMMENT • link written 2.3 years ago by willgilks • 250

Is this a python script?

ADD REPLY • link written 18 months ago by kirannbishwa01 • 890

That's a bash loop executing a GATK java program.

ADD REPLY • link written 18 months ago by WouterDeCoster ♦ 35k

Thanks much ! Btw, I just stumbled upon https://gigabaseorgigabyte.wordpress.com/2017/05/02/an-orphan-bioinformatician/ while following your profile in biostars and then wordpress.

I am mainly a evolutionary biologist with a huge transition into Bioinformatics. If you would like to discuss about your problem I hope I can help, though I am not a full fledged programmer at this point. I have though managed to prepare a pipeline (or programme, whatever you may call it, lol) using python which is going to need a lots of cleaning and making it efficient, so I am learning. https://github.com/everestial/pHASE-Stitcher

Interesting fact is that I also consider myself a orphan bioinformatician (I like this word !). My situation was even terrible; I started PhD using genome and RNASeq data analyses, then came upon this problem of haplotype phasing in F1 hybrids, which wasn't solvable using any tools available. Additionally, there was null support on the matters of programming in my department and lab, but learning in a hardway has opened my pathway to writing my own program.

Your Biostars rep is quite high so I am thinking you might be quite ahead of me, but I think it would not hurt to discuss.

Thanks, - Bishwa K.

ADD REPLY • link written 18 months ago by kirannbishwa01 • 890

Thanks for reading. Feel free to comment on my blog post if you have suggestions, remarks or something else to add.

I have though managed to prepare a pipeline (or programme, whatever you may call it, lol) using python which is going to need a lots of cleaning and making it efficient, so I am learning. https://github.com/everestial/pHASE-Stitcher

That's the thing, you always keep learning and improving. Good luck writing your script!
Every now and then I have a look at old code and give it a makeover, it's surprising how much you learn in a few months.

ADD REPLY • link written 18 months ago by WouterDeCoster ♦ 35k

I think the best way to help and discuss is to put your tool on github (not matter how much small it might be). I just helps me or other people to create a branch and suggest the changes. Depending on how it works out for you or how it achieves the goal of the pipeline, you can merge it into the master branch.

Are you on github? Else, I have found these to be quite helpful :)

http://product.hubspot.com/blog/git-and-github-tutorial-for-beginners

https://git-scm.com/docs/git-push

https://github.com/cubeton/git101/tree/master/TurtorialInfo

ADD REPLY • link modified 18 months ago • written 18 months ago by kirannbishwa01 • 890

We are going fairly off topic here...
Thanks for the links, but I already have a github account and a few repositories.

ADD REPLY • link written 18 months ago by WouterDeCoster ♦ 35k

5 months ago by

ATpoint ♦ 10k

Germany

ATpoint ♦ 10k wrote:

You can use this code to split any VCF by all chromosomes present in the VCF, using parallel and tabix:

#!/bin/bash

## Assumes uncompressed VCF, extracts entries by chromosomes using tabix and parallel:
if [[ ${1: -4} != ".vcf" ]]
  then
  echo '[ERROR]: Please provide an uncompressed vcf file'
  exit; fi

## Get chromosomes that are present in the VCF:
cat $1 | mawk '$1 ~ /^#/ {next} {print $1 | "sort -k1,1 -u"}' > ${1%.vcf}_chrs.txt

## Compress & index file with tabix:
cat $1 | mawk '$1 ~ /^#/ {print $0;next} {print $0 | "sort -k1,1 -k2,2n"}' | bgzip -c > ${1%.vcf}_sorted.vcf.gz
tabix -p vcf ${1%.vcf}_sorted.vcf.gz

## Extract files by chr:
cat ${1%.vcf}_chrs.txt | parallel "tabix -h ${1%.vcf}_sorted.vcf.gz {} > ${1%.vcf}_{}.vcf"

## Usage: ./split_vcf_by_chr.sh input.vcf

ADD COMMENT • link modified 5 months ago • written 5 months ago by ATpoint ♦ 10k

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