Concatenate VCFs with same sample. See also bcftools concat
This program is now part of the main jvarkit
tool. See jvarkit for compiling.
Usage: java -jar dist/jvarkit.jar vcfconcat [options] Files
Usage: vcfconcat [options] Files
Options:
--bcf-output
If this program writes a VCF to a file, The format is first guessed from
the file suffix. Otherwise, force BCF output. The current supported BCF
version is : 2.1 which is not compatible with bcftools/htslib (last
checked 2019-11-15)
Default: false
--chrom, --contig
limit to that chromosome
-G, --drop-genotypes
Drop genotypes
Default: false
--generate-vcf-md5
Generate MD5 checksum for VCF output.
Default: false
-h, --help
print help and exit
--helpFormat
What kind of help. One of [usage,markdown,xml].
--merge
merge all samples. First Scan all files to get all distinct samples
Default: false
-o, --out
Output file. Optional . Default: stdout
-S, --samples
implies --drop-genotypes
Default: none
Possible Values: [none, all, with_alt]
-T, --tag
if not empty, add INFO/tag containing the source/path of the variant
Default: <empty string>
--version
print version and exit
20131230
The project is licensed under the MIT license.
Should you cite vcfconcat ? https://github.com/mr-c/shouldacite/blob/master/should-I-cite-this-software.md
The current reference is:
http://dx.doi.org/10.6084/m9.figshare.1425030
Lindenbaum, Pierre (2015): JVarkit: java-based utilities for Bioinformatics. figshare. http://dx.doi.org/10.6084/m9.figshare.1425030
concat numerous VCF, without checking files at start, doesn’t sort.
input is a set of VCF files or a file with the suffix .list containing the path to the vcfs
$ find ./ -name "*.vcf" | grep Sample1 | java -jar dist/jvarkit vcfconcat > out.vcf
$ java -jar dist/jvarkit vcfconcat Sample1.samtools.vcf Sample1.gatk.vcf > out.vcf
$ java -jar dist/jvarkit vcfconcat paths.list > out.vcf
bcftools concat