Fisher Case / Controls per Variant (Vertical)
Usage: vcfburdenfisherv [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
--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].
-if, --ignorefilter
accept variants having a FILTER column. Default is ignore variants with
a FILTER column
Default: false
-o, --output
Output file. Optional . Default: stdout
* -p, --pedigree
A pedigree file. tab delimited. Columns: family,id,father,mother,
sex:(0:unknown;1:male;2:female), phenotype
(-9|?|.:unknown;1|affected|case:affected;0|unaffected|control:unaffected)
-table, --table
Write statistics into that file instead of the VCF (faster)
--version
print version and exit
${PATH}
. Setting JAVA_HOME is not enough : (e.g: https://github.com/lindenb/jvarkit/issues/23 )$ git clone "https://github.com/lindenb/jvarkit.git"
$ cd jvarkit
$ ./gradlew vcfburdenfisherv
The java jar file will be installed in the dist
directory.
20160418
The project is licensed under the MIT license.
Should you cite vcfburdenfisherv ? 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
Variant in that VCF should have one and only one ALT allele. Use https://github.com/lindenb/jvarkit/wiki/VcfMultiToOneAllele if needed.