jvarkit

ReferenceToVCF

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Creates a VCF containing all the possible substitutions from a Reference Genome.

Usage

This program is now part of the main jvarkit tool. See jvarkit for compiling.

Usage: java -jar dist/jvarkit.jar fasta2vcf  [options] Files

Usage: fasta2vcf [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
    -L, --bed
      limit to this BED
    -d, --deletions
      generate deletions
      Default: 0
    -A, --disjoint
      disjoint ALT. Write one variant per ALT for SNVs
      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].
    -i, --insertions
      generate insertions
      Default: 0
    -o, --output
      Output file. Optional . Default: stdout
    --version
      print version and exit

Keywords

Creation Date

20140910

Source code

https://github.com/lindenb/jvarkit/tree/master/src/main/java/com/github/lindenb/jvarkit/tools/ref2vcf/ReferenceToVCF.java

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License

The project is licensed under the MIT license.

Citing

Should you cite fasta2vcf ? 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