Creates a VCF containing all the possible substitutions from a Reference Genome.
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
20140910
The project is licensed under the MIT license.
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