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vg

tools for working with genome variation graphs

vg: variation graph tool, version v1.30.0 "Carentino"

usage: vg <command> [options]

graph construction
index graphs or alignments for random access or mapping
MEM-based read alignment
fast haplotype-aware short read alignment
augment a graph from an alignment
convert alignments to a compact coverage index
call or genotype VCF variants
show all subcommands

produce indexes for other subcommands
create a VCF from variation in the graph
build and manipulate GBWTs
manipulate node ids
build a minimizer index or a syncmer index
filter, transform, and edit the graph
prune the graph for GCSA2 indexing
simulate reads from a graph
compute snarls and their traversals
metrics describing graph and alignment properties
format conversions for graphs and alignments

add variants from a VCF to a graph
local alignment
annotate alignments with graphs and graphs with alignments
split graph or alignment into chunks
circularize a path within a graph
concatenate graphs tail-to-head
convert graphs between handle-graph compiant formats
estimate sequencing depth
generate the dotplot matrix from the embedded paths in an xg index
filter reads
compare alignment positions
compare multipath alignment positions
Sort a GAM file or index a sorted GAM file.
Genotype (or type) graphs, GAMS, and VCFs.
lift over alignments for the graph
multipath alignments of reads to a graph
traverse paths in the graph
construct spliced variation graphs and transcript paths
graph simplification
map alignments onto specific paths
trace haplotypes
transform alignments to simple ML-compatible vectors
render visualizations of indexed graphs and read sets

run and report on performance benchmarks
find and cluster mapping seeds
use an index to find nodes, edges, kmers, paths, or positions
Finds haplotypes based on reads using MCMC methods
run unit tests
validate the semantics of a graph or gam
version information

For technical support, please visit: https://www.biostars.org/t/vg/

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