README.md

vcfstats - powerful statistics for VCF files

Documentation | CHANGELOG

Motivation

There are a couple of tools that can plot some statistics of VCF files, including bcftools and jvarkit. However, none of them could:

1. plot specific metrics
2. customize the plots
3. focus on variants with certain filters

R package vcfR can do some of the above. However, it has to load entire VCF into memory, which is not friendly to large VCF files.

Installation

pip install -U vcfstats

Or run with docker:

docker run \
  -w /vcfstats/workdir \
  -v $(pwd):/vcfstats/workdir \
  --rm justold/vcfstats:latest \
  vcfstats \
  --vcf myfile.vcf \
  -o outputs \
  --formula 'COUNT(1) ~ CONTIG' \
  --title 'Number of variants on each chromosome'

Gallery

Number of variants on each chromosome

vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    --formula 'COUNT(1) ~ CONTIG' \
    --title 'Number of variants on each chromosome' \
    --config examples/config.toml

Changing labels and ticks

vcfstats uses plotnine for plotting, read more about it on how to specify --ggs to modify the plots.

vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    --formula 'COUNT(1) ~ CONTIG' \
    --title 'Number of variants on each chromosome (modified)' \
    --config examples/config.toml \
    --ggs 'scale_x_discrete(name ="Chromosome", \
        limits=["1","2","3","4","5","6","7","8","9","10","X"]); \
        ylab("# Variants")'

Number of variants on first 5 chromosome

vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    --formula 'COUNT(1) ~ CONTIG[1,2,3,4,5]' \
    --title 'Number of variants on each chromosome (first 5)' \
    --config examples/config.toml
# or
vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    --formula 'COUNT(1) ~ CONTIG[1-5]' \
    --title 'Number of variants on each chromosome (first 5)' \
    --config examples/config.toml
# or
# require vcf file to be tabix-indexed.
vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    --formula 'COUNT(1) ~ CONTIG' \
    --title 'Number of variants on each chromosome (first 5)' \
    --config examples/config.toml -r 1 2 3 4 5

Number of substitutions of SNPs

vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    --formula 'COUNT(1, VARTYPE[snp]) ~ SUBST[A>T,A>G,A>C,T>A,T>G,T>C,G>A,G>T,G>C,C>A,C>T,C>G]' \
    --title 'Number of substitutions of SNPs' \
    --config examples/config.toml

Only with SNPs PASS all filters

vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    --formula 'COUNT(1, VARTYPE[snp]) ~ SUBST[A>T,A>G,A>C,T>A,T>G,T>C,G>A,G>T,G>C,C>A,C>T,C>G]' \
    --title 'Number of substitutions of SNPs (passed)' \
    --config examples/config.toml \
    --passed

Alternative allele frequency on each chromosome

# using a dark theme
vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    --formula 'AAF ~ CONTIG' \
    --title 'Allele frequency on each chromosome' \
    --config examples/config.toml --ggs 'theme_dark()'

Using boxplot

vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    --formula 'AAF ~ CONTIG' \
    --title 'Allele frequency on each chromosome (boxplot)' \
    --config examples/config.toml \
    --figtype boxplot

Using density plot/histogram to investigate the distribution:

You can plot the distribution, using density plot or histogram

vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    --formula 'AAF ~ CONTIG[1,2]' \
    --title 'Allele frequency on chromosome 1,2' \
    --config examples/config.toml \
    --figtype density

Overall distribution of allele frequency

vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    --formula 'AAF ~ 1' \
    --title 'Overall allele frequency distribution' \
    --config examples/config.toml

Excluding some low/high frequency variants

vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    --formula 'AAF[0.05, 0.95] ~ 1' \
    --title 'Overall allele frequency distribution (0.05-0.95)' \
    --config examples/config.toml

Counting types of variants on each chromosome

vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    --formula 'COUNT(1, group=VARTYPE) ~ CHROM' \
    # or simply
    # --formula 'VARTYPE ~ CHROM' \
    --title 'Types of variants on each chromosome' \
    --config examples/config.toml

Using bar chart if there is only one chromosome

vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    --formula 'COUNT(1, group=VARTYPE) ~ CHROM[1]' \
    # or simply
    # --formula 'VARTYPE ~ CHROM[1]' \
    --title 'Types of variants on chromosome 1' \
    --config examples/config.toml \
    --figtype pie

Counting variant types on whole genome

vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    # or simply
    # --formula 'VARTYPE ~ 1' \
    --formula 'COUNT(1, group=VARTYPE) ~ 1' \
    --title 'Types of variants on whole genome' \
    --config examples/config.toml

Counting type of mutant genotypes (HET, HOM_ALT) for sample 1 on each chromosome

vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    # or simply
    # --formula 'GTTYPEs[HET,HOM_ALT]{0} ~ CHROM' \
    --formula 'COUNT(1, group=GTTYPEs[HET,HOM_ALT]{0}) ~ CHROM' \
    --title 'Mutant genotypes on each chromosome (sample 1)' \
    --config examples/config.toml

Exploration of mean(genotype quality) and mean(depth) on each chromosome for sample 1

vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    --formula 'MEAN(GQs{0}) ~ MEAN(DEPTHs{0}, group=CHROM)' \
    --title 'GQ vs depth (sample 1)' \
    --config examples/config.toml

Exploration of depths for sample 1,2

vcfstats --vcf examples/sample.vcf \
    --outdir examples/ \
    --formula 'DEPTHs{0} ~ DEPTHs{1}' \
    --title 'Depths between sample 1 and 2' \
    --config examples/config.toml

See more examples:

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