bcftools-variant-manipulation

name	bcftools-variant-manipulation
description	CLI for VCF/BCF: filter, merge, annotate, query, normalize, compute stats. Core post-variant-calling: quality filtering, multi-sample merging, rsID annotation, genotype extraction. Samtools companion in HTSlib. Use GATK for complex indel realignment during calling; use VCFtools for population genetics stats.
license	MIT

bcftools — VCF/BCF Variant Manipulation Toolkit

Overview

bcftools is the standard command-line toolkit for processing VCF (Variant Call Format) and BCF (Binary Call Format) files in the HTSlib ecosystem. It covers the complete post-variant-calling workflow: format conversion, quality filtering, variant normalization, multi-sample merging, annotation with external databases, genotype extraction, and QC statistics. bcftools uses streaming by design — most commands read from stdin and write to stdout, making it ideal for memory-efficient pipelines on large cohorts.

When to Use

• Filtering variants by quality (QUAL, DP, AF) after variant calling
• Merging VCF files from multiple samples into a joint call set
• Adding rsIDs or gene annotations to variant calls
• Extracting specific fields (genotypes, allele depths) as tabular output
• Normalizing indel representations and splitting multi-allelic records
• Calling variants from pileup output (mpileup + call)
• Computing per-sample and overall VCF QC statistics
• Use GATK HaplotypeCaller instead when calling variants with local realignment in human samples
• Use VCFtools instead for population genetics statistics (Fst, LD, Hardy-Weinberg)
• Use bcftools in the HTSlib pipeline; use picard for duplicate-marking and library metrics

Prerequisites

• Installation: bcftools 1.17+ (part of HTSlib suite with samtools)
• Input requirements: VCF or BGzipped+tabix-indexed VCF (.vcf.gz + .vcf.gz.tbi) for region queries
• Companion tools: samtools for BAM processing; tabix for VCF indexing

Check before installing: The tool may already be available in the current environment (e.g., inside a pixi / conda env). Run command -v bcftools first and skip the install commands below if it returns a path. When running inside a pixi project, invoke the tool via pixi run bcftools rather than bare bcftools.

# Bioconda (recommended — installs HTSlib suite)
conda install -c bioconda bcftools

# Homebrew (macOS)
brew install bcftools

# Verify
bcftools --version | head -1
# bcftools 1.20

# Index a VCF for region queries
bcftools index -t variants.vcf.gz   # creates .tbi
bcftools index -c variants.vcf.gz   # creates .csi (for chromosomes > 512 Mb)

Quick Start

# Typical post-calling workflow: normalize → filter → annotate → extract
bcftools norm -d any -f reference.fa variants.vcf.gz \
  | bcftools filter -i 'QUAL>20 && DP>10' \
  | bcftools annotate -a dbSNP.vcf.gz -c ID \
  | bcftools view -O z -o final.vcf.gz

# Index the output
bcftools index -t final.vcf.gz

# Count variants at each stage
bcftools stats final.vcf.gz | grep "^SN"

Core API

Module 1: VCF/BCF I/O and Format Conversion

Convert between text VCF and binary BCF; compress and index for random access.

# VCF → compressed BCF (fastest format for piping)
bcftools view -O b -o variants.bcf variants.vcf

# BCF → VCF (for human-readable output)
bcftools view -O v -o variants.vcf variants.bcf

# VCF → bgzipped + indexed (standard archive format)
bcftools view -O z -W -o variants.vcf.gz variants.vcf
# -W automatically creates .tbi index after writing

# Extract specific samples
bcftools view -s sample1,sample2 -O z -o subset.vcf.gz variants.vcf.gz

# Exclude samples (prefix with ^)
bcftools view -s ^outlier_sample -O z -o cleaned.vcf.gz variants.vcf.gz

# Extract by region (fast; requires index)
bcftools view -r chr1:1000000-2000000 variants.vcf.gz -O v -o chr1_region.vcf

# Streaming pipeline: no intermediate files
samtools mpileup -Ou input.bam | bcftools call -m -Oz -o calls.vcf.gz

Module 2: Variant Filtering

Apply quality thresholds and FLAG-based filters to retain high-confidence calls.

# Expression-based filter (include)
bcftools filter -i 'QUAL>20 && DP>10' variants.vcf.gz -O z -o filtered.vcf.gz

# Expression-based filter (exclude)
bcftools filter -e 'QUAL<10 || DP<5' variants.vcf.gz -O v -o filtered.vcf

# Soft filter: mark but keep (sets FILTER field to label)
bcftools filter -s LowQual -e 'QUAL<20' variants.vcf.gz -O z -o soft_filtered.vcf.gz
# Variants with QUAL<20 get FILTER="LowQual"; others get FILTER=PASS

# Keep only PASS variants
bcftools view -f PASS variants.vcf.gz -O z -o pass_only.vcf.gz

# SNP-only output
bcftools view --type snps variants.vcf.gz -O z -o snps.vcf.gz

# Indel-only output
bcftools view --type indels variants.vcf.gz -O z -o indels.vcf.gz

# Filter by allele frequency and depth
bcftools filter -i 'AF>0.1 && DP>20 && MQ>40' variants.vcf.gz -O z -o confident.vcf.gz

# Remove SNPs within 3 bp of indels
bcftools filter --SnpGap 3 variants.vcf.gz -O z -o gapfiltered.vcf.gz

Module 3: VCF Query and Extraction

Transform VCF content into tabular text for downstream analysis.

# Extract chrom, position, ref, alt, quality
bcftools query -f '%CHROM\t%POS\t%REF\t%ALT\t%QUAL\n' variants.vcf.gz > variants.txt

# With header row (-H adds #-prefixed column names)
bcftools query -H -f '%CHROM\t%POS\t%REF\t%ALT\t%QUAL\n' variants.vcf.gz > variants.tsv

# Per-sample genotypes and allele depths
bcftools query -f '[%SAMPLE\t%GT\t%AD\n]' variants.vcf.gz > genotypes.txt
# Output: sample1  0/1  25,18  (ref_depth,alt_depth)

# Rare variants (AF < 1%)
bcftools query -i 'AF<0.01' -f '%CHROM\t%POS\t%REF\t%ALT\t%AF\n' \
    variants.vcf.gz > rare_variants.txt

# Count variants per chromosome
bcftools query -f '%CHROM\n' variants.vcf.gz | sort | uniq -c | sort -rn

# Extract genotype matrix across all samples
bcftools query -f '%CHROM:%POS\t[%GT\t]\n' -H variants.vcf.gz > genotype_matrix.tsv

Module 4: Multi-file Operations

Combine VCF files from multiple samples (merge) or chromosomes (concat).

# Merge: join VCFs from DIFFERENT sample sets (same variants)
bcftools merge sample1.vcf.gz sample2.vcf.gz sample3.vcf.gz \
    -O z -o cohort.vcf.gz

# Merge with auto-indexing and threading
bcftools merge -O b -W --threads 4 sample*.vcf.gz > cohort.bcf

# Concat: join VCFs from SAME sample set (different chromosomes or batches)
bcftools concat chr1.vcf.gz chr2.vcf.gz chr3.vcf.gz -O z -o full.vcf.gz

# Concat with overlap handling (from batched calling)
bcftools concat -a --threads 4 batch*.vcf.gz -O z -o concat.vcf.gz

# Pipeline: merge → filter → normalize
bcftools merge sample1.vcf.gz sample2.vcf.gz \
    | bcftools filter -i 'QUAL>20' \
    | bcftools norm -d any -f genome.fa \
    | bcftools view -O z -o merged_clean.vcf.gz
bcftools index -t merged_clean.vcf.gz

# Extract genotype matrix from merged cohort
bcftools merge cohort*.vcf.gz | bcftools query -f '[%GT\t]\n' > gt_matrix.tsv

Module 5: Variant Annotation

Add identifiers, gene annotations, or external data to VCF records.

# Add rsIDs from dbSNP
bcftools annotate -a dbSNP.vcf.gz -c ID variants.vcf.gz -O z -o rsid_annotated.vcf.gz

# Annotate with BED file (adds gene names)
bcftools annotate -a genes.bed.gz \
    -h <(echo '##INFO=<ID=GENE,Number=1,Type=String,Description="Gene name">') \
    -c CHROM,FROM,TO,GENE \
    variants.vcf.gz -O z -o gene_annotated.vcf.gz

# Remove unwanted INFO fields
bcftools annotate -x INFO/AC,INFO/AN,INFO/MQ variants.vcf.gz -O v -o stripped.vcf

# Normalize: left-align indels, split multi-allelic records
bcftools norm -f reference.fa variants.vcf.gz -O v -o normalized.vcf

# Split multi-allelic sites into separate records
bcftools norm -m -any variants.vcf.gz -O v -o split.vcf

# Deduplicate overlapping records
bcftools norm -d any variants.vcf.gz -O z -o deduped.vcf.gz

# Full normalize pipeline
bcftools norm -m -any variants.vcf.gz | \
    bcftools norm -d any -f reference.fa | \
    bcftools view -O z -o normalized_split.vcf.gz

Module 6: Statistics and QC

Generate summary metrics and per-sample variant counts.

# Full VCF statistics report
bcftools stats variants.vcf.gz > qc.stats.txt

# Extract Summary Numbers section only
grep "^SN" qc.stats.txt | cut -f3,4
# number of records:    45231
# number of SNPs:       38941
# number of indels:     6290
# ...

# Per-sample stats (PSC = per-sample counts)
bcftools stats -s - variants.vcf.gz | grep "^PSC" > per_sample.txt
# cols: id  sample  hom_RR  het  hom_AA  ts  tv  indel  missing  singleton

# Transition/transversion ratio (genome-wide QC)
bcftools stats variants.vcf.gz | grep "Ts/Tv"
# Ts/Tv ratio: 2.06 (healthy WGS; <1.8 or >2.2 suggests quality issues)

# Check for sample contamination (F-statistic per sample)
bcftools stats -s - variants.vcf.gz | grep "^PSC" | awk '{print $2, $9}'
# sample  F_missing (high = poor sample quality)

# Variant calling (mpileup → call pipeline)
samtools mpileup -Ou -f genome.fa *.bam | bcftools call -m -v -Oz -o calls.vcf.gz
bcftools stats calls.vcf.gz | grep "^SN"

Key Concepts

Output Format Flags

-O v  → VCF text (uncompressed)       default for human inspection
-O z  → bgzipped VCF (.vcf.gz)        standard for archiving
-O b  → binary BCF (compressed)        fastest for piping
-O u  → binary BCF (uncompressed)      fastest output (no compression)

Rule: Use -O b or -O u for intermediate pipeline steps (no I/O overhead). Use -O z for files you will store or index with tabix.

Filter Expression Syntax

Expressions use INFO and FORMAT fields with comparison operators:

# INFO fields (one value per variant)
QUAL>20          # quality score
DP>10            # total depth
AF<0.05          # allele frequency
MQ>40            # mapping quality

# FORMAT fields (per-sample; use [] to iterate)
GT=="1/1"        # homozygous alternate
AD[1]>5          # alt allele depth > 5
GQ>20            # genotype quality

# Combined
QUAL>20 && DP>10 && AF>0.01
(GT=="0/0" || GT=="1/1") && GQ>30

Common Workflows

Workflow 1: Variant QC and Filtering Pipeline

Goal: Normalize, filter, and annotate a raw variant call set for downstream analysis.

#!/bin/bash
VCF="raw_calls.vcf.gz"
REF="reference.fa"
DBSNP="dbSNP_hg38.vcf.gz"
FINAL="variants_filtered_annotated.vcf.gz"

# 1. Normalize: left-align indels, split multi-allelic, deduplicate
bcftools norm -m -any $VCF \
    | bcftools norm -d any -f $REF \
    | bcftools view -O z -o normalized.vcf.gz
bcftools index -t normalized.vcf.gz

# 2. Filter by quality and depth
bcftools filter -i 'QUAL>20 && DP>10' normalized.vcf.gz \
    | bcftools filter --SnpGap 3 \
    | bcftools view -f PASS -O z -o filtered.vcf.gz
bcftools index -t filtered.vcf.gz

# 3. Annotate with rsIDs
bcftools annotate -a $DBSNP -c ID filtered.vcf.gz -O z -o $FINAL
bcftools index -t $FINAL

# Report variant counts
echo "Final variant count:"
bcftools stats $FINAL | grep "number of records"

Workflow 2: Multi-sample Cohort Merging and Genotype Extraction

Goal: Merge per-sample VCFs into a cohort VCF; extract a genotype matrix for GWAS.

#!/bin/bash
SAMPLES=(sample1 sample2 sample3 sample4 sample5)

# 1. Ensure all VCFs are indexed
for s in "${SAMPLES[@]}"; do
    bcftools index -t ${s}.vcf.gz
done

# 2. Merge into cohort VCF (only sites present in ALL samples: -m none)
bcftools merge -m none "${SAMPLES[@]/%/.vcf.gz}" \
    -O z --threads 8 -o cohort.vcf.gz
bcftools index -t cohort.vcf.gz

# 3. Filter: PASS, SNPs only, MAF > 1%
bcftools view -f PASS --type snps cohort.vcf.gz \
    | bcftools filter -i 'AF>0.01 && AF<0.99' \
    | bcftools view -O z -o cohort_snps_filtered.vcf.gz

# 4. Extract numeric genotype matrix (for plink/R/Python)
bcftools query -H \
    -f '%CHROM\t%POS\t%REF\t%ALT\t[%GT\t]\n' \
    cohort_snps_filtered.vcf.gz > genotype_matrix.tsv
echo "Genotype matrix: $(wc -l < genotype_matrix.tsv) variants x ${#SAMPLES[@]} samples"

Key Parameters

Parameter	Command	Default	Range/Options	Effect
-O	Most	v	v,z,b,u	Output format: VCF, bgzip-VCF, BCF, uncompressed BCF
-r	Most	—	chr:pos-end	Region filter (requires tabix index)
-s	Most	All	sample names	Include specific samples (prefix ^ to exclude)
-i	filter	—	expression	Include variants matching expression
-e	filter	—	expression	Exclude variants matching expression
-f	query	—	format string	Custom output format string
--threads	Most	1	1–N	Compression/decompression threads
-a	annotate	—	file path	Annotation source (BED, VCF, TSV)
-m	norm	none	-any, +any	Split (−) or join (+) multi-allelic records
-d	norm	—	all,any,snps	Deduplication strategy
-W	view	—	flag	Auto-create index after writing
-v	call	—	flag	Output variant sites only (skip reference sites)

Best Practices

1. Index before region queries: bcftools view -r chr1:... requires a .tbi or .csi index. Always run bcftools index -t output.vcf.gz after creating any bgzipped VCF.

2. Normalize before merging or annotation: Different callers represent the same indel differently. Run bcftools norm -m -any | bcftools norm -d any -f ref.fa before merging to prevent duplicate records.

3. Use -O u for pipeline intermediates: Uncompressed BCF output (-O u) eliminates compression/decompression overhead in multi-step pipes — typically 2-3× faster than -O z.

4. Verify Ts/Tv ratio after calling: bcftools stats variants.vcf.gz | grep Ts/Tv. For human WGS, expect 2.0–2.1; exome 2.5–3.0. Values outside these ranges indicate quality problems.

5. Filter before merge for large cohorts: Filtering per-sample VCFs before merging reduces memory and I/O. Apply site-level QC (QUAL>20 && DP>5) to each sample before bcftools merge.

6. Check chromosome naming consistency: bcftools fails silently if merging chr1-style with 1-style VCFs. Verify with bcftools view -h file.vcf.gz | grep "^##contig".

Common Recipes

Recipe: Count Variants Before and After Filtering

echo "Before:" $(bcftools view -c 1 raw.vcf.gz | wc -l)
echo "PASS only:" $(bcftools view -f PASS raw.vcf.gz | bcftools view -c 1 | wc -l)
echo "SNPs PASS:" $(bcftools view -f PASS --type snps raw.vcf.gz | bcftools view -c 1 | wc -l)

Recipe: Extract Heterozygous Sites for One Sample

bcftools view -s SAMPLE_A variants.vcf.gz \
    | bcftools filter -i 'GT="0/1"' \
    | bcftools query -f '%CHROM\t%POS\t%REF\t%ALT\n' > het_sites.txt
echo "$(wc -l < het_sites.txt) heterozygous sites"

Recipe: Compare Two VCF Files for Concordance

# Find variants unique to each file and shared
bcftools isec -p isec_dir file1.vcf.gz file2.vcf.gz
ls isec_dir/
# 0000.vcf: private to file1
# 0001.vcf: private to file2
# 0002.vcf: shared (from file1 perspective)
# 0003.vcf: shared (from file2 perspective)
echo "Shared: $(wc -l < isec_dir/0002.vcf) variants"

Troubleshooting

Problem	Cause	Solution
Missing index error	VCF not indexed (needed for -r region queries)	Run bcftools index -t file.vcf.gz
[E::vcf_parse_format] parse error	Malformed VCF FORMAT or INFO field	Validate: bcftools view file.vcf.gz 2>&1 | head -5; check source tool version
Empty filter output	Expression too strict or field missing	Test expression: bcftools view -h file.vcf.gz | grep "##INFO=<ID=QUAL"
Merge: sample duplication	Duplicate sample names across input VCFs	Rename with bcftools reheader -s new_names.txt sample.vcf.gz before merging
Wrong Ts/Tv ratio (<1.8)	Low-quality calls or poor coverage	Apply stricter quality filter (QUAL>30 && DP>15); check alignment quality
concat fails with overlap	Overlapping regions in input VCFs	Use -a flag: bcftools concat -a file1.vcf.gz file2.vcf.gz
Annotation mismatch	chr naming conflict (chr1 vs 1)	Check: bcftools view -h file.vcf.gz | grep contig; rename with bcftools annotate --rename-chrs
query returns empty fields	FORMAT field not populated for sample	Check VCF header: bcftools view -h file.vcf.gz | grep FORMAT

Related Skills

• samtools-bam-processing — BAM processing that feeds into bcftools variant calling pipeline
• bedtools-genomic-intervals — intersecting VCF variants with genomic features (genes, regions)
• gget-genomic-databases — Ensembl/NCBI queries to annotate variant gene context

References

• bcftools documentation — complete command reference
• GitHub: samtools/bcftools — source code, releases, issue tracker
• Danecek et al. (2021) "Twelve years of SAMtools and BCFtools" — GigaScience 10(2)
• VCF file format specification — field definitions and encoding rules