bio-workflows-fastq-to-variants

name	bio-workflows-fastq-to-variants
description	End-to-end DNA sequencing workflow from FASTQ files to variant calls. Covers QC, alignment with BWA, BAM processing, and variant calling with bcftools or GATK HaplotypeCaller. Use when calling variants from raw sequencing reads.
tool_type	cli
primary_tool	bcftools
workflow	true
depends_on	["read-qc/fastp-workflow","read-alignment/bwa-alignment","alignment-files/alignment-sorting","alignment-files/duplicate-handling","variant-calling/variant-calling","variant-calling/filtering-best-practices"]
qc_checkpoints	[{"after_qc":"Q30 >85%, adapter content <1%"},{"after_alignment":"Mapping rate >95%, properly paired >90%"},{"after_dedup":"Duplication rate <30% for WGS, <50% for exome"},{"after_calling":"Ti/Tv ratio ~2.1 for WGS, dbSNP overlap >95%"}]

FASTQ to Variants Workflow

Complete pipeline from raw DNA sequencing FASTQ files to filtered variant calls.

Workflow Overview

FASTQ files
    |
    v
[1. QC & Trimming] -----> fastp
    |
    v
[2. Alignment] ---------> bwa-mem2
    |
    v
[3. BAM Processing] ----> sort, markdup, index
    |
    v
[4. Variant Calling] ---> bcftools (primary) or GATK
    |
    v
[5. Filtering] ---------> Quality filters
    |
    v
Filtered VCF

Primary Path: BWA + bcftools

Step 1: Quality Control with fastp

# Single sample
fastp -i sample_R1.fastq.gz -I sample_R2.fastq.gz \
    -o sample_R1.trimmed.fq.gz -O sample_R2.trimmed.fq.gz \
    --detect_adapter_for_pe \
    --qualified_quality_phred 20 \
    --length_required 50 \
    --html sample_fastp.html

# Batch processing
for sample in sample1 sample2 sample3; do
    fastp -i ${sample}_R1.fastq.gz -I ${sample}_R2.fastq.gz \
        -o trimmed/${sample}_R1.fq.gz -O trimmed/${sample}_R2.fq.gz \
        --detect_adapter_for_pe \
        --html qc/${sample}_fastp.html
done

QC Checkpoint 1: Check fastp reports

• Q30 bases >85% (DNA typically higher quality than RNA)
• Adapter content <1%
• No unusual GC distribution

Step 2: BWA-MEM2 Alignment

# Index reference (once)
bwa-mem2 index reference.fa

# Align with read group info
for sample in sample1 sample2 sample3; do
    bwa-mem2 mem -t 8 \
        -R "@RG\tID:${sample}\tSM:${sample}\tPL:ILLUMINA\tLB:lib1" \
        reference.fa \
        trimmed/${sample}_R1.fq.gz \
        trimmed/${sample}_R2.fq.gz \
    | samtools view -bS - > aligned/${sample}.bam
done

QC Checkpoint 2: Check alignment stats

samtools flagstat aligned/${sample}.bam

• Mapped reads >95%
• Properly paired >90%

Step 3: BAM Processing

for sample in sample1 sample2 sample3; do
    # Sort by coordinate
    samtools sort -@ 8 -o aligned/${sample}.sorted.bam aligned/${sample}.bam

    # Mark duplicates (samtools method)
    samtools fixmate -m aligned/${sample}.sorted.bam - | \
        samtools sort -@ 8 - | \
        samtools markdup -@ 8 - aligned/${sample}.markdup.bam

    # Index
    samtools index aligned/${sample}.markdup.bam

    # Cleanup intermediate
    rm aligned/${sample}.bam aligned/${sample}.sorted.bam
done

QC Checkpoint 3: Check duplication rate

samtools flagstat aligned/${sample}.markdup.bam | grep "duplicates"

• WGS: <30% duplicates
• Exome/targeted: <50% duplicates

Step 4: Variant Calling with bcftools

# Single sample calling
bcftools mpileup -Ou -f reference.fa aligned/sample1.markdup.bam | \
    bcftools call -mv -Oz -o variants/sample1.vcf.gz

# Multi-sample calling (joint calling)
bcftools mpileup -Ou -f reference.fa \
    aligned/sample1.markdup.bam \
    aligned/sample2.markdup.bam \
    aligned/sample3.markdup.bam | \
    bcftools call -mv -Oz -o variants/cohort.vcf.gz

bcftools index variants/cohort.vcf.gz

Step 5: Variant Filtering

# Basic quality filter
bcftools filter -Oz \
    -e 'QUAL<20 || DP<10 || MQ<30' \
    -o variants/cohort.filtered.vcf.gz \
    variants/cohort.vcf.gz

# More stringent filter
bcftools filter -Oz \
    -e 'QUAL<30 || DP<10 || DP>200 || MQ<40 || MQB<0.1' \
    -s "LowQual" \
    -o variants/cohort.filtered.vcf.gz \
    variants/cohort.vcf.gz

# Stats
bcftools stats variants/cohort.filtered.vcf.gz > variants/vcf_stats.txt

QC Checkpoint 4: Check variant stats

• Ti/Tv ratio ~2.1 for whole genome
• Ti/Tv ratio ~2.8-3.0 for exome

• 95% overlap with dbSNP for known sites

Alternative Path: BWA + GATK HaplotypeCaller

Step 4 Alternative: GATK Variant Calling

# Create sequence dictionary (once)
gatk CreateSequenceDictionary -R reference.fa

# Index reference (once)
samtools faidx reference.fa

# Base Quality Score Recalibration (BQSR)
gatk BaseRecalibrator \
    -R reference.fa \
    -I aligned/sample1.markdup.bam \
    --known-sites dbsnp.vcf.gz \
    -O recal_data.table

gatk ApplyBQSR \
    -R reference.fa \
    -I aligned/sample1.markdup.bam \
    --bqsr-recal-file recal_data.table \
    -O aligned/sample1.recal.bam

# HaplotypeCaller (per-sample GVCF mode)
gatk HaplotypeCaller \
    -R reference.fa \
    -I aligned/sample1.recal.bam \
    -O variants/sample1.g.vcf.gz \
    -ERC GVCF

# Joint genotyping (for multiple samples)
gatk GenomicsDBImport \
    -V variants/sample1.g.vcf.gz \
    -V variants/sample2.g.vcf.gz \
    -V variants/sample3.g.vcf.gz \
    --genomicsdb-workspace-path genomicsdb \
    -L intervals.bed

gatk GenotypeGVCFs \
    -R reference.fa \
    -V gendb://genomicsdb \
    -O variants/cohort.vcf.gz

Step 5 Alternative: GATK Variant Filtering

# Hard filtering (for small cohorts)
gatk VariantFiltration \
    -R reference.fa \
    -V variants/cohort.vcf.gz \
    --filter-expression "QD < 2.0" --filter-name "LowQD" \
    --filter-expression "FS > 60.0" --filter-name "HighFS" \
    --filter-expression "MQ < 40.0" --filter-name "LowMQ" \
    --filter-expression "MQRankSum < -12.5" --filter-name "LowMQRS" \
    --filter-expression "ReadPosRankSum < -8.0" --filter-name "LowRPRS" \
    -O variants/cohort.filtered.vcf.gz

# VQSR (for large cohorts >30 samples)
gatk VariantRecalibrator \
    -R reference.fa \
    -V variants/cohort.vcf.gz \
    --resource:hapmap,known=false,training=true,truth=true,prior=15.0 hapmap.vcf.gz \
    --resource:omni,known=false,training=true,truth=false,prior=12.0 omni.vcf.gz \
    --resource:1000G,known=false,training=true,truth=false,prior=10.0 1000G.vcf.gz \
    --resource:dbsnp,known=true,training=false,truth=false,prior=2.0 dbsnp.vcf.gz \
    -an QD -an MQ -an MQRankSum -an ReadPosRankSum -an FS -an SOR \
    -mode SNP \
    -O cohort.snp.recal \
    --tranches-file cohort.snp.tranches

gatk ApplyVQSR \
    -R reference.fa \
    -V variants/cohort.vcf.gz \
    -O variants/cohort.vqsr.vcf.gz \
    --recal-file cohort.snp.recal \
    --tranches-file cohort.snp.tranches \
    -mode SNP \
    --truth-sensitivity-filter-level 99.5

Parameter Recommendations

Step	Parameter	WGS	Exome/Targeted
bwa-mem2	-t	8-16	8
samtools markdup	-	Required	Required
bcftools mpileup	-d	250 (default)	1000
bcftools mpileup	-q	20	20
bcftools filter	QUAL	>20	>30
bcftools filter	DP	>10, <2x mean	>20
GATK	intervals	-	Target BED

Choosing Between bcftools and GATK

Criterion	bcftools	GATK
Speed	Faster	Slower
Memory	Lower	Higher
Best for	Germline SNPs/indels	Germline, somatic
Cohort size	Any	Scales well
BQSR	Not supported	Recommended
VQSR	Not supported	For large cohorts

Troubleshooting

Issue	Likely Cause	Solution
Low mapping rate	Wrong reference, contamination	Verify reference genome version
High duplication	PCR over-amplification, low input	Check library prep, may need more input DNA
Low Ti/Tv	False positives	Increase quality filters
Missing variants	Too stringent filters, low depth	Relax filters, check coverage
Many indels at homopolymers	Sequencing errors	Filter homopolymer regions

Complete Pipeline Script

#!/bin/bash
set -e

# Configuration
THREADS=8
REF="reference.fa"
SAMPLES="sample1 sample2 sample3"
OUTDIR="results"

mkdir -p ${OUTDIR}/{trimmed,aligned,variants,qc}

echo "=== Step 1: QC with fastp ==="
for sample in $SAMPLES; do
    fastp -i ${sample}_R1.fastq.gz -I ${sample}_R2.fastq.gz \
        -o ${OUTDIR}/trimmed/${sample}_R1.fq.gz \
        -O ${OUTDIR}/trimmed/${sample}_R2.fq.gz \
        --detect_adapter_for_pe \
        --html ${OUTDIR}/qc/${sample}_fastp.html \
        -w ${THREADS}
done

echo "=== Step 2: Alignment with bwa-mem2 ==="
for sample in $SAMPLES; do
    bwa-mem2 mem -t ${THREADS} \
        -R "@RG\tID:${sample}\tSM:${sample}\tPL:ILLUMINA" \
        ${REF} \
        ${OUTDIR}/trimmed/${sample}_R1.fq.gz \
        ${OUTDIR}/trimmed/${sample}_R2.fq.gz | \
    samtools view -@ ${THREADS} -bS - > ${OUTDIR}/aligned/${sample}.bam
done

echo "=== Step 3: BAM Processing ==="
for sample in ; 
    samtools fixmate -@  -m /aligned/.bam - | \
    samtools  -@  - | \
    samtools markdup -@  - /aligned/.markdup.bam
    samtools index /aligned/.markdup.bam
     /aligned/.bam


 
bcftools mpileup -Ou -f  /aligned/*.markdup.bam | \
    bcftools call - -Oz -o /variants/cohort.vcf.gz
bcftools index /variants/cohort.vcf.gz

 
bcftools filter -Oz \
    -e  \
    -o /variants/cohort.filtered.vcf.gz \
    /variants/cohort.vcf.gz
bcftools index /variants/cohort.filtered.vcf.gz

 
bcftools stats /variants/cohort.filtered.vcf.gz > /variants/stats.txt

 
 

Related Skills

• read-qc/fastp-workflow - Detailed QC options
• read-alignment/bwa-alignment - BWA-MEM2 parameters
• alignment-files/duplicate-handling - Duplicate marking details
• variant-calling/variant-calling - bcftools calling options
• variant-calling/gatk-variant-calling - GATK HaplotypeCaller details
• variant-calling/filtering-best-practices - Advanced filtering strategies
• variant-calling/variant-annotation - Annotate variants with VEP