#!/bin/bash set -e # ============================================================================= # Task 24: Multi-sample Variant Calling and Comparison # # DAG (depth 6, per-sample parallel then merge): # # L0: reads_A + reads_B + reference # L1: fastp A fastp B # L2: bwa A bwa B # L3: freebayes A freebayes B # L4: bcftools filter A bcftools filter B # └──────────┬───────────┘ # L5: bcftools isec (shared vs unique variants) # └── variant annotation + summary # L6: MERGE # ============================================================================= THREADS=$(( $(nproc) > 8 ? 8 : $(nproc) )) SCRIPT_DIR="$(cd "$(dirname "${BASH_SOURCE[0]}")" && pwd)" DATA="${SCRIPT_DIR}/data" REF="${SCRIPT_DIR}/reference" OUT="${SCRIPT_DIR}/outputs" RES="${SCRIPT_DIR}/results" REFERENCE="${REF}/reference.fna" SAMPLES=("sampleA" "sampleB") log_step() { echo "==================================================================" echo "STEP: $1" echo "$(date)" echo "==================================================================" } mkdir -p "${OUT}"/{trimmed,aligned,variants,filtered,comparison} "${RES}" # Per-sample processing (L1-L4) for SAMPLE in "${SAMPLES[@]}"; do # L1: Trim log_step "L1: fastp ${SAMPLE}" if [ ! -f "${OUT}/trimmed/${SAMPLE}_R1.fastq.gz" ]; then fastp --in1 "${DATA}/${SAMPLE}_R1.fastq.gz" --in2 "${DATA}/${SAMPLE}_R2.fastq.gz" \ --out1 "${OUT}/trimmed/${SAMPLE}_R1.fastq.gz" --out2 "${OUT}/trimmed/${SAMPLE}_R2.fastq.gz" \ --detect_adapter_for_pe --thread ${THREADS} \ --json "${OUT}/trimmed/${SAMPLE}_fastp.json" else echo "Skipping (exists)"; fi # L2: Align log_step "L2: bwa ${SAMPLE}" if [ ! -f "${OUT}/aligned/${SAMPLE}.bam" ]; then [ ! -f "${REFERENCE}.bwt" ] && bwa index "${REFERENCE}" 2>/dev/null bwa mem -t ${THREADS} -R "@RG\tID:${SAMPLE}\tSM:${SAMPLE}\tPL:ILLUMINA" \ "${REFERENCE}" "${OUT}/trimmed/${SAMPLE}_R1.fastq.gz" "${OUT}/trimmed/${SAMPLE}_R2.fastq.gz" \ | samtools sort -@ ${THREADS} -o "${OUT}/aligned/${SAMPLE}.bam" samtools index "${OUT}/aligned/${SAMPLE}.bam" else echo "Skipping (exists)"; fi # L3: Call variants log_step "L3: freebayes ${SAMPLE}" if [ ! -f "${OUT}/variants/${SAMPLE}.vcf" ]; then freebayes -f "${REFERENCE}" "${OUT}/aligned/${SAMPLE}.bam" \ --min-mapping-quality 20 --min-base-quality 20 \ > "${OUT}/variants/${SAMPLE}.vcf" else echo "Skipping (exists)"; fi # L4: Filter log_step "L4: bcftools filter ${SAMPLE}" if [ ! -f "${OUT}/filtered/${SAMPLE}.vcf.gz" ]; then bcftools filter -i 'QUAL>20 && INFO/DP>5' "${OUT}/variants/${SAMPLE}.vcf" \ | bcftools view -Oz -o "${OUT}/filtered/${SAMPLE}.vcf.gz" bcftools index "${OUT}/filtered/${SAMPLE}.vcf.gz" else echo "Skipping (exists)"; fi done # L5: Compare variants between samples log_step "L5: bcftools isec (shared vs unique)" if [ ! -d "${OUT}/comparison/isec" ]; then bcftools isec -p "${OUT}/comparison/isec" \ "${OUT}/filtered/sampleA.vcf.gz" \ "${OUT}/filtered/sampleB.vcf.gz" else echo "Skipping (exists)"; fi # Parse comparison results UNIQUE_A=$(grep -cv "^#" "${OUT}/comparison/isec/0000.vcf" 2>/dev/null || echo "0") UNIQUE_B=$(grep -cv "^#" "${OUT}/comparison/isec/0001.vcf" 2>/dev/null || echo "0") SHARED=$(grep -cv "^#" "${OUT}/comparison/isec/0002.vcf" 2>/dev/null || echo "0") # Per-sample stats VARS_A=$(bcftools stats "${OUT}/filtered/sampleA.vcf.gz" | grep "^SN" | grep "number of records" | cut -f4) VARS_B=$(bcftools stats "${OUT}/filtered/sampleB.vcf.gz" | grep "^SN" | grep "number of records" | cut -f4) SNPS_A=$(bcftools stats "${OUT}/filtered/sampleA.vcf.gz" | grep "^SN" | grep "number of SNPs" | cut -f4) SNPS_B=$(bcftools stats "${OUT}/filtered/sampleB.vcf.gz" | grep "^SN" | grep "number of SNPs" | cut -f4) # L6: MERGE log_step "L6-MERGE" cat > "${RES}/variant_comparison.csv" << CSVEOF metric,value total_variants_sampleA,${VARS_A} total_variants_sampleB,${VARS_B} snps_sampleA,${SNPS_A} snps_sampleB,${SNPS_B} unique_to_sampleA,${UNIQUE_A} unique_to_sampleB,${UNIQUE_B} shared_variants,${SHARED} CSVEOF echo "" echo "=== Pipeline complete ===" cat "${RES}/variant_comparison.csv"