Genomics Analysis Guide

Raw FASTQ files
    |
    v
[Quality Control] --> FastQC, MultiQC
    |
    v
[Trimming] --> Trimmomatic, fastp
    |
    v
[Alignment] --> STAR, HISAT2
    |
    v
[Quantification] --> featureCounts, Salmon
    |
    v
[Differential Expression] --> DESeq2, edgeR
    |
    v
[Pathway Analysis] --> clusterProfiler, GSEA

# Run FastQC on all FASTQ files
fastqc -t 8 -o qc_results/ raw_data/*.fastq.gz

# Aggregate QC reports
multiqc qc_results/ -o multiqc_report/

# fastp for quality trimming and adapter removal
fastp \
  --in1 sample_R1.fastq.gz \
  --in2 sample_R2.fastq.gz \
  --out1 trimmed_R1.fastq.gz \
  --out2 trimmed_R2.fastq.gz \
  --detect_adapter_for_pe \
  --thread 8 \
  --html fastp_report.html

# Build genome index (one time)
STAR --runMode genomeGenerate \
  --genomeDir star_index/ \
  --genomeFastaFiles genome.fa \
  --sjdbGTFfile annotations.gtf \
  --runThreadN 16

# Align reads
STAR --runMode alignReads \
  --genomeDir star_index/ \
  --readFilesIn trimmed_R1.fastq.gz trimmed_R2.fastq.gz \
  --readFilesCommand zcat \
  --outSAMtype BAM SortedByCoordinate \
  --quantMode GeneCounts \
  --outFileNamePrefix sample_ \
  --runThreadN 16

library(DESeq2)

# Load count matrix and sample info
counts <- read.csv("gene_counts.csv", row.names = 1)
coldata <- read.csv("sample_info.csv", row.names = 1)

# Create DESeq2 object
dds <- DESeqDataSetFromMatrix(
  countData = counts,
  colData = coldata,
  design = ~ condition
)

# Filter low-count genes
keep <- rowSums(counts(dds) >= 10) >= 3
dds <- dds[keep, ]

# Run differential expression
dds <- DESeq(dds)
res <- results(dds, contrast = c("condition", "treated", "control"),
               alpha = 0.05)

# Summary
summary(res)

# Export significant genes
sig_genes <- subset(as.data.frame(res), padj < 0.05 & abs(log2FoldChange) > 1)
write.csv(sig_genes, "significant_genes.csv")

Genotype Data (VCF/PLINK)
    |
    v
[Quality Control] --> Sample/variant filtering
    |
    v
[Population Stratification] --> PCA
    |
    v
[Association Testing] --> PLINK2, REGENIE
    |
    v
[Multiple Testing Correction] --> Bonferroni, FDR
    |
    v
[Visualization] --> Manhattan plot, QQ plot

# Sample QC
plink2 \
  --bfile dataset \
  --mind 0.05 \          # Remove samples with >5% missing
  --geno 0.02 \          # Remove variants with >2% missing
  --maf 0.01 \           # Remove rare variants (MAF < 1%)
  --hwe 1e-6 \           # HWE filter
  --make-bed \
  --out dataset_qc

# LD pruning for PCA
plink2 \
  --bfile dataset_qc \
  --indep-pairwise 50 5 0.2 \
  --out pruned

# PCA for population stratification
plink2 \
  --bfile dataset_qc \
  --extract pruned.prune.in \
  --pca 10 \
  --out pca_results

# Linear/logistic regression with covariates
plink2 \
  --bfile dataset_qc \
  --glm \
  --pheno phenotypes.txt \
  --covar pca_results.eigenvec \
  --covar-col-nums 3-12 \
  --out gwas_results

import pandas as pd
import matplotlib.pyplot as plt
import numpy as np

def manhattan_plot(gwas_file, output='manhattan.pdf'):
    df = pd.read_csv(gwas_file, sep='\t')
    df['-log10p'] = -np.log10(df['P'])

    # Assign cumulative positions
    df = df.sort_values(['CHR', 'BP'])
    df['pos_cum'] = 0
    offset = 0
    for chrom in df['CHR'].unique():
        mask = df['CHR'] == chrom
        df.loc[mask, 'pos_cum'] = df.loc[mask, 'BP'] + offset
        offset = df.loc[mask, 'pos_cum'].max()

    fig, ax = plt.subplots(figsize=(16, 5))
    colors = ['#3B82F6', '#94A3B8']
    for i, chrom in enumerate(df['CHR'].unique()):
        subset = df[df['CHR'] == chrom]
        ax.scatter(subset['pos_cum'], subset['-log10p'],
                   s=2, color=colors[i % 2], alpha=0.7)

    ax.axhline(-np.log10(5e-8), color='red', linestyle='--', linewidth=0.8)
    ax.set_xlabel('Chromosome')
    ax.set_ylabel('-log10(p-value)')
    fig.savefig(output, dpi=300, bbox_inches='tight')

# Mark duplicates
gatk MarkDuplicates \
  -I aligned.bam \
  -O dedup.bam \
  -M metrics.txt

# Base quality score recalibration
gatk BaseRecalibrator \
  -I dedup.bam \
  -R reference.fa \
  --known-sites dbsnp.vcf \
  -O recal_table.txt

gatk ApplyBQSR \
  -I dedup.bam \
  -R reference.fa \
  --bqsr-recal-file recal_table.txt \
  -O recal.bam

# Call variants
gatk HaplotypeCaller \
  -I recal.bam \
  -R reference.fa \
  -O variants.g.vcf \
  -ERC GVCF