Bulk Rna-seq Analysis
Bioinformatics pipeline for Illumina human exome variant calling using FastQC, Trimmomatic, BWA, Samtools, Bcftools, and SnpEff. Demonstrates a reproducible workflow for NGS data analysis. #bioinformatics #genomics #variant-calling #ngs #pipeline
Genomic Analysis Pipeline: Automate data preprocessing, variant calling, and annotation with Snakemake. Ensure reproducibility and reliability in genomic studies.
Variantes genéticas de amostras de Rattus norvegicus utilizando GATK4
Detecting contamination in NGS data and multi-species analysis
Add a description, image, and links to the bwa topic page so that developers can more easily learn about it.
To associate your repository with the bwa topic, visit your repo's landing page and select "manage topics."