NGS Data Analysis Workshop

NGS data analysis workshop — read processing, QC, alignment, variant calling, and downstream interpretation across DNA / RNA workflows in a focused workshop format.

What is the NGS Data Analysis Workshop?

This workshop takes raw NGS data through a complete analysis pipeline — QC, alignment, variant calling or RNA-seq quantification, and biological interpretation. Compact format, real datasets, real outputs.

What you will do

Inspect FASTQ files and run quality control with FastQC and MultiQC
Trim adapters and low-quality bases with fastp / Trim Galore
Align reads using BWA, Bowtie2, HISAT2, or STAR
Call variants with GATK / bcftools and annotate with SnpEff or VEP
Run RNA-seq quantification and DE analysis with DESeq2
Document a reproducible, version-controlled mini-pipeline

Who this is for

Students and researchers from bioinformatics, biotechnology, genetics, molecular biology, and computational biology. Some command-line comfort helps; we calibrate to your starting level.

What you take away

NTHRYS workshop completion certificate
A reproducible end-to-end NGS pipeline on a real dataset
Hands-on experience with industry-standard NGS tools
A direct lift into bioinformatics, genomics, and clinical-genomics roles

Pick the field below to see specific NGS workshop options.

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