NGS Data Analysis Training

NGS data analysis training — read processing, quality control, alignment, variant calling, and downstream interpretation across DNA and RNA workflows.

What is NGS Data Analysis Training?

This programme is for students who need real, hands-on competence with NGS pipelines. You take raw FASTQ data through a complete analysis — QC, alignment, variant calling or expression analysis, and biological interpretation.

What you will learn

FASTQ format, sequencing chemistries, and read-quality fundamentals
Quality control (FastQC, MultiQC) and adapter trimming (Trim Galore, fastp)
Alignment with BWA, Bowtie2, HISAT2, STAR — choosing the right tool
Variant calling (GATK / bcftools) with annotation using SnpEff or VEP
RNA-seq quantification and DE analysis (DESeq2 / edgeR)
Reproducibility — Conda environments, basic scripting, version tracking

Who this is for

Students from bioinformatics, biotechnology, genetics, molecular biology, and computational biology. A working comfort with the command line is helpful; we calibrate to your starting level.

What you take away

NTHRYS training certificate detailing NGS scope
A reproducible end-to-end pipeline on a real dataset
Hands-on experience with the tools genomics employers actually use
A direct lift into bioinformatics, genomics, and clinical-genomics roles

Pick the field below to see specific NGS analysis training options.

Pick your field of interest

Loading fields…

Prefer to chat first? Talk to our coordinators directly