A 2-day hands-on workshop. From raw FASTQ files to a fully interpreted DGE analysis — using real clinical datasets. Take your results home and straight into your thesis.
Seats are limited to 30
Early-bird pricing ends when seats fill
All tiers include 2 days of training, lunch, course materials, and a certificate. GST invoice provided.
GST invoice issued on request · Group discounts available for 3+ registrations from the same institution
Every session is hands-on at the terminal. No slide-deck-only lectures. You run every command on real clinical RNA-seq datasets.
Terminal basics, FastQC, Trimmomatic, HISAT2 alignment, SAMtools. Getting from raw reads to sorted BAM.
featureCounts / HTSeq, understanding count matrices, normalisation concepts, preparing your data for DGE.
Setting up DESeq2 in R, running DGE, interpreting padj values, handling NA results, volcano plots.
Gene Ontology analysis with clusterProfiler, KEGG pathway enrichment, heatmaps, publication-ready figures.
Prerequisites
No prior bioinformatics experience required. Basic computer skills sufficient. A laptop with at least 8GB RAM is mandatory — installation guide sent on registration.
What's included
Fill in the form and we'll confirm your seat and send payment details within 24 hours. Batch is limited to 30 participants.
📅 19–20 September 2026
Ahmedabad, Gujarat · Venue details sent on registration confirmation
We'll confirm your seat and send payment details within 24 hours. GST invoice provided.