As a bioinformatician, the most common request I receive is to analyze sequencing data. I prepared this seminar focused on the recommendations I would love to have when I’ve started on this path.
Whether you’re working with private or public data, here’s the workflow I always recommend:
✅ Set up a clean project folder from day one
✅ Estimate your file sizes and check storage & compute capacity
✅ Retrieve your raw data (private or public sources)
✅ Run QC — non-negotiable
✅ Launch your NGS pipeline of choice
💡 Pro tip: always run the full pipeline on a single sample first to benchmark time and resources.
If you’re not sure where to begin, let’s talk. Book a free 30-minute call and we’ll design a plan tailored to your data and goals.
🔗 https://instats.org/seminar/rna-seq-from-fastq-to-counts-1
📩 DM me for a personal discount on the seminar
contact@estepi.com
