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NGS and Transcriptomic Data Analysis: From Raw Reads to Biological Insights
Original price was: USD $99.00.USD $59.00Current price is: USD $59.00.
An on‑demand, recorded course that teaches you how to perform end‑to‑end NGS and transcriptomic data analysis—from raw sequencing reads through quality control, alignment/quantification, normalization, differential expression testing, and biological interpretation—so you can turn complex sequence data into meaningful insights.
NGS & Transcriptomic Data Analysis: From Raw Reads to Biological Insights
Recorded on‑demand course • Practical NGS workflow • RNA‑Seq data interpretation
Instant Access
Beginner to Intermediate
QC → Alignment → DEA → Interpretation
Beginner to Intermediate
QC → Alignment → DEA → Interpretation
This recording‑based course equips you with the complete computational workflow for **next‑generation sequencing (NGS)** and **RNA‑Seq transcriptomic data analysis**. From raw sequencing outputs to actionable insights, learn how to control data quality, build clean count matrices, perform differential expression testing, and derive biological meaning from your results. :contentReference[oaicite:1]{index=1}
What You’ll Learn
- Key NGS and RNA‑Seq data concepts, formats, and experiment design
- Raw read quality control and trimming strategies
- Alignment or pseudo‑alignment and expression quantification
- Differential expression analysis and statistical interpretation
- Biological interpretation using pathway and enrichment analyses
- Publication‑ready visualization (QC reports, heatmaps, volcano plots)
Course Modules (Recordings)
Module 1 — NGS & RNA‑Seq Fundamentals
Understand sequencing data formats, experimental design fundamentals, and initial quality assessment of raw reads.
Module 2 — QC, Trimming, Alignment & Quantification
Learn how to control data quality, trim reads, and generate gene/transcript expression counts using trusted bioinformatics tools.
Module 3 — Differential Expression & Insights
Master differential expression workflows, interpret statistical results, and connect gene-level changes to biological pathways and functional mechanisms.
Tools Covered
FastQC, MultiQC, trimming tools (fastp/Trimmomatic), alignment/pseudo‑alignment tools, count generators, DEA tools, visualization libraries.
Who It’s For
Ideal for researchers, PhD scholars, postdocs, faculty, industry scientists, and postgraduate students who want job‑ready NGS and transcriptomic analysis skills.
What You’ll Get
- On‑demand access to all recording modules
- Practical workflows you can reuse on your own data
- Certificate of completion (if included in product package)
Tip: Use the recordings alongside your own datasets—pause, replay, and apply each step in real scenarios.
Note: This is an on‑demand (recording‑based) learning product. Access and deliverables depend on the product package settings.
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