Learn Single-Cell RNA-Seq Data Analysis Using R & Python

Master Single-Cell RNA-seq Analysis from Scratch Using R, Python, and Cloud Tools — Master QC, Clustering and Annotation

Learn Single-Cell RNA-Seq Data Analysis Using R & Python

Learn Single-Cell RNA-Seq Data Analysis Using R & Python udemy course free download

Master Single-Cell RNA-seq Analysis from Scratch Using R, Python, and Cloud Tools — Master QC, Clustering and Annotation

Welcome to our comprehensive course, “Learn Single-Cell RNA-Seq Data Analysis Using R, Python, GUI Tools, and Cloud Platforms,” designed to empower you with the essential skills and knowledge to explore one of the most advanced and high-resolution technologies in genomics: Single-Cell RNA Sequencing (scRNA-seq).

In the era of precision biology, where understanding individual cellular behavior is critical to unlocking insights in cancer biology, immunology, neuroscience, and regenerative medicine, scRNA-seq has emerged as a transformative tool. This course serves as your complete entry point into the field of single-cell transcriptomics, guiding you from foundational theory to hands-on data analysis using the most powerful open-source tools available.

Why Single-Cell RNA-Seq?

With the limitations of traditional bulk RNA sequencing—where gene expression is averaged across thousands or millions of cells—scRNA-seq allows you to analyze gene expression at single-cell resolution, revealing the hidden heterogeneity in tissues, uncovering rare cell types, and providing new dimensions to disease understanding and treatment strategies.

Bioinformatics for the Single Cell Era

At the heart of this course is the interdisciplinary power of bioinformatics—a fusion of biology, computer science, and data science. You’ll master the computational approaches and statistical frameworks that drive modern single-cell data analysis, learning how to interpret, visualize, and extract meaningful biological insights from complex datasets.

Comprehensive Learning Journey: From the basics of single-cell technology to full-scale analysis workflows, this course walks you through every step of scRNA-seq data analysis with clarity and practical insight.

Multi-Tool Mastery: You'll gain hands-on experience with both R and Python-based analysis pipelines, using powerful libraries like Seurat and Scanpy, while also exploring graphical interfaces and cloud-based platforms like Galaxy for non-coders.

Real-World Data: Work with real scRNA-seq datasets from public repositories like NCBI GEO, giving you confidence in applying your skills to actual biological data.

Expert Instruction: Learn from experienced bioinformatics educators who break down complex concepts into manageable, actionable learning steps.
Section 1: Introduction to Single-Cell RNA-Seq

  • What is scRNA-seq and how it differs from bulk RNA-seq

  • Real-world applications in medicine and biology

  • A clear overview of the entire analysis pipeline

Section 2: Getting Started with R and RStudio

  • Introduction to R programming for biologists

  • Installing RStudio and understanding data structures

  • Importing data, managing packages, and creating visualizations using ggplot2 and Seurat

Section 3: Single-Cell RNA-Seq Analysis in R

  • Preprocessing scRNA-seq data with Seurat

  • Quality control, normalization, scaling, and PCA

  • Clustering, UMAP visualization, marker gene identification, and cell type annotation

Section 4: Single-Cell RNA-Seq Analysis in Python

  • Using Scanpy and scVI-tools

  • Replicating full pipelines in Python

  • Advanced annotation using models like scANVI

Section 5: GUI and Cloud-Based Pipelines

  • Running scRNA-seq analysis without coding

  • Using platforms like Galaxy, CodeOcean, or Cellxgene

  • Downloading and analyzing GEO datasets visually

Who This Course Is For:

  • Biology or medical students transitioning into bioinformatics

  • Bioinformatics beginners and researchers

  • Data scientists exploring single-cell applications

  • Wet lab scientists wanting to analyze their own scRNA-seq data

  • Anyone interested in high-resolution transcriptomics

What You Need:

  • No prior coding experience required — this course is beginner-friendly

  • All tools used are open-source and freely available

  • Basic familiarity with biology or interest in genomics is helpful

Join us in this immersive learning experience and gain the confidence to run full single-cell RNA-seq analysis pipelines, interpret your results, and contribute meaningfully to cutting-edge research. Whether you aim to build a research career or enhance your skill set as a life science professional, this course is your gateway to mastering single-cell bioinformatics using R, Python, GUI tools, and cloud platforms.