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Bioinformatics Methods for Transcriptomics

Master RNA sequencing analysis with hands-on training in tools like STAR, DESeq2, and IsoQuant. Ideal for intermediate bioinformaticians.

Master RNA sequencing analysis with hands-on training in tools like STAR, DESeq2, and IsoQuant. Ideal for intermediate bioinformaticians.

This course offers comprehensive training in bioinformatics methods for analyzing transcriptomic RNA sequencing data. Covering both short read (RNA-seq) and long read (PacBio, ONT) sequencing, it addresses core transcriptomics questions: gene and transcript expression, expression levels, and differences in gene expression and splicing patterns between conditions. Students gain hands-on experience with popular tools such as STAR, PsiCLASS, DESeq2, rMATS, MntJULiP, Minimap2, and IsoQuant. The course is structured into four modules, progressing from gene expression analysis to alternative splicing analysis, transcriptome reconstruction with long reads, and differential expression and splicing analysis. Designed for intermediate-level learners, it assumes basic knowledge of command-line bioinformatics tools in a Unix-type environment.

Instructors:

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Bioinformatics Methods for Transcriptomics

This course includes

17 Hours

Of Self-paced video lessons

Intermediate Level

Completion Certificate

awarded on course completion

2,435

What you'll learn

  • Perform gene expression analysis of RNA-seq data using tools like STAR and DESeq2

  • Conduct alternative splicing analysis with rMATS and MntJULiP

  • Reconstruct transcriptomes using long RNA sequencing reads with FLAIR and IsoQuant

  • Carry out differential expression and splicing analysis with long RNA sequencing data

  • Visualize transcriptomic data using tools like IGV and Jutils

  • Apply bioinformatics methods to real-world transcriptomics datasets

Skills you'll gain

bioinformatics
RNA-seq
transcriptomics
gene expression
alternative splicing
STAR
DESeq2
rMATS
IsoQuant

This course includes:

7.85 Hours PreRecorded video

8 assignments

Access on Mobile, Tablet, Desktop

FullTime access

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There are 4 modules in this course

This course provides a comprehensive exploration of bioinformatics methods for analyzing transcriptomic RNA sequencing data. It covers both short read (RNA-seq) and long read (PacBio, ONT) sequencing technologies. The curriculum is designed to address core transcriptomics questions, including gene and transcript expression identification, expression level quantification, and analysis of differential gene expression and splicing patterns between experimental conditions. Students will gain practical experience using popular bioinformatics tools such as STAR, PsiCLASS, DESeq2, rMATS, MntJULiP, Minimap2, and IsoQuant. The course structure progresses from fundamental gene expression analysis to advanced topics like alternative splicing analysis and transcriptome reconstruction using long reads. This intermediate-level course assumes basic familiarity with command-line bioinformatics tools in a Unix environment, making it ideal for researchers and professionals looking to enhance their skills in transcriptomics data analysis.

Course Introduction and Gene expression analysis of RNA-seq data

Module 1 · 4 Hours to complete

Alternative splicing analysis of RNA-seq data

Module 2 · 4 Hours to complete

Transcriptome reconstruction with long RNA sequencing reads

Module 3 · 4 Hours to complete

Differential expression and differential splicing analysis with long RNA sequencing reads

Module 4 · 4 Hours to complete

Fee Structure

Payment options

Financial Aid

Instructor

Liliana Florea
Liliana Florea

29,730 Students

2 Courses

Associate Professor of Medicine at Johns Hopkins University

Dr. Liliana Florea is an Associate Professor of Medicine in the McKusick-Nathans Department of Genetic Medicine at Johns Hopkins University, where she specializes in developing computational methods for analyzing large-scale sequencing data to better understand the molecular mechanisms of diseases. Her research focuses on genome comparison, gene characterization, alternative splicing variations, and identifying genetic and molecular determinants of disease. Before joining Johns Hopkins in 2011, Dr. Florea was on the faculty at George Washington University and was a key member of the team at Celera Genomics that produced the first human genome sequence. Her work has earned her a Sloan Research Fellowship in Computational and Evolutionary Molecular Biology, with funding from the National Science Foundation and National Institutes of Health. She holds a PhD from Pennsylvania State University.

Bioinformatics Methods for Transcriptomics

This course includes

17 Hours

Of Self-paced video lessons

Intermediate Level

Completion Certificate

awarded on course completion

2,435

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