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BIO HELP LEARNING COURSE

ATAC-Seq Data Analysis Training

★★★★★4.8/5(200+ reviews)
◉ Beginner to Advanced◷ 15 Hours / Live▣ Yes — Certificate of Completion

About This Course

What You’ll Learn

Understand the principles and applications of ATAC-Seq
Understand chromatin accessibility and regulatory genomics
Perform quality assessment of ATAC-Seq sequencing data
Perform read preprocessing and genome alignment
Process and evaluate ATAC-Seq BAM files
Perform peak calling to identify accessible chromatin regions
Analyze genomic distribution of ATAC-Seq peaks
Perform transcription factor motif analysis
Visualize accessibility signals using genome browsers
Interpret ATAC-Seq results in a biological context

Tools & Technologies

FastQCBowtie2SamtoolsMACS3deepToolsIGVHOMER

Course Curriculum

15 Modules

Your Instructor

Bio Help Learning Educator

Bio Help Learning Educator

Educator | Mentor

Learn from experienced educators and practitioners through practical, career-focused bioinformatics training.

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Student Reviews

★★★★★ 4.8/5 (200+ reviews)
AV

“Excellent course! The content is practical and the projects made the concepts much easier to apply.”

Ananya VermaPhD Scholar, India★★★★★
RM

“Hands-on projects made all the difference. Highly recommended for anyone interested in NGS.”

Rahul MehtaResearch Associate, Germany★★★★★
SM

“Very detailed and industry-relevant content. I feel much more confident now.”

Sneha PatelBioinformatics Analyst, India★★★★★
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Frequently Asked Questions

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What is ATAC-Seq?

ATAC-Seq is a sequencing-based method used to identify regions of open or accessible chromatin across the genome.

Who can join this ATAC-Seq training?

The course is suitable for biotechnology, bioinformatics, life science, genetics, genomics and related students, researchers and professionals.

Do I need prior ATAC-Seq experience?

No. The course begins with fundamental concepts and progressively moves toward practical data analysis.

Will this course include hands-on analysis?

Yes. The training focuses on practical ATAC-Seq analysis using sequencing datasets.

Which tools will I learn?

You will work with FastQC, Bowtie2, Samtools, MACS3, deepTools, IGV and HOMER.

Will I learn peak calling?

Yes. You will learn to identify accessible chromatin regions using peak-calling workflows.

Will I learn motif analysis?

Yes. The curriculum includes motif discovery and transcription factor analysis.

Will I learn differential accessibility analysis?

Yes. The course introduces comparison of chromatin accessibility between experimental conditions.

Will I receive a certificate?

Yes, participants can receive a certificate upon successful completion of the training.

Is there a project at the end of the course?

Yes. Day 15 includes a mini project covering the complete ATAC-Seq data analysis workflow.

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