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DSTC-A68 Online (e-LMS) Advanced Postgrad

Basics of SNPs and Genomic Variants

by - DSTC

Master Basics of SNPs and Genomic Variants in 4 weeks through hands-on, project-based online training with DSTC.

★★★★★ Be the first to review • 4 Weeks · 40 hrs • e-Certificate Included
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From ₹200 + GST

Programme Parameters

Educational Level:
Advanced Postgrad
Duration & Workload:
4 Weeks (40 Hrs)
Delivery Mode:
Online (e-LMS)
Prerequisites:
• Prior working knowledge of the field and comfort with core tools and quantitative reasoning.
• A laptop or desktop with a stable internet connection.
• Willingness to complete assignments and the capstone project.

About This Course

The Basics of SNPs and Genomic Variants course is a free, beginner-friendly self-paced program designed to introduce learners to the concepts of Single Nucleotide Polymorphisms (SNPs) and genomic variants, and how they impact genetic research, disease studies, and personalized medicine. Every participant receives a verified e-Certificate and e-Marksheet from the Deep Science & Technology Consortium.

🎯 Program Aim

The Basics of SNPs and Genomic Variants course is a free, beginner-friendly self-paced program designed to introduce learners to the concepts of Single Nucleotide Polymorphisms (SNPs) and genomic variants, and how they impact genetic research, disease studies, and personalized medicine.

📋 Course Objectives

1. Translate Artificial Intelligence theory into practical, reproducible analysis.
2. Build a defensible project you can showcase to supervisors, reviewers, or employers.

👥 Who Should Enroll?

• Master's and senior undergraduate students specializing in Artificial Intelligence
• R&D engineers and working professionals applying Artificial Intelligence in industry
• Academics and educators building research or teaching capacity in Artificial Intelligence

🚀 Key Learning Outcomes

• Tangible, reproducible Artificial Intelligence work to show supervisors or employers.
• A verified e-Certificate of competency and e-Marksheet from the Deep Science & Technology Consortium.

💎 What You'll Gain

🎥

Live & Recorded Sessions

Lifetime access to class recordings
🎓

e-Certificate on Completion

Cryptographically verified credential
💬

Post-Programme Support

Direct access to mentors & council
💻

Hands-On Experience

Notebooks, real-world code & datasets

Curriculum Outline

Module 1 Outline

Introduction to SNPs and Genomic Variants

What are SNPs (Single Nucleotide Polymorphisms)? • Types of Genomic Variants (SNPs, InDels, CNVs) • Role of Genetic Variants in Genomics • Applications in Medicine and Biotechnology

Module 2 Outline

Understanding Genomic Variants

Types of Genetic Variants: SNPs, Insertions, Deletions, and Structural Variants • How Variants Affect Genes and Proteins • Understanding Mutations and Their Impact on Health • Genetic Variation in Populations

Module 3 Outline

Identifying SNPs and Genomic Variants

Techniques for SNP Detection • Genomic Databases and Variant Repositories • Next-Generation Sequencing (NGS) and SNP Analysis • Tools for SNP Annotation and Interpretation

Module 4 Outline

Applications of SNPs and Genomic Variants

Genomic Variants in Disease Research (Cancer, Genetic Disorders, etc.) • SNPs in Personalized Medicine and Pharmacogenomics • Genetic Markers for Disease Susceptibility • Genomic Variants in Agriculture and Biotechnology

Module 5 Outline

Future Scope and Learning Path

Emerging Technologies in Variant Detection • Role of AI and Big Data in Genetic Studies • Career Opportunities in Genomics, Bioinformatics, and Medicine • Mini Learning Activity / Concept-Based Practice

Technical Specifications

ParameterRequirement
Covered Tool / PlatformSNPs (Single Nucleotide Polymorphisms)
Covered Tool / PlatformGenomic Variants
Covered Tool / PlatformGenomic Data
Covered Tool / PlatformMutation Detection
Covered Tool / PlatformNext-Generation Sequencing (NGS)

Frequently Asked Questions

Yes. This is a free online self-paced course designed for beginners.

No. The course focuses on biological concepts and does not require coding experience.

You will learn the basics of SNPs and genomic variants, their role in disease research, and the techniques used for identifying and analyzing genetic variations.

Students, beginners, biotechnology learners, healthcare professionals, and researchers interested in genetic research and genomic analysis can join.

Yes. Learners receive an e-Certification after completing the course.

SNPs (Single Nucleotide Polymorphisms) are variations in a single nucleotide that occur in the DNA sequence. These variations can have important effects on gene function and contribute to diseases.

Genetic variants include SNPs, insertions, deletions, and structural variations. These variations can affect genes and proteins, leading to various health outcomes.

NGS is a high-throughput method used to sequence DNA and RNA, which helps in identifying SNPs and other genetic variants across genomes.

Yes. This course is designed for non-technical learners who are interested in understanding SNPs, genomic variants, and their applications in health and biotechnology.

The course explains the fundamentals of SNPs and genomic variants in simple language and provides real-world examples, making it accessible for beginners without prior knowledge of genomics. The Basics of SNPs and Genomic Variants course provides a simple and structured foundation for understanding genetic variation and its implications in disease, medicine, and biotechnology. It is an ideal starting point for learners interested in genomics, genetic research, and personalized medicine.

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