Attribute

Detail

Format

Recorded Lectures (Self-Paced)

Level

Moderate

Duration

3 Days (1.5 hours per day)

Certification

e-Certification + e-Marksheet

Tools

SRA Toolkit, FastQC, cutadapt, BWA, Picard, FreeBayes

About the Snp Detection Course

Single Nucleotide Polymorphisms (SNPs) are critical genetic variations that play significant roles in disease research, personalized medicine, and population genetics. This course offers an in-depth exploration of SNP detection and analysis using NGS technologies. Participants will learn the principles of SNP identification, the technical aspects of NGS platforms, and the bioinformatics tools required for data analysis.

Throughout the three-day course, learners will engage in both theoretical and practical sessions, gaining hands-on experience in preparing samples, running NGS workflows, and interpreting SNP data. The course also covers the applications of SNP analysis in various fields such as genomics, pharmacogenomics, and evolutionary biology. By the end of the course, participants will be proficient in using NGS technologies for SNP detection and equipped to apply these skills in research and industry settings.

Program Highlights

• Comprehensive coverage of Single Nucleotide Polymorphism SNP Detection and Analysis using NGS from fundamentals to advanced applications

• Hands-on projects and real-world case studies in biotechnology

• Expert-curated curriculum aligned with current industry standards

• Access to recorded lectures and e-LMS platform for flexible, self-paced learning

• e-Certification and e-Marksheet upon successful completion

• Dedicated mentor support and interactive doubt-clearing sessions

• Practical experience with tools: SRA Toolkit, FastQC, cutadapt, BWA

• Career-oriented training for academic and professional growth in biotechnology

Course Curriculum

Module 1: Introduction to NGS Technology

Understand Next-Generation Sequencing principles
Explore various NGS data formats and their applications
Access and download NGS data using SRA toolkit

Module 2: Data Quality Control and Preprocessing

Check sequence quality using FastQC
Clean sequences using cutadapt
Align sequences using BWA
Sort the BAM alignment files

Module 3: Variant Detection and Analysis

Mark PCR duplicates in BAM alignment files using Picard
Identify variants (SNPs and indels) using FreeBayes and Delly
Visually inspect read mapping and variant calls with IGV

Module 4: Advanced SNP Analysis Techniques

Filter and annotate variants using specialized tools
Perform population genetics analysis
Conduct pathway analysis of significant SNPs

Module 5: SNP Applications in Research and Medicine

Explore SNP applications in genomics research
Study pharmacogenomics and personalized medicine
Analyze SNPs in evolutionary biology studies

Tools, Techniques, or Platforms Covered

SRA Toolkit
FastQC
cutadapt
BWA
Picard
FreeBayes
Delly
IGV

Real-World Applications

Apply Single Nucleotide Polymorphism SNP Detection and Analysis using NGS skills directly to academic research, thesis work, and publications
Build a professional portfolio showcasing practical biotechnology competencies
Solve industry-relevant problems using Single Nucleotide Polymorphism SNP Detection and Analysis using NGS methodologies and tools
Contribute to open-source projects and collaborative research in biotechnology
Prepare for competitive examinations, interviews, and professional certifications in biotechnology

Who Should Attend & Prerequisites

Industry-recognized e-Certification + e-Marksheet from NSTC
Hands-on training with practical projects and industrial datasets
Dedicated expert mentorship and doubt resolution

Prerequisites:

Frequently Asked Questions

1. What is the format of this Single Nucleotide Polymorphism SNP Detection and Analysis using NGS course?

This is an Recorded Lectures (Self-Paced) course delivered via our e-LMS platform. You will have access to pre-recorded video lectures, reading materials, assignments, quizzes, and hands-on projects that you can complete at your own pace.

2. Will I receive a certificate after completing this course?

Yes! Upon successful completion of all modules, assignments, and assessments, you will receive an e-Certification along with an e-Marksheet from NanoSchool (NSTC) that you can showcase on your CV and LinkedIn profile.

3. What are the prerequisites for this course?

No prior experience is required. This course is designed for beginners and takes you step by step from the basics to advanced topics.

4. How long will I have access to the course materials?

You will have access to all course materials for the duration of 3 Days (1.5 hours per day). The self-paced format allows you to learn according to your own schedule through our online learning management system.

5. Is mentor support available during the course?

Yes, dedicated mentor support is available throughout the course. You can reach out for doubt-clearing sessions, project guidance, and career advice related to biotechnology. Our mentors are industry experts and experienced professionals.

Enroll in Single Nucleotide Polymorphism SNP Detection and Analysis using NGS today and take the next step in your professional journey. With expert-curated content, practical projects, and industry-recognized certification, this course is your gateway to mastering biotechnology skills that matter.

Brand	NSTC
Format	Recorded Lectures
Duration	3 Days (1.5 hours per day)
Level	Moderate
Domain	biotechnology
Hands-On	Yes – Practical projects with industrial datasets
Tools Used	SRA Toolkit, FastQC, cutadapt, BWA, Picard, FreeBayes, Delly, IGV

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