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Single Nucleotide Polymorphism (SNP) Detection and Analysis using NGS
Uncover Genetic Variations with Precision: Master SNP Detection and Analysis using NGS
Online/ e-LMS
Self Paced
Moderate
1 Month
About
Single Nucleotide Polymorphisms (SNPs) are critical genetic variations that play significant roles in disease research, personalized medicine, and population genetics. This program 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 one-month program, 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 program, participants will be proficient in using NGS technologies for SNP detection and equipped to apply these skills in research and industry settings.
Aim
The aim of the “Single Nucleotide Polymorphism (SNP) Detection and Analysis using NGS” program is to equip participants with the knowledge and skills to detect and analyze SNPs using next-generation sequencing (NGS) technologies. This program will provide a thorough understanding of the workflows, tools, and techniques essential for SNP analysis in various biological and medical research applications.
Program Objectives
- Understand the principles and techniques of SNP detection using NGS.
- Gain proficiency in NGS workflows and data analysis for SNP identification.
- Explore the applications of SNP analysis in various fields of research.
- Develop skills in bioinformatics tools and software for genetic data analysis.
- Learn to interpret and apply SNP data in real-world scenarios.
Program Structure
Module 1
- Introduction to NGS Technology
- Overview of NGS data formats
- Accessing NGS data using SRA tool kit
Module 2
- Checking sequence quality using FastQC
- Cleaning the sequences using cutadapt
- Aligning sequences using BWA
- Sorting the BAM alignment files
Module 3
- Mark PCR duplicates in BAM alignment files using Picard
- Use FreeBayes and Delly on the BAM files to identify variants (SNPs and indels)
- Visually inspect read mapping and variant calls with the Integrated Genomics Viewer (IGV)
Note: Linux OS is required for running the tools
Participant’s Eligibility
- Undergraduate degree in Genetics, Bioinformatics, Biotechnology, or related fields.
- Professionals in the genomics, biotechnology, or pharmaceutical industries.
- Researchers and scientists with a keen interest in genetic variation and personalized medicine.
Program Outcomes
- Mastery of SNP detection and analysis using NGS technologies.
- Ability to run NGS workflows and interpret sequencing data.
- In-depth understanding of the applications of SNP analysis.
- Proficiency in using bioinformatics tools for genetic data analysis.
- Preparedness for careers in genomics, bioinformatics, and genetic research.
Fee Structure
Standard Fee: INR 4,998 USD 110
Discounted Fee: INR 2499 USD 55
We are excited to announce that we now accept payments in over 20 global currencies, in addition to USD. Check out our list to see if your preferred currency is supported. Enjoy the convenience and flexibility of paying in your local currency!
List of CurrenciesBatches
Certificate
Program Assessment
Certification to this program will be based on the evaluation of following assignment (s)/ examinations:
| Exam | Weightage |
|---|---|
| Mid Term Assignments | 50 % |
| Project Report Submission (Includes Mandatory Paper Publication) | 50 % |
To study the printed/online course material, submit and clear, the mid term assignments, project work/research study (in completion of project work/research study, a final report must be submitted) and the online examination, you are allotted a 1-month period. You will be awarded a certificate, only after successful completion/ and clearance of all the aforesaid assignment(s) and examinations.
Program Deliverables
- Access to e-LMS
- Real Time Project for Dissertation
- Project Guidance
- Paper Publication Opportunity
- Self Assessment
- Final Examination
- e-Certification
- e-Marksheet
Future Career Prospects
- Genomic Data Analyst
- Bioinformatics Scientist
- Genetic Counselor
- Clinical Genomics Specialist
- Pharmacogenomics Researcher
- Population Geneticist
Current Participants* Analytics
Country
Profession
Affiliation
Note: The information shown in the above-mentioned analytics is live and may include information that is not completely correct like spelling mistakes, grammatical mistakes , factual errors or even mis representation as this is what participants have entered, the information is currently not edited and or filtered , but at later stages they will be filtered to provide true data representation.
Enter the Hall of Fame!
Take your research to the next level!
Achieve excellence and solidify your reputation among the elite!
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Recent Feedbacks In Other Workshops
The course was more theoretical than practical.
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