Internship Live All Levels Dr. Omics Edu

3 Month NGS Bioinformatics Internship: RNASeq to Variant Calling

Master end-to-end genomic data analysis, AI-driven bioinformatics, and precision medicine workflows in this comprehensive 3-month research internship.

  • 5.0/5
  • English
  • Starts 15 Sep 2026
  • Updated Oct 2026
INR

₹25000

₹30000 17% off
USD

$270

$350 23% off

Indian learners pay in INR; international learners are billed in USD.

Enroll for International Students

Paying from outside India? Use this link to complete your payment.

3 Month NGS Bioinformatics Internship: RNASeq to Variant Calling

About this internship

The 3 Month NGS Bioinformatics Internship: RNASeq to Variant Calling at Dr. Omics Edu is a 3-month live, mentor-supervised internship in next generation sequencing (NGS) and genomics under NEP 2020. It covers both major NGS analysis routes, transcriptomics and variant discovery, across eight modules. You work on a real dataset and a defined research question, and you finish with a genomics or transcriptomics project from raw reads to interpreted results that you can show to an admissions panel, a guide or an employer.
In this internship you move through linux and command-line workflows for ngs, quality control and trimming of fastq reads and rna-seq alignment, quantification and differential expression, then apply them in your own project. The programme runs live online with 8 modules, so you can ask your mentor questions as you work. It is open to learners at every level, and mentors adjust the pace to your background.

What you will achieve

Linux and command-line workflows for NGS
Quality control and trimming of FASTQ reads
RNA-seq alignment, quantification and differential expression
Variant calling from DNA sequencing data
Variant annotation and filtering
A complete NGS project from raw reads to results
For careers: Bioinformatics analyst, genomics data analyst, NGS data scientist, research associate, and a stronger profile for M.Sc, MS or PhD admissions in genomics.

Skills you will gain

Linux FastQC Trimmomatic HISAT2/STAR SAMtools GATK DESeq2 R
Certification

Available

Issued by Dr. Omics Edu

Internship curriculum

8 modules

  • Lesson 1: Introduction
  • Lesson 2: Getting Started
  • Lesson 3: Basic Concepts

  • M1T1 = Introduction to Bioinformatics
  • M1T2 = NCBI Database Overview
  • M1T3 = Genbank Database Practical Exercises
  • M1T4 = UCSC Genome Browser Overview
  • M1T5 = UCSC Genome Browser Hands-on Exercises
  • M1T6 = Pubmed Database Introduction
  • M1T7 = Clinvar Database Overview
  • M1T8 = KEGG Database Overview and Exercises
  • M1T9 = Protein Databases (UniProt)
  • M1T10 = Protein Databases (PDB)
  • M1T11 = Online BLAST Introduction and Exercises
  • M1T12 = Standalone BLAST Setup and Exercises
  • M1T13 = Standalone BLAST Advanced Exercises
  • M1T14 = Multiple Sequence Alignment with ClustalW
  • M1T15 = Multiple Sequence Alignment with MEGA

  • M2T1 = Overview and Installation of Linux
  • M2T2 = Basic Linux Commands
  • M2T3 = Advanced Linux Commands
  • M2T4 = Package Management using Repository
  • M2T5 = Package Management using Source Code

  • M3T1 = Introduction to Python
  • M3T2= Data Types
  • M3T3= String Handling
  • M3T4= Data Structure
  • M3T5=Control Structure
  • M3T6 = Function
  • M3T7= File Handling
  • M3T8= Data Manipulation
  • M3T9= Data Visualization
  • M3T10= Biopython

  • M4T1 = Introduction and Installation of R
  • M4T2= Data Types in R
  • M4T3= Data Structure
  • M4T4= File Handling
  • M4T5=Control Structure
  • M4T6 = Function
  • M4T7= Package Management
  • M4T8= Data Manipulation
  • M4T9= Data Visualization
  • M4T10= Statistical Analysis

  • HR Sessions

  • M6T1= Introduction to NGS and DNAseq
  • M6T2= Basic Terminologies in NGS
  • M6T3= Understanding of SRA database
  • M6T4= Tools installation in Linux for Variation Calling
  • M6T5= Quality control
  • M6T6= Trimming of Reads
  • M6T7= Indexing of Genome and Alignment of Reads
  • M6T8= Variation calling using GATK
  • M6T9= Variant Effect Prediction(VEP)
  • M6T10= Variation Visualization (IGV)

  • Project on NGS- DNA Seq Data Analysis

What you need to start

  • Foundational knowledge of Molecular Biology and Genetics.
  • Basic familiarity with programming (R or Python) and command-line environments.
  • A strong analytical mindset and a commitment to completing a rigorous 3-month research project.

Who this internship is for

  • B.Sc, M.Sc, B.Tech, M.Tech and PhD students in biotechnology, genetics, microbiology, biochemistry, life sciences or bioinformatics, plus early-career researchers.
INR

₹25000

₹30000 17% off
USD

$270

$350 23% off

Indian learners pay in INR; international learners are billed in USD.

Enroll for International Students

Paying from outside India? Use this link to complete your payment.

Active batch
Open for enrolment
01092026 - 3-Month NGS Bioinformatics Internship: RNA-Seq to Variant Calling
  • Starts 15 Sep 2026
  • Ends 15 Dec 2026
  • Timing 7:00 PM – 8:00 PM
  • Days Mon, Tue, Wed, Thu, Fri
  • Platform MS Teams
This internship includes
  • Format Live
  • Level All Levels
  • Language English
  • Modules 8
  • Live project No
  • Certificate Yes
  • Provider Dr. Omics Edu
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