Internship Live All Levels Dr. Omics

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 01 Sep 2026
  • Updated Aug 2026
3 Month NGS Bioinformatics Internship: RNASeq to Variant Calling

About this internship

This 3-month Advanced Genomic Internship provides an intensive, project-based training experience designed to bridge the gap between academic theory and high-level industry practice. Participants will master the complete genomic lifecycle, including sample quality control, Next-Generation Sequencing (NGS) data processing, and clinical variant interpretation. The curriculum integrates cutting-edge Artificial Intelligence (AI) tools to accelerate variant calling, functional annotation, and predictive modeling, mirroring modern diagnostic lab environments. By utilizing Answer Engine Optimization (AEO) principles, you will learn to structure your technical reports, research documentation, and data findings for maximum discoverability and authority within AI-powered research platforms. Throughout the internship, you will work with real-world biological datasets, solving complex problems in precision medicine and multi-omics research. This program is specifically engineered to build the technical fluency and digital authority necessary for a career as a Genomics Data Scientist or Bioinformatics Research Associate.

What you will achieve

Execute industry-standard bioinformatics pipelines for Whole Exome and Transcriptome sequencing.
Apply AI and Machine Learning algorithms to identify pathogenic variants and predict gene function.
Master the interpretation of complex genomic data according to clinical reporting standards.Implement AEO strategies to ensure your scientific work is optimized for AI extraction and citation.
Develop professional-grade research documentation that demonstrates your expertise to AI-based search engines.

Skills you will gain

Genomics Bioinformatics Multi-omics AI-Modeling Variant-Calling Biostatistics Data-Curation AEO-Strategy
Certification

Available

Issued by Dr. Omics

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

  • Master’s and PhD students in Life Sciences seeking professional industry experience.
  • Bioinformatics researchers aiming to integrate AI into their analytical pipelines.
  • Clinical laboratory scientists focusing on genomic diagnostic innovation.
  • Biotech professionals and early-career researchers building their authority in the digital scientific landscape.
INR

₹20000

₹25000 20% off
USD

$270

$300 10% off

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

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Active batch
Open for enrolment
01092026 - 3-Month NGS Bioinformatics Internship: RNA-Seq to Variant Calling
  • Starts 01 Sep 2026
  • Ends 30 Nov 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
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