Unlock the power of genomic data. Master NGS pipelines, variant calling, and multi-omics integration for deep biological discovery and clinical precision.
Modular online course with applied concepts + mentor-led workshops
Intermediate
8 weeks
Conceptual + computational + analytical application
FastQC, BWA, GATK, Samtools, IGV, DESeq2
NGS pipeline execution, variant calling, RNA-seq analysis
Genomics, Bioinformatics, NGS Analysis, Multi-Omics
NGS technology, platforms, and data formats. Overview of end-to-end pipeline stages from raw reads to insights.
Quality control metrics, trimming, and filtering. Ensuring data integrity before downstream analysis.
Sequence alignment algorithms and tools. Mapping reads to reference genomes and post-alignment QC.
SNP and indel detection using GATK and Samtools. Variant filtering and functional annotation.
Transcriptome analysis, differential expression with DESeq2, and transcript quantification.
Functional annotation, clinical relevance, and variant prioritization for research and diagnostics.
Integrating genomics with transcriptomics. Systems biology approaches to cross-omics interpretation.
End-to-end NGS analysis and multi-omics integration project. Final portfolio presentation.
| Category | Launch Offer (INR) | Regular Price (INR) | International (USD) |
|---|---|---|---|
| Student | ₹9,999 | ₹14,999 | $350 |
| PhD / Researcher | ₹12,999 | ₹18,999 | $450 |
| Faculty | ₹13,999 | ₹21,999 | $500 |
| Industry Professional | ₹14,999 | ₹24,999 | $600 |
Become an industry-ready bioinformatics leader with real NGS pipeline skills.
