Build the computational skills that real bioinformatics careers demand — from day one.
Whether you're starting from scratch or already have data to analyze, there's a path designed for you.
Biology and life sciences students who want to add real computational skills before graduation.
PhD students tackling omics datasets as part of their thesis work — need depth and reproducibility.
Working researchers who generate data and need analysis skills to make sense of their results.
Biologists entering bioinformatics or computational biology roles and need a structured learning path.
The Core Track builds comprehensive skills from scratch. The Express Track gets researchers to results fast.
Five progressive tiers — join at your level, progress at your pace
DNA, RNA, Protein · Transcription & translation · Why computation in biology?
Major sequence, structure, and annotation databases · Searching and retrieving biological data.
Sequence files, alignment files, annotation files, variant files · What each represents and when to use it.
Local vs global alignment concepts · Scoring matrices · Hands-on similarity search · Tool landscape overview.
Retrieve a gene sequence from a public database, perform a similarity search, and interpret the results.
Variables, data types, loops, conditionals · Functions & modules · Reading/writing files · Biological context throughout.
R syntax & data structures · Data frames & basic manipulation · Plotting fundamentals · Biological context throughout.
Parsing sequence files, tabular omics data · Visualization of biological data · Choosing the right language for the right task.
Parse a biological sequence file, compute a sequence property of interest, and produce a clean visualization — implemented in both Python and R.
File system navigation · Permissions & ownership · Essential commands for biological file handling.
Stream editors and text processors for biological data · Parsing sequence, annotation, and alignment files · Piping & regular expressions.
Writing shell scripts · Loops & conditionals · Automating repetitive bioinformatics tasks · Variables & functions.
What is HPC and why it matters · Job scheduler concepts and submission · Managing large compute jobs · Software environment management.
Build an automated shell pipeline that processes multiple raw sequencing files — quality assessment, preprocessing, and summary report generation.
Sequencing principles, experimental design. Assessing read quality, adapter trimming, quality filtering, and batch QC assessment.
Reference-based alignment · SAM/BAM manipulation · Read counting approaches (TPM, RPKM) · Building count matrices.
Statistical frameworks for differential expression · Normalization · Multiple testing · Gene Ontology · Pathway analysis.
Assembly strategies for plant and non-model organisms · Quality assessment of assemblies · Annotation approaches.
Complete independent RNA-Seq analysis — QC, alignment, quantification, differential expression, pathway interpretation. Submitted as a written report with reproducible code.
Droplet-based sequencing concepts · Count matrices · Cell quality metrics · Filtering low-quality cells, empty droplets, and doublets.
Single cell normalization approaches · Identifying highly variable features · PCA concepts · UMAP and tSNE interpretation.
Graph-based clustering · Evaluating cluster stability · Using known marker genes for manual annotation · Reference-based automated annotation.
Identifying marker genes per cluster · Statistical considerations specific to scRNA-Seq · Visualizing gene expression across cell types.
Complete independent analysis — QC, normalization, dimensionality reduction, clustering, annotation, and marker gene identification. Submitted as a written report with reproducible code.
Quick, practical skills for researchers who already have data
Setting up the environment · Loading and inspecting omics datasets · Basic data cleaning and formatting.
Choosing the right test (t-test, ANOVA, chi-square) · Multiple testing correction · Interpreting p-values correctly.
Heatmaps · Volcano plots · PCA plots · Boxplots and violin plots · Bar charts · All figures styled for publication.
Take a provided omics dataset, apply appropriate statistical tests, generate a set of publication-ready figures, and write a short results section.
Loading count matrix data into an analysis environment · Understanding QC metrics · Filtering decisions · Normalization.
Running and interpreting PCA · Generating UMAP representations · Clustering and understanding resolution.
Identifying cell types using known marker genes · Visualizing gene expression across clusters · Interpreting results.
Take a provided single cell count matrix through QC, normalization, UMAP generation, clustering, and basic annotation to produce a set of publication-ready figures.
Express Track is designed for researchers — no coding background needed for the stats module
Every design decision serves one goal — students who can actually do the work.
Curriculum is built on published research pipelines, not textbook examples. Real data, real problems.
Independent certificate per tier with duration. Join at your level and progress at your own pace.
Directly addresses the practical bioinformatics gap in Indian universities. Built for Indian students and researchers.
Online and in-person (Jaipur). Capstone projects with reproducible code submissions — portfolio-ready outcomes.
You learn concepts and workflows, not just one tool. Skills that transfer as the field evolves.
Start with the foundations week at no cost. Get a real taste before committing to paid tiers.
PhD in Bioinformatics from CSIR-IHBT, Palampur and former Postdoctoral Researcher at the University of Southern California (Mangul Lab, School of Pharmacy), Dr. Sharma brings genuine research experience to every course module.
His published work spans metagenomics benchmarking (MetaWiz), RNA-binding protein prediction, genome assembly of endangered Himalayan plants, wastewater SARS-CoV-2 surveillance, and machine learning in clinical data. Publications in Nature Reviews Methods Primers, iScience, Scientific Reports, PLoS ONE and more.
OmicsWare was born from a simple observation: most Indian biology graduates can describe bioinformatics workflows but cannot actually run them. Every tier is designed to close that gap.
Every topic is grounded in real biological data and real workflows — from day one. Our students don't just learn concepts; they build the computational toolkit that research careers actually demand.
Tier 0 is free — the best way to experience OmicsWare before committing to a paid tier. Reach out with any questions about the program.
Jaipur, Rajasthan, India
Hybrid delivery — online & in-person
Independent certifications · Stackable tiers
Targeted at UG, MSc and PhD students
Send an email to get details about the next cohort, pricing, and how to enroll in Tier 0.
Send Enrollment Email →Tier 0 — Foundations of Bioinformatics — is free to join