About ATGCFLOW

Intelligent Infrastructure for Modern Genomic Analysis

ATGCFLOW is a genomics analysis platform built to simplify how genomic data is processed, analyzed, interpreted, and reported. Instead of requiring users to assemble bioinformatics software, computational infrastructure, databases, and analysis workflows themselves, ATGCFLOW brings these capabilities together in a single environment. Research use only.

Our Team

Founder & Scientific Advisor

The people behind ATGC Flow

Robin Tomar

Founder

ATGCFLOW

Dr. Prabudh Goel

Scientific Advisor

Professor of Paediatric Surgery, All India Institute of Medical Sciences (AIIMS), New Delhi

MCh (Paediatric Surgery, AIIMS, New Delhi) · PDCR (Professional Diploma in Clinical Research) · FICS, FISPU, FIAPS, FMAS, FICRS, FSPU, FEpBio(UNSW), FALS, FAIS, FIAGES

Member, National Guideline Development Group, Department of Health Research, Ministry of Health and Family Welfare, Govt. of India

Chairman, Research and Innovation Pediatric Surgical Society, 2024-25

EC Member, Society of Pediatric Urology, Indian Association of Paediatric Surgeons (SPU-IAPS), 2026-28

EC Member, Indian Association of Paediatric Surgeons, 2023-25

EC Member, Association of Paediatric Surgical Oncology, 2023-24

Our Mission

Our focus is simple: make sophisticated genomic analysis easier to access while maintaining reproducibility, transparency, and scientific rigor. ATGCFLOW is designed around a straightforward experience — upload data, run analysis, annotate, interpret, and report — all from the same platform.

Our Vision

We are building toward a future where genomic analysis can move efficiently from raw data to interpretable research results — a platform that combines scalable computation, evolving genomic knowledge, Artificial Intelligence, and human expertise, rather than leaving these as disconnected pieces of infrastructure.

What You Can Do Today

What You Can Do With ATGCFLOW Today

Upload data, run analysis, annotate, interpret, and report — all from one platform

Whole Exome Analysis

ATGCFLOW currently supports paired-end exome FASTQ analysis through an end-to-end workflow covering alignment, variant calling, annotation, and research classification.

Variant Reanalysis

Existing VCF data can be submitted for re-annotation and re-classification using updated genomic knowledge bases, so previously generated variant data can be evaluated again as genomic knowledge evolves.

AI With Experts in the Loop

We are developing AI-assisted capabilities to help organize genomic evidence, prioritize variants, and accelerate report generation — following a human-in-the-loop model where AI assists researchers, not replaces expert judgment.

Research & Innovation

Designed for Reproducible Genomic Research

Genomic analysis involves more than running a sequence of computational steps. It requires appropriate computational resources, genomic reference data, annotation resources, evolving biological knowledge, and reliable handling of analysis results. ATGCFLOW brings these elements into a unified platform.

Reproducibility — analysis workflows are designed to provide consistent, traceable processing across datasets

Scalable computation — the platform is designed to handle computationally demanding genomic workloads through scalable infrastructure

Continuously evolving knowledge — reanalysis capabilities allow existing data to be evaluated against newer genomic databases and evidence

AI-assisted workflows — Artificial Intelligence assists with evidence organization, prioritization, interpretation, and reporting, while keeping human expertise in the loop

99.5%
Variant Calling
Accuracy
8
Pipeline Steps
Automated stages
20+
Annotations
Data sources
50+ GB
Reference Data
Curated databases
About the Project

One Platform for the Analysis Journey

ATGCFLOW is designed to remove unnecessary complexity from the user's side of genomic analysis

Expanding Beyond Exome Analysis

ATGCFLOW is being developed as a broader genomics platform, with additional capabilities planned across multiple sequencing and molecular technologies — including CNV analysis, targeted gene panels, trio exome, whole genome sequencing, somatic cancer, RNA-seq, and more. Roadmap capabilities are not represented as runnable analyses unless explicitly marked available within the platform.

A Unified Workspace

Rather than manually coordinating different analysis tools, computational environments, annotation resources, and reporting processes, users interact with a single workspace: submit data, choose the analysis, follow the computation, explore the results, and generate the report.

Get in Touch

Have questions about the Products, want to report an issue, or interested in collaborating? Reach out - we read every message.

Contact Us

Explore ATGCFLOW

Discover the platform, start an available analysis, or learn more about our technology and upcoming capabilities.

ATGCFLOW is intended for research use only. Results generated by the platform are not intended to independently establish a clinical diagnosis or replace appropriate professional or laboratory review.