Live read stream
Coverage depth
AI pipeline
Aligning reads
EST. 2012 Deep-Tech Genomics Enterprise

Decode everygenomewith precision.

Built in Hyderabad, trusted by 532+ institutions worldwide — AI/ML-ready sequencing and bioinformatics on one integrated, in-house multi-platform stack.

HiFi Long Read→Ultra-Long Nanopore→Short Read
Research partner toSanger InstituteMax Planck InstituteNHGRIRockefeller UniversityVGP
Since 2012
0+
Years of genomics execution
Founded in Hyderabad, India
2012 2019 2025 2026
Worldwide
0+
Institutions & organizations served
Research
0+
Publications with academic rigour
In-house
0
Sequencing platforms
PacBioONTThermo FisherIllumina

Powered by world-class technology partners

PacBioThermo Fisher ScientificQIAGENAgilentRocheDovetailPhase GenomicsZYMO ResearchTakaraDiagenodeIllumina

Six omics platforms,
one seamless workflow

From genomes to proteins, every platform shares the same quality-controlled pipeline — designed for researchers who need depth, speed and reproducibility.

01

Genomics

Pan-genome & de novo assembly, resequencing, optical mapping and single-cell DNA.

De novoPan-genomeGBS
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02

Transcriptomics

mRNA, small RNA, whole-transcriptome, single-cell and circular RNA profiling.

mRNA-SeqscRNAcircRNA
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03

Metagenomics

Shotgun, 16S rRNA, metatranscriptome, microbial and viral genome sequencing.

Shotgun16S rRNAViral
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04

Epigenomics

WGBS, RRBS, ChIP-Seq and targeted methylation panels for regulatory insight.

WGBSRRBSChIP-Seq
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05

Proteomics

Global discovery, quantitative, PTM and protein–protein interaction analysis.

PTMPPIBiomarkers
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06

Metabolomics

Small-molecule profiling that reveals biochemical activity and pathways — services launching soon.

MetabolitesPathwaysComing soon
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Solving complex biological questions through precision genomics

We combine high-throughput sequencing with computational analysis to interpret complex biological data and accelerate discovery across life-science domains.

  • PacBio HiFi, Oxford Nanopore and short-read platforms
  • Rigorous QC at every stage, flagged — never silently carried forward
  • AI-assisted interpretation and multi-omics integration
  • Secure delivery of raw, intermediate and final data
See How We Work →
Figure 1 Sample-to-insight pipeline Infographic
Sample Sequencing $ align --qc ✓ reads trimmed ✓ variants called Bioinformatics Actionable insight Annotated reports · DE · variants · pathways
Figure 1 | From tube to answer. Every project runs through quality-gated sequencing and analysis, ending in reports built for biological interpretation.
1

Consult & design

We shape the study around your objectives, organism and samples.

2

Sample to sequence

Library prep and sequencing on the right platform for the question.

3

Compute & analyse

Alignment, assembly, variant calling and expression analysis.

4

Insight & delivery

AI-driven interpretation and integrated, publication-ready outputs.

From rare disease to oncology —
answers in the genome

Clinically focused panels and whole-genome assays that support diagnosis, prognosis and personalised care.

Rare Disease

Inherited Disorders

Comprehensive screening to uncover the genetic basis of rare and inherited conditions.

Oncology

Cancer Genomics

Tumour profiling and liquid-biopsy assays that guide targeted therapy decisions.

Figure 2 Multi-omics, one sample Schematic
Figure 2 | Integrated view. Genome, transcriptome, epigenome, proteome and microbiome data converge in a single analysis layer.

One integrated, in-house platform stack

HiFi long read, ultra-long nanopore and short read, with automated sample and library prep — all under one roof in Hyderabad, matched to each study design.

Our major focus

AI/ML-ready from the first read. In 2019 we installed the first PacBio Sequel II in South Asia.

Rare DiseaseOncologyMultiomics Studies
PacBio RevioHiFi long read
PacBio Sequel IILong read
ONT PromethION 2iUltra-long read
Ion S5 GeneStudio PlusTargeted NGS
GeneTitan (Thermo Fisher)Microarray
Illumina NovaSeqShort read