Note: We provide research & analytics services. Clinical testing and medical decisions are performed by licensed clinicians and accredited laboratories. This page is not medical advice.
Core Capabilities
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NGS Strategy
WES/WGS • RNA-Seq • 16S/shotgun
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Wet-lab Coordination
Partner labs • Sample logistics
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Bioinformatics
GATK • STAR • Salmon • Nextflow
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Variant Interpretation
ACMG/AMP guidelines
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AI Models
Polygenic risk • Predictive scores
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Multi-omics
Genomics • Transcriptomics • Metagenomics
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Privacy & Security
Consent • PHI controls • Audit
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Clinical Partners
Accredited reporting
Validated Pipelines
DNA: WES / WGS Variant Calling
- QC (FastQC/MultiQC), trimming, alignment (BWA-MEM)
- GATK: BQSR, HaplotypeCaller, VQSR
- Annotation (VEP/ANNOVAR), freq DBs, panels
RNA-Seq Differential Expression
- STAR/Salmon quant, normalization
- DESeq2/edgeR, enrichment (GO/KEGG)
- Publication-ready figures & report
Microbiome 16S / Shotgun
- DADA2/QIIME2 workflows, taxonomy
- Alpha/beta diversity, differential abundance
- Diet/lifestyle correlations (research)
Pharmacogenomics (PGx)
- Panel selection & calling (CYP2D6 etc.)
- Phenotype inference, drug-gene mapping
- Clinician summary via partner lab
Start a Project
Contact
FASTQ/VCF upload link is shared after scoping.
Packages
Research
Discovery Consult
₹ 25k — 60k
- Study design, panel selection
- Data QC & feasibility
- 1 research brief + roadmap
Analytics
Bioinformatics Core
₹ 95k — 1.6L
- NGS pipeline + report
- Figures & notebook
- 1 iteration of revisions
Clinical collab
Translational Suite
₹ 1.8L+ / project
- Partner lab workflow
- Clinician-ready summary
- Consent & compliance kit
*Lab & sequencing costs are separate. Final quote post-discovery.
GATK
Nextflow
QIIME2
DESeq2
VEP
ANNOVAR
OpenTelemetry
S3/GCS/Azure