Gene Panels

WES Data

Biospecimens

Patient-Consented Biobank from nference

A rapidly expanding dataset of over 100K individuals, offering deeply integrated genomic and phenotypic insights. Explore high-quality Whole Exome Sequencing (WES) and Gene Panel data to uncover genetic patterns, understand disease mechanisms, and advance precision medicine.

Patient Cohorts with Whole Exome Sequencing Data

By integrating Whole Exome Sequencing data with clinical context, researchers can identify biomarkers, assess disease risk, and develop targeted therapies—driving advancements in precision medicine. At nSights patients with Whole Exome Sequencing data are available across various disease areas, therapies, and drug classes.

15,000+

Obesity Patients

9,000+

Patients with Major Depressive Disorder

13,000+

Patients with Arrhythmia

47,000+

Patients on NSAIDs

3,000+

Patients with Fatty Liver Disease.

300+

Parkinson's Patients

8,000+

Osteoarthritis Patients

4,000+

Patients on GLP-1 Receptor Agonists

6,000+

Type 2 Diabetic Patients

9,000+

Patients with Hypothyroidism

8,000+

Patients with Skin Neoplasms

10,000+

Patients on ACE Inhibitors

And Many More...

Comprehensive & Connected Data

A rapidly expanding dataset of over 100K individuals, offering deeply integrated genomic and phenotypic insights. Explore high-quality Whole Exome Sequencing (WES) and Gene Panel data to uncover genetic patterns, understand disease mechanisms, and advance precision medicine.

Bridging the gap between genomics and clinical insights to accelerate discoveries in precision medicine.

Integrated Genomics at nSights

nSights Federated Clinical Analytics Platform (FCAP) processes genomics data at scale, linking it with patient EMR data for seamless analysis. With integrated genomics, nSights provides access to deep, Multimodal Clinico-Genomic Real-World Data across various therapeutic areas.

~ A growing genomics dataset with 
75K+ Gene Panels, 65K+ Whole Exome Sequences, and 30K+ Biosamples

nference Genomics Data

Complex cohort building and detailed characterization based on comprehensive genomic data.

Review genomic results for individual patients in the context of other clinical events using

AI-driven conversational analysis.

Integrate discovery and analysis with deep clinical phenotypes from EMR data using a self-service analytics workbench

Genomics RWE with nSights

Linked Real World Data in Genomics

Access to millions of EMR- tied patient samples for prospective molecular data generation and analysis.

Multimodal Data powered by Agentic AI

De- identified, longitudinal EMR data (Phenotypic, imaging and genomics) powered with secured Agentic AI tools for rapid insighting

nSights Genomics Data Processing Pipeline

Comprehensive, validated pipeline for genomics data with Variant Calling, Variant Annotation and Integrated Public tools & libraries.

Connect with Us to explore the Nference Patient-consented Biobank