Decoding complex genomic data for
actionable clinical insights
  • Subscribe
    Subscribe

    Select your subscription plan to get started. Contact sales@genome.com

  • Upload Files
    Upload Files

    Multiple upload options for FastQ and VCF file formats

  • Select Objective
    Select Objective

    Choose relevant objective for analysis

  • Define Parameters
    Define Parameters

    Customize analysis parameters

  • Start Analysis
    Start Analysis

    Analysis starts here !

  • View Reports
    View Reports

    View Reports

A cloud-based clinical genomics platform for precision medicine

Meet Genome Explorer®

A comprehensive clinical genomics decision support platform that empowers hospitals and diagnostic labs to decode complex genomic data for actionable clinical insights

PLATFORMS

Supports all major NGS platforms and can easily adopt new sequencing technologies.

FILE FORMATS

Supports FastQ and VCF file formats.

ANALYSIS WORKFLOW

Customized high throughput NGS analysis workflows for individuals, case-control and family samples, and cohort studies.

GENE PANELS

A single comprehensive platform that supports all industry standard oncology and hereditary panels as well as custom panels.

VARIANT PRIORITIZATION

Powerful and flexible Variant Interpretation & Prioritization (ViP) engine provides clinical grade variants.

CLINICAL REPORTING

Decision support with high impact pathogenic variants, pharmacogenomics evidence, and therapeutic information including FDA approved drugs, and associated side effects.

GUIDELINES

Variant prioritization and interpretation based on ACMG, NCCN, ASCO and ESMO clinical guidelines.

PATHOGEN IDENTIFICATION

Support for ampliseq panels, exomes and whole genomes.

  • Hospitals

    Genome Explorer® enables precision medicine through algorithm-guided genomic assessment of inherited diseases and cancer. It provides innovative, cost-effective, and readily accessible clinical decision support.

    Diagnostic Labs
  • Diagnostic Labs

    The comprehensive platform is empowered with a variety of molecular diagnostic and genetic risk-based tests in multiple disease areas including:

    •Molecular oncology
    •Cancer risk assessment
    •Family analysis
    •Pharmacogenomics tests
    •Non-Invasive Prenatal Tests
    •Cystic fibrosis
    •Other inherited disorders

    Researchers
  • Researchers

    Harness the insight of Genome Explorer® to bring the power of big data genomics to your research.

    Hospitals

Transforming genomic intelligence into targeted therapies

Oncology

For various cancers, the platform supports both commercial panels from Illumina, Ion AmpliSeq, and user-specific custom panels. A wide range of comprehensive and tailored Somatic, Germline and Gene Fusion panels consist of highly curated and validated genes associated with targeted treatments, either FDA-approved or active clinical trials.

Inherited Disorders

Identify specific genetic causes of inherited and metabolic disorders. The platform supports leading industry panels, providing a quick, accurate, and cost-effective method to identify genetic mutations associated with inherited disorders.

GEx KnowledgeBase

GEx knowledgebase acts as an intelligent system to decode the complexities of genomic data.

  • Biological Information

    hg19, dbSNP, OMIM

    Biological Information

    hg19, dbSNP, OMIM

  • Cancer Databases

    COSMIC, ClinVar

    Cancer Databases

    COSMIC, ClinVar

  • Population Frequency Databases

    1000 Genomes, Exome Sequencing project (ESP), Exome Aggregation Consortium (ExAC)

    Population Frequency Databases

    1000 Genomes, Exome Sequencing project (ESP), Exome Aggregation Consortium (ExAC)

  • Curated Publications

    Curated and categorized PubMed evidences for 1,256 diseases, 1,181 gene panels, 7,715 clinically relevant genes, 44,558 curated top-tier disease-driving variants, 291 targeted therapies, 109 drug label annotations and 23 actionable pathways.

    Curated Publications

    Curated and categorized PubMed evidences for 1,256 diseases, 1,181 gene panels, 7,715 clinically relevant genes, 44,558 curated top-tier disease-driving variants, 291 targeted therapies, 109 drug label annotations and 23 actionable pathways.

Clinical guidelines
Analyze individual sample,
case-control, family analysis (Trio) & cohort analysis
Request Demo

Security and Compliance

  • Data at Rest and in Transit

  • Data Privacy / Security*

  • Application Security

As a comprehensive solution, Genome Explorer® is offered on Amazon Web Services (AWS) Cloud platform.

Genome Explorer® application development, cloud deployment, app usage, data transition and processing, and user access are compliant with standard data security and privacy measures.

Genome Explorer® adheres to the AWS Compliance Program.

Data at Rest and in Transit

As a comprehensive solution, Genome Explorer® is offered on Amazon Web Services (AWS) Cloud platform.

Data Privacy / Security*

Genome Explorer® application development, cloud deployment, app usage, data transition and processing, and user access are compliant with standard data security and privacy measures.

Application Security

Genome Explorer® adheres to the AWS Compliance Program.