BioDiscovery

Nexus DB

Searchable reference data that can be integrated with your own Nexus projects.

Nexus DB Benefits

Nexus DB is an invaluable resource and included with all Nexus Copy Number subscriptions.

Store Your Own Data

NexusDB-1

As a Nexus user, you can use NexusDB to store your own data, privately. Data is secured off-site using Amazon’s AWS platform.

Reference Data

NexusDB-3

Query by gene or region of interest to quickly find samples and clinical annotations, with the ability to compare data generated by different aCGH, SNP array, and NGS platforms.

Share and Collaborate

NexusDB-3

Ability to share your own data easily with the people you choose and collaborate across the globe.

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Available Data In Nexus DB

Constitutional Genetics
  • AGRE – Autism Genetic Research Exchange. All data available in both HG18 and HG19 genome builds.
  • ISCA/ICCG (dbVAR) – Structural variation (SV) database of genomic variants with clinical annotations for a broad range of constitutional genetic disorders.
  • Developmental Delay project – a CNV morbidity map of developmental delays.
  • Definitive haplotypes from a collection of complete hydatidiform moles (CHMs)
  • Genotyping data from 54 patients with deficit schizophrenia
Cancer
  • TCGA – Level 3 (segmented) data for select data sets
  • TCGA Premier – reprocessed and manually curated TCGA data, resulting in dramatically increased fidelity and corresponding reduction in false-positive calls.
  • Glioblastoma (GBM)
  • Ovarian Serous Cyst adenocarcinoma
  • Kidney Renal Clear Cell Carcinoma
  • Colon Adenocarcinoma
  • Uterine Corpus Edometrioid carcinoma
  • Head and neck squamous carcinoma
  • Lung squamous carcinoma
  • Thyroid carcinoma

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BioDiscovery Benefits

BioDiscovery provides a full line of modular software packages.

Versatility

Able to handle and process data from all commercial platforms.

Efficiency

Optimum usage of computing.

Acute Sense of Fitness for Purpose

Usefulness to our community of users.

These products empower Biologists and Geneticists with sophisticated, yet highly usable tools to analyze and interpret their data and draw meaningful conclusions.