Search
Product
About us
Contact
Blog

DVD

Names
More detailed information about this field from each metasource.

DVD
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:57.636780

dvd
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:57.636780

Other names: dvd

Names

More detailed information about this field from each metasource.

DVD

metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:57.636780

dvd

metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:57.636780

Diagnostic Variant Database (DVD) is a nation-wide human genomic variant database launched by Dutch University Medical Centers. Its purpose is to share all genetic variants detected in the course of next-generation sequencing (NGS) applications between collaborators. It helps medical researchers to distinguish between functionally relevant and benign genetic variants. DVD also allows users to contact the researcher who originally identified a particular genetic mutation.

Description

More detailed information about this field from each metasource.

Diagnostic Variant Database (DVD) is a nation-wide human genomic variant database launched by Dutch University Medical Centers. Its purpose is to share all genetic variants detected in the course of next-generation sequencing (NGS) applications between collaborators. It helps medical researchers to distinguish between functionally relevant and benign genetic variants. DVD also allows users to contact the researcher who originally identified a particular genetic mutation.

metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:57.636780

Webpage:

https://trac.nbic.nl/dvd/

Webpage

More detailed information about this field from each metasource.

https://trac.nbic.nl/dvd/

metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:57.636780

Licence:

Name: Unlicense

Licence name

More detailed information about this field from each metasource.

Unlicense

metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:57.636780

Tags:

Tags
More detailed information about this field from each metasource.

human genetics
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:57.636780

data integration and warehousing
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:57.636780

genetic variation
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:57.636780

rare diseases
metasource: bio.tools
version: extracted_at: 2022-11-04T11:30:57.636780

human genetics data integration and warehousing genetic variation rare diseases

More to explore:

1/20

Bibliome Variant Database

The Bibliome Variant Database is a collection of variants mined from open-access primary literature. All variants included in the database have been mapped to the human genome and are presented in a m ...

CODEX

ChIP-Seq, RNA-Seq and DNase-Seq data for haematopoietic and embryonic stem cells

dbNSFP

Database developed for functional prediction and annotation of all potential non-synonymous single-nucleotide variants (nsSNVs) and splice-site variants (ssSNVs) in the human genome. It also facilitat ...

Minimum Information for Reporting Next Generation Sequencing Genotyping

MIRING defines the minimum information needed to describe genotyping results for HLA and KIR genes generated using Next Generation Sequencing (NGS) methods, allowing reinterpretation in light of conti ...

CentoMD

Genetic mutation database for rare diseases that enables to search, sort and filter genetic variants from clinically diagnosed individuals worldwide and make symptoms-based queries.

gnomAD

Genome Aggregation Database (gnomAD) - browser that aggregates exome and whole-genome sequencing data from a wide variety of large-scale sequencing projects. It enables search of genetic variation inf ...

The conserved clinical variation visualization tool

The availability of genetic variants, together with phenotypic annotations from model organisms, facilitates comparing these variants with equivalent variants in humans. However, existing databases an ...

Human Genetic Variation Database

The Human Genetic Variation Database (HGVD) aims to provide a central resource to archive and display Japanese genetic variation and association between the variation and transcription level of genes. ...

HGMD

The Human Gene Mutation Database (HGMD) - comprehensive collection of germline mutations in nuclear genes that underlie, or are associated with, human inherited disease. It is a flexible resource that ...

Clinical NGS DB

Tool for the Unified Management of Clinical Information and Genetic Variants to Accelerate Variant Pathogenicity Classification.

PhenoModifier

PhenoModifier is a genetic modifier database for elucidating the genetic basis of human phenotypic variation. PhenoModifier provides a more complete spectrum of genetic factors contributing to human p ...

Database of Genomic Variants

The Database of Genomic Variants (DGV) is a publicly accessible, comprehensive curated catalogue of structural variation (SV) found in the genomes of control individuals from worldwide populations.

Rice Genome Hub

An open source database(s) for genetics, genomics and functional research in rice species

PhenomeCentral

Repository for clinicians and scientists working in the rare disorder community. It enables secure sharing of case records by clinicians and rare disease scientists and helps the user to find addition ...

VarSome

A search engine for human genomic variants.

Diseasecard

Information retrieval tool for accessing and integrating genetic and medical information for health applications. Resorting to this integrated environment, clinicians are able to access and relate dis ...

Alamut

Software that includes powerful bioinformatics applications for genetic analysis and offers a comprehensive solution to the tasks of genomic variants annotation, filtration, interpretation and reporti ...

al MENA

Middle East and North Africa (MENA) encompass very unique populations, with a rich history and encompasses characteristic ethnic, linguistic and genetic diversity. The genetic diversity of MENA region ...

European Variation Archive

The European Variation Archive is an open-access archive that accepts submission of, and provides access to, all types of genetic variation data from all species. All users are able to download any da ...

RNA Binding Protein Variant Database

RBP-Var is a database of functional variants involved in regulation mediated by RNA-binding proteins. Human genome variants can change the RNA structure and affect RNA-protein interactions.

Previous Next

Need help integrating and/or managing biomedical data?