Database Commons
Database Commons

a catalog of worldwide biological databases

Database Profile

vizER

General information

URL: http://rytenlab.com/browser/app/vizER
Full name: Visualisation of Expressed Regions
Description: A novel annotation incorporating constrained, non-conserved metrics to highlight human-lineage-specific genomic regions is generated, which prioritises genes and transcripts of relevance to disease, specifically in the identification of functionally important non-coding genomic regions. Thus this online web resource, vizER, is developed with the primary goal of aiding clinical scientists and clinicians to visualise misannotations of any gene of interest, enabling better variant prioritisation and as a result, diagnosis of both Mendelian disorders and complex genetics diseases.
Year founded: 2020
Last update:
Version:
Accessibility:
Accessible
Country/Region: United Kingdom

Classification & Tag

Data type:
DNA
Data object:
Database category:
Major species:
Keywords:

Contact information

University/Institution: University College London
Address: 30 Guilford Street, London WC1N 1EH
City: London
Province/State:
Country/Region: United Kingdom
Contact name (PI/Team): Mina Ryten
Contact email (PI/Helpdesk): mina.ryten@ucl.ac.uk

Publications

Ranking

All databases:
1743/6278 (72.252%)
Gene genome and annotation:
543/1785 (69.636%)
Genotype phenotype and variation:
251/898 (72.16%)
Health and medicine:
405/1501 (73.085%)
1743
Total Rank
22
Citations
5.5
z-index

Community reviews

Not Rated
Data quality & quantity:
Content organization & presentation
System accessibility & reliability:

Word cloud

Created with Highcharts 10.0.0vizERgeneshumanannotationunannotatedtranscriptionunderstandingMendeliandifferentdisorderstissuesgeneremainsbrainreannotatedpreviouslygreatestimpactcomplexneurogeneticIncompletedisproportionateGrowingevidencesuggestsincomplete;howeverunclearaffectsdetectGenotype-TissueExpressionRNAsequencingdataacross41connectknownconfirmingincompleteevenamongwell-studiedincluding63%OnlineInheritanceMan-morbidcatalog317neurodegeneration-associatedfindabundancehighlyexpressedlikelyexploreexamplesdiseaseexperimentallyvalidateunidentifiedbrain-specificpotentiallyprotein-codingexonreleasetissue-specifictranscriptomesvizER:http://rytenlab.com/browser/app/vizERanticipateresourcewillfacilitateaccurategeneticanalysisdisorders.

Related Databases

Citing
Cited by

Record metadata

Created on: 2020-11-07
Curated by:
Lin Liu [2021-03-24]
Ming Chen [2020-11-26]
Ming Chen [2020-11-07]