(Q37661947)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24174537%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

title

The Database of Genomic Variants: a curated collection of structural variation in the human genome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24174537%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

0 references

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24174537%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

Ryan Yuen

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24174537%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

Stephen W. Scherer

series ordinal

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24174537%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

4

Lars Feuk

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24174537%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

author name string

Robert Ziman

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24174537%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

language of work or name

English

0 references

publication date

29 October 2013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24174537%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

published in

Nucleic Acids Research

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24174537%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

volume

42

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24174537%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

issue

Database issue

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24174537%20AND%20SRC:MED&resulttype=core&format=json

28 February 2020

page(s)

D986-92

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24174537%20AND%20SRC:MED&resulttype=core&format=json

Creative Commons Attribution 3.0 Unported

28 February 2020

copyright license

start time

4 October 2016

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

Diagnostic interpretation of array data using public databases and internet sources

1 reference

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Deep whole-genome sequencing of 100 southeast Asian Malays

23 August 2017

1 reference

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23 August 2017

1 reference

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DbVar and DGVa: public archives for genomic structural variation

23 August 2017

1 reference

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ArrayExpress update--trends in database growth and links to data analysis tools

23 August 2017

1 reference

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NCBI GEO: archive for functional genomics data sets--update

23 August 2017

1 reference

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The UCSC Genome Browser database: extensions and updates 2013.

23 August 2017

1 reference

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An integrated map of genetic variation from 1,092 human genomes

23 August 2017

1 reference

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An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.

23 August 2017

1 reference

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Public data archives for genomic structural variation

23 August 2017

1 reference

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Towards a comprehensive structural variation map of an individual human genome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3965079

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

23 August 2017

1 reference

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Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3965079

The clinical context of copy number variation in the human genome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3965079

Origins and functional impact of copy number variation in the human genome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3965079

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

23 August 2017

1 reference

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Challenges and standards in integrating surveys of structural variation

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3965079

Development of bioinformatics resources for display and analysis of copy number and other structural variants in the human genome.

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3965079

Structural variation in the human genome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3965079

The Sequence Ontology: a tool for the unification of genome annotations

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3965079

Detection of large-scale variation in the human genome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3965079

Large-scale copy number polymorphism in the human genome

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3965079

The generic genome browser: a building block for a model organism system database

23 August 2017

1 reference

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Recent segmental duplications in the human genome

23 August 2017

1 reference

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Database resources of the National Center for Biotechnology Information

23 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3965079

https://api.fatcat.wiki/v0/release/lsdvualfa5bzlptai7uq3oxxdi

1 September 2018

Identifiers

1 reference

30 July 2022

journals/nar/MacDonaldZYFS14

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

release_lsdvualfa5bzlptai7uq3oxxdi

28 January 2021

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/lsdvualfa5bzlptai7uq3oxxdi

30 July 2022

https://api.fatcat.wiki/v0/release/lsdvualfa5bzlptai7uq3oxxdi

1 reference

30 July 2022

https://api.fatcat.wiki/v0/release/lsdvualfa5bzlptai7uq3oxxdi

PubMed publication ID

1 reference

30 July 2022