DbVar and DGVa: public archives for genomic structural variation (Q28710183)

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scientific article (publication date: 2013)

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English	DbVar and DGVa: public archives for genomic structural variation	scientific article (publication date: 2013)

Statements

instance of

scholarly article

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title

DbVar and DGVa: public archives for genomic structural variation (English)

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author

Ilkka Lappalainen

series ordinal

1

object named as

Ilkka Lappalainen

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John Garner

object named as

John Garner

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6

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Dylan Spalding

object named as

J Dylan Spalding

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5

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Lisa Skipper

object named as

Lisa Skipper

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3

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Paul Flicek

object named as

Paul Flicek

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13

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Deanna M. Church

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14

object named as

Deanna M Church

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author name string

John Lopez

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2

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Timothy Hefferon

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4

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Chao Chen

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7

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Michael Maguire

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8

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Matt Corbett

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9

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George Zhou

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10

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Justin Paschall

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11

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Victor Ananiev

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12

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language of work or name

English

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publication date

January 2013

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published in

Nucleic Acids Research

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volume

41

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issue

Database issue

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page(s)

D936-41

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copyright license

Creative Commons Attribution-NonCommercial 3.0 Unported

start time

4 October 2016

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stated in

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

Database resources of the National Center for Biotechnology Information

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

17 March 2017

Ensembl 2012

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

17 March 2017

The International Nucleotide Sequence Database Collaboration

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

17 March 2017

Mapping copy number variation by population-scale genome sequencing

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

17 March 2017

A map of human genome variation from population-scale sequencing

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

17 March 2017

COSMIC: mining complete cancer genomes in the Catalogue of Somatic Mutations in Cancer

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

17 March 2017

Prepublication data sharing

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

17 March 2017

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

17 March 2017

A standard variation file format for human genome sequences

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

17 March 2017

A copy number variation morbidity map of developmental delay

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

7 April 2017

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

7 April 2017

The fine-scale architecture of structural variants in 17 mouse genomes

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

3 June 2018

Copy number variation of individual cattle genomes using next-generation sequencing

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

3 June 2018

Genome-wide patterns of genetic variation in sweet and grain sorghum (Sorghum bicolor).

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

3 June 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

3 June 2018

Genome structural variation discovery and genotyping

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

3 June 2018

Public data archives for genomic structural variation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

3 June 2018

The human phenotype ontology.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

3 June 2018

Mouse segmental duplication and copy number variation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

3 June 2018

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

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3531204

retrieved

3 June 2018

Identifiers

DOI

10.1093/NAR/GKS1213

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1029999

DBLP publication ID

journals/nar/LappalainenLSHSGCMCZPAFC13

1 reference

stated in

DBLP Dataset 2021-01-02

retrieved

28 January 2021

OpenCitations bibliographic resource ID

1029999

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1029999

PMC publication ID

3531204

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1029999

PubMed publication ID

23193291

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1029999

ResearchGate publication ID

233799072

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