(Q28584449)

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Ensembl 2017

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scholarly article

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28 March 2020

Ensembl 2017 (English)

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28 March 2020

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28 March 2020

Thibaut Hourlier

14

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28 March 2020

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28 March 2020

Premanand Achuthan

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28 March 2020

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28 March 2020

Friederike Bernsdorff

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28 March 2020

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28 March 2020

Konstantinos Billis

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28 March 2020

Denise Carvalho Silva

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28 March 2020

Carla A Cummins

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28 March 2020

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28 March 2020

Carlos García Girón

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28 March 2020

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28 March 2020

Sophie Helen Janacek

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28 March 2020

Thomas Juettemann

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28 March 2020

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28 March 2020

Matthew R Laird

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28 March 2020

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28 March 2020

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28 March 2020

William M McLaren

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28 March 2020

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28 March 2020

Daniel N Murphy

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28 March 2020

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28 March 2020

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28 March 2020

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28 March 2020

Mateus Patricio

30

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28 March 2020

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28 March 2020

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28 March 2020

Alessandro Vullo

36

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28 March 2020

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28 March 2020

Steven P Wilder

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28 March 2020

Amonida Zadissa

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28 March 2020

Myrto Kostadima

40

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28 March 2020

Fergal J Martin

41

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28 March 2020

Matthieu Muffato

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28 March 2020

Emily Pritchard

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28 March 2020

Daniel M Staines

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28 March 2020

Stephen Trevanion

46

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28 March 2020

Fiona Cunningham

47

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28 March 2020

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28 March 2020

Daniel R Zerbino

49

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28 March 2020

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28 March 2020

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M Ridwan Amode

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Harpreet Singh Riat

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Harpreet Singh Riat

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28 March 2020

Daniel J Sheppard

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Daniel Sheppard

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Helen Sparrow

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28 March 2020

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Peter Clapham

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28 March 2020

Leo Gordon

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28 March 2020

Victoria Newman

26

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28 March 2020

Anne Parker

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28 March 2020

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28 November 2016

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28 March 2020

Nucleic Acids Research

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28 March 2020

45

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28 March 2020

D1

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28 March 2020

copyright license

Creative Commons Attribution 4.0 International

2 December 2016

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April 2022 Public Data File from Crossref

copyright status

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Analysis of protein-coding genetic variation in 60,706 humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

17 March 2017

Reference sequence (RefSeq) database at NCBI: current status, taxonomic expansion, and functional annotation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

17 March 2017

A global reference for human genetic variation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

17 March 2017

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

1 reference

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17 March 2017

1 reference

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17 March 2017

The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data

1 reference

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17 March 2017

TreeFam v9: a new website, more species and orthology-on-the-fly

1 reference

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17 March 2017

GENCODE: the reference human genome annotation for The ENCODE Project

1 reference

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17 March 2017

An integrated encyclopedia of DNA elements in the human genome

1 reference

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17 March 2017

The 1000 Genomes Project: data management and community access

1 reference

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17 March 2017

Modernizing reference genome assemblies

1 reference

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17 March 2017

Ensembl variation resources

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

17 March 2017

Modeling sample variables with an Experimental Factor Ontology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

17 March 2017

Genome-wide nucleotide-level mammalian ancestor reconstruction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

17 March 2017

Enredo and Pecan: genome-wide mammalian consistency-based multiple alignment with paralogs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

17 March 2017

Haploview: analysis and visualization of LD and haplotype maps

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

17 March 2017

The Ensembl core software libraries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

17 March 2017

UniProt: a hub for protein information

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

7 April 2017

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

7 April 2017

Mouse genomic variation and its effect on phenotypes and gene regulation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

7 April 2017

The NIH Roadmap Epigenomics Mapping Consortium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

7 April 2017

The Ensembl gene annotation system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

GENOMICS. A federated ecosystem for sharing genomic, clinical data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

The Ensembl Variant Effect Predictor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

Ensembl comparative genomics resources

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

Ensembl regulation resources

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

Wasabi: An Integrated Platform for Evolutionary Sequence Analysis and Data Visualization.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

The UCSC Genome Browser database: 2016 update

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

Improving the Sequence Ontology terminology for genomic variant annotation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

The Mouse Genomes Project: a repository of inbred laboratory mouse strain genomes

1 reference

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29 September 2017

Comparison of GENCODE and RefSeq gene annotation and the impact of reference geneset on variant effect prediction

1 reference

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29 September 2017

WGE: a CRISPR database for genome engineering

1 reference

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29 September 2017

Human genomics. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

The ensembl regulatory build

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

A comprehensive evaluation of ensembl, RefSeq, and UCSC annotations in the context of RNA-seq read mapping and gene quantification

1 reference

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29 September 2017

OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

The Rat Genome Database 2015: genomic, phenotypic and environmental variations and disease

1 reference

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29 September 2017

The Ensembl REST API: Ensembl Data for Any Language

1 reference

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29 September 2017

Choice of transcripts and software has a large effect on variant annotation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

The Vertebrate Genome Annotation browser 10 years on

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

ClinVar: public archive of relationships among sequence variation and human phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

Track data hubs enable visualization of user-defined genome-wide annotations on the UCSC Genome Browser

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

APPRIS: annotation of principal and alternative splice isoforms

1 reference

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29 September 2017

ZFIN, the Zebrafish Model Organism Database: increased support for mutants and transgenics

1 reference

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29 September 2017

Representation of rare diseases in health information systems: the Orphanet approach to serve a wide range of end users

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

Ensembl BioMarts: a hub for data retrieval across taxonomic space

1 reference

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29 September 2017

eHive: an artificial intelligence workflow system for genomic analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

29 September 2017

Using caching and optimization techniques to improve performance of the Ensembl website

1 reference

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29 September 2017

Predicting functional effect of human missense mutations using PolyPhen-2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

3 June 2018

Database resources of the National Center for Biotechnology Information

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

27 November 2018

BLUEPRINT to decode the epigenetic signature written in blood.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

27 November 2018

Aligning multiple whole genomes with Mercator and MAVID.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5210575

27 November 2018

Identifiers

10.1093/NAR/GKW1104

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27899575%20AND%20SRC:MED&resulttype=core&format=json

28 March 2020

DBLP publication ID

journals/nar/AkenAAABBBCCCGG17

1 reference

DBLP Dataset 2021-01-02

28 January 2021

release_hzc4nlutrnfo5obbhqtlljr724

1 reference

https://api.fatcat.wiki/v0/release/hzc4nlutrnfo5obbhqtlljr724

24 November 2022

based on heuristic

mapped directly with Wikidata item

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27899575%20AND%20SRC:MED&resulttype=core&format=json

28 March 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27899575%20AND%20SRC:MED&resulttype=core&format=json

28 March 2020

Sitelinks

Wikipedia(0 entries)

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Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

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