VarCards: an integrated genetic and clinical database for coding variants in the human genome. (Q47097898)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29112736%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

title

VarCards: an integrated genetic and clinical database for coding variants in the human genome (English)

1 reference

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9 April 2020

2

1 reference

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9 April 2020

Huajing Teng

7

1 reference

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9 April 2020

Zhongsheng Sun

11

1 reference

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9 April 2020

Zhongsheng Sun

12

1 reference

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9 April 2020

author name string

Jinchen Li

1

1 reference

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9 April 2020

Kun Zhang

3

1 reference

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9 April 2020

Yi Zhang

4

1 reference

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9 April 2020

Shanshan Hu

5

1 reference

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9 April 2020

Tingting Zhao

6

1 reference

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9 April 2020

Xianfeng Li

8

1 reference

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9 April 2020

Yi Jiang

9

1 reference

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9 April 2020

Liying Ji

10

1 reference

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9 April 2020

language of work or name

English

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publication date

1 January 2018

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9 April 2020

published in

Nucleic Acids Research

1 reference

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9 April 2020

volume

46

1 reference

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9 April 2020

issue

D1

1 reference

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9 April 2020

page(s)

D1039-D1048

1 reference

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Creative Commons Attribution-NonCommercial 4.0 International

9 April 2020

copyright license

start time

3 November 2017

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

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23 May 2018

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23 May 2018

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23 May 2018

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23 May 2018

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A method and server for predicting damaging missense mutations

23 May 2018

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Identification of deleterious mutations within three human genomes

23 May 2018

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

23 May 2018

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Identifying novel constrained elements by exploiting biased substitution patterns

23 May 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5753295

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5753295

Evolutionarily conserved elements in vertebrate, insect, worm, and yeast genomes

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5753295

SIFT: Predicting amino acid changes that affect protein function

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5753295

dbSNP: the NCBI database of genetic variation

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5753295

23 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5753295

M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5753295

SIFT missense predictions for genomes

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5753295

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5753295

Computational techniques for human genome resequencing using mated gapped reads

15 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5753295

New Methods for Detecting Lineage-Specific Selection

15 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FNAR%2FGKX1039

The Genotype-Tissue Expression (GTEx) project

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1093%2FNAR%2FGKX1039

Shotgun sequence assembly and recent segmental duplications within the human genome

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/29112736

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/NAR/GKX1039

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29112736%20AND%20SRC:MED&resulttype=core&format=json

journals/nar/LiSZZHZTLJJS18

9 April 2020

DBLP publication ID

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:29112736%20AND%20SRC:MED&resulttype=core&format=json

9 April 2020

PubMed publication ID

29112736

1 reference