(Q30490259)

17 October 2017

The cancer precision medicine knowledge base for structured clinical-grade mutations and interpretations (English)

1 reference

17 October 2017

1 reference

7

0 references

Olivier Elemento

11

object named as

Olivier Elemento

0 references

author name string

Linda Huang

1

1 reference

17 October 2017

Helen Fernandes

2

1 reference

17 October 2017

Hamid Zia

3

1 reference

17 October 2017

Peyman Tavassoli

4

1 reference

17 October 2017

Hanna Rennert

5

1 reference

17 October 2017

David Pisapia

6

1 reference

17 October 2017

Andrea Sboner

8

1 reference

17 October 2017

Mark A Rubin

9

1 reference

17 October 2017

Michael Kluk

10

1 reference

17 October 2017

27 October 2016

1 reference

Journal of the American Medical Informatics Association

17 October 2017

1 reference

17 October 2017

24

1 reference

17 October 2017

3

1 reference

17 October 2017

513-519

1 reference

Creative Commons Attribution-NonCommercial 4.0 International

17 October 2017

start time

16 January 2017

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

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=5391733

HGVS Recommendations for the Description of Sequence Variants: 2016 Update

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5391733

Whole-Exome Sequencing of Metastatic Cancer and Biomarkers of Treatment Response.

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5391733

Genenames.org: the HGNC resources in 2015

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5391733

COSMIC: exploring the world's knowledge of somatic mutations in human cancer

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5391733

The Ensembl REST API: Ensembl Data for Any Language

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5391733

Whole-exome sequencing and clinical interpretation of formalin-fixed, paraffin-embedded tumor samples to guide precision cancer medicine

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5391733

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5391733

A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5391733

Personalized oncology through integrative high-throughput sequencing: a pilot study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5391733

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5391733

20 June 2018

Identifiers

DOI

10.1093/JAMIA/OCW148

1 reference

journals/jamia/HuangFZTRPISRKE17

17 October 2017

1 reference

DBLP Dataset 2021-01-02

28 January 2021

1 reference

17 October 2017

PubMed publication ID

27789569

1 reference