(Q25257137)

6 July 2017

SNP500Cancer: a public resource for sequence validation, assay development, and frequency analysis for genetic variation in candidate genes (English)

1 reference

6 July 2017

1 reference

2

Meredith Yeager

0 references

Stephen Chanock

14

object named as

Stephen J Chanock

1 reference

6 July 2017

1

Bernice R Packer

1 reference

6 July 2017

12

Vinita Puri

1 reference

6 July 2017

3

Laura Burdett

1 reference

6 July 2017

7

Hugues Sicotte

1 reference

6 July 2017

8

Brian Staats

1 reference

6 July 2017

11

Andrew Eckert

1 reference

6 July 2017

Robert Welch

4

1 reference

6 July 2017

Michael Beerman

5

1 reference

6 July 2017

Liqun Qi

6

1 reference

6 July 2017

Mekhala Acharya

9

1 reference

6 July 2017

Andrew Crenshaw

10

1 reference

6 July 2017

Daniela S Gerhard

13

1 reference

6 July 2017

language of work or name

English

0 references

publication date

1 January 2006

1 reference

6 July 2017

Nucleic Acids Research

1 reference

6 July 2017

34

1 reference

6 July 2017

D617-21

1 reference

6 July 2017

Database issue

1 reference

A haplotype map of the human genome

6 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

Entrez Gene: gene-centered information at NCBI

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

Database resources of the National Center for Biotechnology Information

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

dbSNP: the NCBI database of genetic variation

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

Gene ontology: tool for the unification of biology

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

Haploview: analysis and visualization of LD and haplotype maps

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

Primer3 on the WWW for general users and for biologist programmers

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

A human genome diversity cell line panel

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

Genetic variation, nucleotide diversity, and linkage disequilibrium in seven telomere stability genes suggest that these genes may be under constraint

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

Effects of natural selection on interpopulation divergence at polymorphic sites in human protein-coding Loci

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

Cyberinfrastructure: empowering a "third way" in biomedical research

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

SNP500Cancer: a public resource for sequence validation and assay development for genetic variation in candidate genes

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

Widespread purifying selection at polymorphic sites in human protein-coding loci

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

Modeling and E-M estimation of haplotype-specific relative risks from genotype data for a case-control study of unrelated individuals

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

Sequence-based cancer genomics: progress, lessons and opportunities

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

Comparison of yield and genotyping performance of multiple displacement amplification and OmniPlex whole genome amplified DNA generated from multiple DNA sources.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1347513

Genewindow: an interactive tool for visualization of genomic variation

28 November 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16381944

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Sequence analysis of the mannose-binding lectin (MBL2) gene reveals a high degree of heterozygosity with evidence of selection

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16381944

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/NAR/GKJ151

1 reference

journals/nar/PackerYBWBQSSACEPGC06

6 July 2017

1 reference

DBLP Dataset 2021-01-02

release_c5jvmmqe5vdhzmkvaczjjxfkzu

28 January 2021

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/c5jvmmqe5vdhzmkvaczjjxfkzu

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMCID

1347513

1 reference

6 July 2017

1 reference