(Q33291242)

25 July 2017

title

Comparison of artificial neural network analysis with other multimarker methods for detecting genetic association (English)

1 reference

artificial neural network

25 July 2017

main subject

1 reference

David Curtis

1

0 references

publication date

18 July 2007

1 reference

25 July 2017

1 reference

25 July 2017

volume

8

1 reference

25 July 2017

page(s)

49

1 reference

Creative Commons Attribution 2.0 Generic

25 July 2017

copyright license

start time

18 July 2007

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

exact match

https://scigraph.springernature.com/pub.10.1186/1471-2156-8-49

0 references

cites work

The ENCODE (ENCyclopedia Of DNA Elements) Project

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1940019

The International HapMap Project

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1940019

Genetic analysis of case/control data using estimated haplotype frequencies: application to APOE locus variation and Alzheimer's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1940019

Detecting disease associations due to linkage disequilibrium using haplotype tags: a class of tests and the determinants of statistical power

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1940019

Pedigree disequilibrium tests for multilocus haplotypes.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1940019

Assessing optimal neural network architecture for identifying disease-associated multi-marker genotypes using a permutation test, and application to calpain 10 polymorphisms associated with diabetes.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1940019

A note on calculation of empirical P values from Monte Carlo procedure

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1940019

GENECOUNTING: haplotype analysis with missing genotypes.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1940019

A note on the calculation of empirical P values from Monte Carlo procedures.

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1940019

Use of an artificial neural network to detect association between a disease and multiple marker genotypes

31 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1940019

Investigation of the Ability of Haplotype Association and Logistic Regression to Identify Associated Susceptibility Loci

31 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17640352

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Program Report: GENECOUNTING Support Programs

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17640352

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2156-8-49

1 reference

Dimensions Publication ID

25 July 2017

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2156-8-49

9 September 2019

1 reference

25 July 2017

1 reference