ParaHaplo: A program package for haplotype-based whole-genome association study using parallel computing. (Q37414279)

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scientific article published on 21 October 2009

ParaHaplo: A program package for haplotype-based whole-genome association study using parallel computing

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English	ParaHaplo: A program package for haplotype-based whole-genome association study using parallel computing.	scientific article published on 21 October 2009	ParaHaplo: A program package for haplotype-based whole-genome association study using parallel computing

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scholarly article

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19845960%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

1 reference

Europe PubMed Central

ParaHaplo: A program package for haplotype-based whole-genome association study using parallel computing (English)

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Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19845960%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

parallel computing

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inferred from title

whole genome sequencing

1 reference

based on heuristic

inferred from title

Kazuharu Misawa

1

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19845960%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

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Naoyuki Kamatani

2

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Europe PubMed Central

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10 February 2020

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21 October 2009

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10 February 2020

Source Code for Biology and Medicine

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10 February 2020

4

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10 February 2020

1

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7

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19845960%20AND%20SRC:MED&resulttype=core&format=json

10 February 2020

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Creative Commons Attribution 2.0 Generic

21 October 2009

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April 2022 Public Data File from Crossref

copyright status

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April 2022 Public Data File from Crossref

Analysis of East Asia genetic substructure using genome-wide SNP arrays

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

6 September 2017

Accounting for ancestry: population substructure and genome-wide association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

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Japanese population structure, based on SNP genotypes from 7003 individuals compared to other ethnic groups: effects on population-based association studies

1 reference

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ITPKC functional polymorphism associated with Kawasaki disease susceptibility and formation of coronary artery aneurysms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

6 September 2017

The BioBank Japan Project.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

6 September 2017

D-HaploDB: a database of definitive haplotypes determined by genotyping complete hydatidiform mole samples

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

6 September 2017

The CENP-H-I complex is required for the efficient incorporation of newly synthesized CENP-A into centromeres

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

6 September 2017

Two forms of human Inscuteable-related protein that links Par3 to the Pins homologues LGN and AGS3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

6 September 2017

Genome-wide association studies for common diseases and complex traits

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

6 September 2017

Online Mendelian Inheritance in Man (OMIM), a knowledgebase 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=2774321

6 September 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=2774321

6 September 2017

Assessing the impact of population stratification on genetic association studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

6 September 2017

The International HapMap Project

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

6 September 2017

An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

6 September 2017

The structure of haplotype blocks in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

6 September 2017

Ca(2+)-dependent and -independent activities of neural and non-neural synaptotagmins

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

6 September 2017

Evolutionary Rate at the Molecular Level

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

6 September 2017

Cloning of cDNAs encoding human caldesmons

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

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NMDA receptors mediate calcium accumulation in myelin during chemical ischaemia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

26 June 2018

New correction algorithms for multiple comparisons in case-control multilocus association studies based on haplotypes and diplotype configurations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

2 September 2018

A fast method for computing high-significance disease association in large population-based studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

2 September 2018

Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2774321

2 September 2018

The power of genome-wide association studies of complex disease genes: statistical limitations of indirect approaches using SNP markers

1 reference

https://pubmed.ncbi.nlm.nih.gov/19845960

12 December 2020

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10.1186/1751-0473-4-7

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10 February 2020

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journals/scfbm/MisawaK09

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DBLP Dataset 2021-01-02

28 January 2021

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