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

author name string

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

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

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

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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

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

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

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

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Haploview: analysis and visualization of LD and haplotype maps

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6 September 2017

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

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The structure of haplotype blocks in the human genome

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

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NMDA receptors mediate calcium accumulation in myelin during chemical ischaemia

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26 June 2018

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

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

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

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

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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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