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

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

10 February 2020

review article

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title

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

1 reference

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

1

1 reference

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

series ordinal

2

1 reference

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

10 February 2020

language of work or name

English

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publication date

21 October 2009

1 reference

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Source Code for Biology and Medicine

10 February 2020

published in

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10 February 2020

volume

4

1 reference

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10 February 2020

page(s)

7

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https://scigraph.springernature.com/pub.10.1186/1751-0473-4-7

10 February 2020

exact match

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cites work

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

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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

6 September 2017

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Evolutionary Rate at the Molecular Level

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Cloning of cDNAs encoding human caldesmons

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NMDA receptors mediate calcium accumulation in myelin during chemical ischaemia

6 September 2017

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

26 June 2018

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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

2 September 2018

1 reference

PubMed

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

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1751-0473-4-7

1 reference

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

10 February 2020

DBLP publication ID

journals/scfbm/MisawaK09

1 reference

DBLP Dataset 2021-01-02

Dimensions Publication ID

28 January 2021

0 references

1 reference

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

10 February 2020

PubMed publication ID

19845960

1 reference