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Program report: GENECOUNTING support programs

Research output: Contribution to Journal/Magazine › Journal article › peer-review

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Program report: GENECOUNTING support programs. / Curtis, David; Knight, Jo; Sham, Pak C.
In: Annals of Human Genetics, Vol. 70, No. Pt 2, 03.2006, p. 277-279.

Research output: Contribution to Journal/Magazine › Journal article › peer-review

Harvard

Curtis, D, Knight, J & Sham, PC 2006, 'Program report: GENECOUNTING support programs', Annals of Human Genetics, vol. 70, no. Pt 2, pp. 277-279. https://doi.org/10.1111/j.1529-8817.2005.00225.x

APA

Curtis, D., Knight, J., & Sham, P. C. (2006). Program report: GENECOUNTING support programs. Annals of Human Genetics, 70(Pt 2), 277-279. https://doi.org/10.1111/j.1529-8817.2005.00225.x

Vancouver

Curtis D, Knight J, Sham PC. Program report: GENECOUNTING support programs. Annals of Human Genetics. 2006 Mar;70(Pt 2):277-279. Epub 2005 Sept 2. doi: 10.1111/j.1529-8817.2005.00225.x

Author

Curtis, David ; Knight, Jo ; Sham, Pak C. / Program report : GENECOUNTING support programs. In: Annals of Human Genetics. 2006 ; Vol. 70, No. Pt 2. pp. 277-279.

Bibtex

@article{eaa240075857428793f3c4290fcc33ae,
title = "Program report: GENECOUNTING support programs",
abstract = "We describe a suite of programs which enhance the usability of GENECOUNTING, a program for estimating haplotype frequencies in unrelated subjects. The programs, called RUNGC, SCANASSOC, COMPGR, SCANGROUP and LDPAIRS, carry out likelihood ratio tests and permutation tests to detect differences in haplotype frequencies between cases and controls,or between predefined groups, and output likely haplotype assignments and tables of linkage disequilibrium statistics between all pairs of markers in a dataset.",
keywords = "Databases, Genetic, Haplotypes, Humans",
author = "David Curtis and Jo Knight and Sham, {Pak C.}",
year = "2006",
month = mar,
doi = "10.1111/j.1529-8817.2005.00225.x",
language = "English",
volume = "70",
pages = "277--279",
journal = "Annals of Human Genetics",
issn = "0003-4800",
publisher = "Wiley-Blackwell",
number = "Pt 2",

}

RIS

TY - JOUR

T1 - Program report

T2 - GENECOUNTING support programs

AU - Curtis, David

AU - Knight, Jo

AU - Sham, Pak C.

PY - 2006/3

Y1 - 2006/3

N2 - We describe a suite of programs which enhance the usability of GENECOUNTING, a program for estimating haplotype frequencies in unrelated subjects. The programs, called RUNGC, SCANASSOC, COMPGR, SCANGROUP and LDPAIRS, carry out likelihood ratio tests and permutation tests to detect differences in haplotype frequencies between cases and controls,or between predefined groups, and output likely haplotype assignments and tables of linkage disequilibrium statistics between all pairs of markers in a dataset.

AB - We describe a suite of programs which enhance the usability of GENECOUNTING, a program for estimating haplotype frequencies in unrelated subjects. The programs, called RUNGC, SCANASSOC, COMPGR, SCANGROUP and LDPAIRS, carry out likelihood ratio tests and permutation tests to detect differences in haplotype frequencies between cases and controls,or between predefined groups, and output likely haplotype assignments and tables of linkage disequilibrium statistics between all pairs of markers in a dataset.

KW - Databases, Genetic

KW - Haplotypes

KW - Humans

U2 - 10.1111/j.1529-8817.2005.00225.x

DO - 10.1111/j.1529-8817.2005.00225.x

M3 - Journal article

C2 - 16626337

VL - 70

SP - 277

EP - 279

JO - Annals of Human Genetics

JF - Annals of Human Genetics

SN - 0003-4800

IS - Pt 2

ER -