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Results: 1 to 20 of 88

Similar articles for PubMed (Select 19622421)

1.

Variable-length haplotype construction for gene-gene interaction studies: a nonparametric classification approach.

Assawamakin A, Chaiyaratana N, Limwongse C, Sinsomros S, Yenchitsomanus PT, Youngkong P.

IEEE Eng Med Biol Mag. 2009 Jul-Aug;28(4):25-31. doi: 10.1109/MEMB.2009.932902. No abstract available.

PMID:
19622421
2.

Is haplotype block identification useful for association mapping studies?

Zhai W, Todd MJ, Nielsen R.

Genet Epidemiol. 2004 Jul;27(1):80-3. No abstract available.

PMID:
15185406
3.

Pattern-recognition techniques with haplotype analysis in pharmacogenomics.

Lin E, Hwang Y, Liang KH, Chen EY.

Pharmacogenomics. 2007 Jan;8(1):75-83. Review.

PMID:
17187511
4.

A partition-ligation-combination-subdivision EM algorithm for haplotype inference with multiallelic markers: update of the SHEsis (http://analysis.bio-x.cn).

Li Z, Zhang Z, He Z, Tang W, Li T, Zeng Z, He L, Shi Y.

Cell Res. 2009 Apr;19(4):519-23. doi: 10.1038/cr.2009.33. No abstract available.

PMID:
19290020
5.

Possible epistatic role of ADH7 in the protection against alcoholism.

Osier MV, Lu RB, Pakstis AJ, Kidd JR, Huang SY, Kidd KK.

Am J Med Genet B Neuropsychiatr Genet. 2004 Apr 1;126B(1):19-22. Review.

PMID:
15048643
6.

Reconstructing ancestral haplotypes with a dictionary model.

Ayers KL, Sabatti C, Lange K.

J Comput Biol. 2006 Apr;13(3):767-85.

PMID:
16706724
7.

Haplotype association of the adrenergic beta2 receptor gene with essential hypertension.

Saleheen D, Merwat S, Frossard P.

J Hum Hypertens. 2006 Feb;20(2):167-8. No abstract available.

PMID:
16252000
8.

Haplotype analysis of beta thalassemia patients in Western Iran.

Rahimi Z, Muniz A, Akramipour R, Tofieghzadeh F, Mozafari H, Vaisi-Raygani A, Parsian A.

Blood Cells Mol Dis. 2009 Mar-Apr;42(2):140-3. doi: 10.1016/j.bcmd.2008.12.001. Epub 2009 Jan 13.

PMID:
19141369
9.

[The questions on the genetic analysis in the study of gene polymorphism related to disease].

Fang FD.

Zhonghua Yi Xue Za Zhi. 2004 May 17;84(10):796-8. Chinese. No abstract available.

PMID:
15200878
10.

Grouping preprocess to accurately extend application of EM algorithm to haplotype inference.

Shindo H, Chigira H, Tanaka J, Kamatani N, Inoue M.

J Hum Genet. 2008;53(8):747-56. doi: 10.1007/s10038-008-0308-9. Epub 2008 Jun 25.

PMID:
18575803
11.

Estimation of recombination rate and detection of recombination hotspots from dense single-nucleotide polymorphism trio data.

Visscher PM, Hill WG.

Genetics. 2006 Aug;173(4):2415-7. Epub 2006 Jun 18. No abstract available.

12.

Computational intelligence in bioinformatics: SNP/haplotype data in genetic association study for common diseases.

Kelemen A, Vasilakos AV, Liang Y.

IEEE Trans Inf Technol Biomed. 2009 Sep;13(5):841-7. doi: 10.1109/TITB.2009.2024144. Epub 2009 Jun 23. Review.

PMID:
19556205
13.

Linear time probabilistic algorithms for the singular haplotype reconstruction problem from SNP fragments.

Chen Z, Fu B, Schweller R, Yang B, Zhao Z, Zhu B.

J Comput Biol. 2008 Jun;15(5):535-46. doi: 10.1089/cmb.2008.0003.

PMID:
18549306
14.

Haplotyping of the deoxycytidine kinase gene by multicapillary electrophoresis.

Szantai E, Ronai Z, Sasvari-Szekely M, Guttman A.

Anal Biochem. 2006 May 1;352(1):148-50. Epub 2006 Feb 8. No abstract available.

PMID:
16527236
15.

Haplotype inference for population data with genotyping errors.

Zhu W, Kuk AY, Guo J.

Biom J. 2009 Aug;51(4):644-58. doi: 10.1002/bimj.200800215.

PMID:
19688759
16.

Detecting interactions in association studies by using simple allele recoding.

Sillanpää MJ.

Hum Hered. 2009;67(1):69-75. doi: 10.1159/000164401. Epub 2008 Oct 17.

PMID:
18931512
17.

The use of inferred haplotypes in downstream analyses.

Lin DY, Huang BE.

Am J Hum Genet. 2007 Mar;80(3):577-9. No abstract available.

18.

A better block partition and ligation strategy for individual haplotyping.

Zhao Y, Xu Y, Wang Z, Zhang H, Chen G.

Bioinformatics. 2008 Dec 1;24(23):2720-5. doi: 10.1093/bioinformatics/btn519. Epub 2008 Oct 9.

19.

PMCHAP: a new approach for haplotype inference using nuclear families with only one parent and multiple offspring.

Ding XD, Zhang Q, Simianer H.

J Anim Breed Genet. 2008 Oct;125(5):339-41. doi: 10.1111/j.1439-0388.2008.00746.x.

PMID:
18803789
20.

Evaluation of Nyholt's procedure for multiple testing correction - author's reply.

Nyholt DR.

Hum Hered. 2005;60(1):61-2. Epub 2005 Aug 5. No abstract available.

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