Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 97

Similar articles for PubMed (Select 21275337)

1.

Microarrays for personalized genomic medicine.

Lam CW, Lau KC, Tong SF.

Adv Clin Chem. 2010;52:1-18. Review.

PMID:
21275337
2.

A fast modified protocol for random-access ultra-high density whole-genome scan: a tool for personalized genomic medicine, positional mapping, and cytogenetic analysis.

Lau KC, Mak CM, Leung KY, Tsoi TH, Tang HY, Lee P, Lam CW.

Clin Chim Acta. 2009 Aug;406(1-2):31-5. doi: 10.1016/j.cca.2009.05.005. Epub 2009 May 13.

PMID:
19445911
3.

Dynamic model based algorithms for screening and genotyping over 100 K SNPs on oligonucleotide microarrays.

Di X, Matsuzaki H, Webster TA, Hubbell E, Liu G, Dong S, Bartell D, Huang J, Chiles R, Yang G, Shen MM, Kulp D, Kennedy GC, Mei R, Jones KW, Cawley S.

Bioinformatics. 2005 May 1;21(9):1958-63. Epub 2005 Jan 18.

4.

A multi-array multi-SNP genotyping algorithm for Affymetrix SNP microarrays.

Xiao Y, Segal MR, Yang YH, Yeh RF.

Bioinformatics. 2007 Jun 15;23(12):1459-67. Epub 2007 Apr 25.

5.

[Genomic medicine. Polymorphisms and microarray applications].

Spalvieri MP, Rotenberg RG.

Medicina (B Aires). 2004;64(6):533-42. Review. Spanish.

PMID:
15637833
6.

SNiPer-HD: improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arrays.

Hua J, Craig DW, Brun M, Webster J, Zismann V, Tembe W, Joshipura K, Huentelman MJ, Dougherty ER, Stephan DA.

Bioinformatics. 2007 Jan 1;23(1):57-63. Epub 2006 Oct 24.

7.

Family-based association tests for genomewide association scans.

Chen WM, Abecasis GR.

Am J Hum Genet. 2007 Nov;81(5):913-26. Epub 2007 Sep 18.

8.

Applications of whole-genome high-density SNP genotyping.

Craig DW, Stephan DA.

Expert Rev Mol Diagn. 2005 Mar;5(2):159-70. Review.

PMID:
15833046
9.
10.

Microarray-based genome-wide association studies using pooled DNA.

Szelinger S, Pearson JV, Craig DW.

Methods Mol Biol. 2011;700:49-60. doi: 10.1007/978-1-61737-954-3_4. Review.

PMID:
21204026
11.

Accuracy of genome-wide imputation of untyped markers and impacts on statistical power for association studies.

Hao K, Chudin E, McElwee J, Schadt EE.

BMC Genet. 2009 Jun 16;10:27. doi: 10.1186/1471-2156-10-27.

12.

[Host genetic epidemiology by single nucleotide polymorphism(SNP) analysis].

Shin HD.

Exp Mol Med. 2001 Apr 21;33(1 Suppl):51-69. Korean.

13.

Theoretical aspects of genomic variation screening using DNA microarrays.

Vainrub A, Pettitt BM.

Biopolymers. 2004 Apr 5;73(5):614-20.

PMID:
15048785
14.

Unlocking the potential of genomic technologies for wildlife forensics.

Ogden R.

Mol Ecol Resour. 2011 Mar;11 Suppl 1:109-16. doi: 10.1111/j.1755-0998.2010.02954.x.

PMID:
21429167
15.

SNP genotyping by multiplex amplification and microarrays assay for forensic application.

Li L, Li CT, Li RY, Liu Y, Lin Y, Que TZ, Sun MQ, Li Y.

Forensic Sci Int. 2006 Oct 16;162(1-3):74-9. Epub 2006 Aug 1.

PMID:
16884875
16.

A semi-automated system for analysis and storage of SNPs.

Lehnert V, Holzwarth J, Ott M, Thompson A, Demmak S, Foernzler D.

Hum Mutat. 2001 Apr;17(4):243-54.

PMID:
11295821
17.

[Single nucleotide polymorphism (SNP) and its application in rice].

Liu CG, Zhang GQ.

Yi Chuan. 2006 Jun;28(6):737-44. Review. Chinese.

PMID:
16818440
18.

A procedure for the detection of linkage with high density SNP arrays in a large pedigree with colorectal cancer.

Middeldorp A, Jagmohan-Changur S, Helmer Q, van der Klift HM, Tops CM, Vasen HF, Devilee P, Morreau H, Houwing-Duistermaat JJ, Wijnen JT, van Wezel T.

BMC Cancer. 2007 Jan 12;7:6.

19.

Genotyping single nucleotide polymorphisms by MALDI mass spectrometry in clinical applications.

Tost J, Gut IG.

Clin Biochem. 2005 Apr;38(4):335-50. Review.

PMID:
15766735
20.

Deletion mapping in Xp21 for patients with complex glycerol kinase deficiency using SNP mapping arrays.

Stanczak CM, Chen Z, Zhang YH, Nelson SF, McCabe ER.

Hum Mutat. 2007 Mar;28(3):235-42.

PMID:
17089405
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk