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Results: 1 to 20 of 759

1.

A low-cost, high-throughput, automated single nucleotide polymorphism assay for forensic human DNA applications.

Pomeroy R, Duncan G, Sunar-Reeder B, Ortenberg E, Ketchum M, Wasiluk H, Reeder D.

Anal Biochem. 2009 Dec 1;395(1):61-7. doi: 10.1016/j.ab.2009.07.041. Epub 2009 Jul 30.

PMID:
19646946
[PubMed - indexed for MEDLINE]
2.

Illumina DNA test panel-based genotyping of whole genome amplified-DNA extracted from hair samples: performance and agreement with genotyping results from genomic DNA from buccal cells.

Agalliu I, Schweitzer PA, Leanza SM, Burk RD, Rohan TE.

Clin Chem Lab Med. 2009;47(5):516-22. doi: 10.1515/CCLM.2009.106.

PMID:
19397482
[PubMed - indexed for MEDLINE]
3.

A SNaPshot assay for genotyping 44 individual identification single nucleotide polymorphisms.

Lou C, Cong B, Li S, Fu L, Zhang X, Feng T, Su S, Ma C, Yu F, Ye J, Pei L.

Electrophoresis. 2011 Feb;32(3-4):368-78. doi: 10.1002/elps.201000426. Epub 2010 Dec 30.

PMID:
21298663
[PubMed - indexed for MEDLINE]
4.

[The usefulness of SNP markers for analyses of highly degraded biological materials].

Babol-Pokora K, Prośniak A, Jacewicz R, Berent J.

Arch Med Sadowej Kryminol. 2009 Apr-Jun;59(2):118-23. Polish.

PMID:
20073261
[PubMed - indexed for MEDLINE]
5.

[SNP genotyping by multiplex amplification and microarrays assay and forensic application].

Li L, Li RY, Li CT.

Fa Yi Xue Za Zhi. 2005 May;21(2):90-5. Chinese.

PMID:
15931745
[PubMed - indexed for MEDLINE]
6.

Evaluation of the Genplex SNP typing system and a 49plex forensic marker panel.

Phillips C, Fang R, Ballard D, Fondevila M, Harrison C, Hyland F, Musgrave-Brown E, Proff C, Ramos-Luis E, Sobrino B, Carracedo A, Furtado MR, Syndercombe Court D, Schneider PM; SNPforID Consortium.

Forensic Sci Int Genet. 2007 Jun;1(2):180-5. doi: 10.1016/j.fsigen.2007.02.007. Epub 2007 Mar 23.

PMID:
19083752
[PubMed - indexed for MEDLINE]
7.

Dynamic variable selection in SNP genotype autocalling from APEX microarray data.

Podder M, Welch WJ, Zamar RH, Tebbutt SJ.

BMC Bioinformatics. 2006 Nov 30;7:521.

PMID:
17137502
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

New generation pharmacogenomic tools: a SNP linkage disequilibrium Map, validated SNP assay resource, and high-throughput instrumentation system for large-scale genetic studies.

De La Vega FM, Dailey D, Ziegle J, Williams J, Madden D, Gilbert DA.

Biotechniques. 2002 Jun;Suppl:48-50, 52, 54.

PMID:
12083398
[PubMed - indexed for MEDLINE]
9.

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
[PubMed - indexed for MEDLINE]
10.

Genome-wide single-nucleotide polymorphism arrays demonstrate high fidelity of multiple displacement-based whole-genome amplification.

Tzvetkov MV, Becker C, Kulle B, Nürnberg P, Brockmöller J, Wojnowski L.

Electrophoresis. 2005 Feb;26(3):710-5.

PMID:
15690424
[PubMed - indexed for MEDLINE]
11.

High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic Arrays.

Wang J, Lin M, Crenshaw A, Hutchinson A, Hicks B, Yeager M, Berndt S, Huang WY, Hayes RB, Chanock SJ, Jones RC, Ramakrishnan R.

BMC Genomics. 2009 Nov 28;10:561. doi: 10.1186/1471-2164-10-561.

PMID:
19943955
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

Candidate SNPs for a universal individual identification panel.

Pakstis AJ, Speed WC, Kidd JR, Kidd KK.

Hum Genet. 2007 May;121(3-4):305-17. Epub 2007 Feb 27.

PMID:
17333283
[PubMed - indexed for MEDLINE]
13.

Reliability of high-throughput genotyping of whole genome amplified DNA in SNP genotyping studies.

Berthier-Schaad Y, Kao WH, Coresh J, Zhang L, Ingersoll RG, Stephens R, Smith MW.

Electrophoresis. 2007 Aug;28(16):2812-7.

PMID:
17702060
[PubMed - indexed for MEDLINE]
14.

SNPs and MALDI-TOF MS: tools for DNA typing in forensic paternity testing and anthropology.

Petkovski E, Keyser-Tracqui C, Hienne R, Ludes B.

J Forensic Sci. 2005 May;50(3):535-41.

PMID:
15932083
[PubMed - indexed for MEDLINE]
15.

Further development of multiplex single nucleotide polymorphism typing method, the DigiTag2 assay.

Nishida N, Tanabe T, Takasu M, Suyama A, Tokunaga K.

Anal Biochem. 2007 May 1;364(1):78-85. Epub 2007 Feb 13.

PMID:
17359929
[PubMed - indexed for MEDLINE]
16.

Selection of twenty-four highly informative SNP markers for human identification and paternity analysis in Koreans.

Lee HY, Park MJ, Yoo JE, Chung U, Han GR, Shin KJ.

Forensic Sci Int. 2005 Mar 10;148(2-3):107-12.

PMID:
15639604
[PubMed - indexed for MEDLINE]
17.

High fidelity of whole-genome amplified DNA on high-density single nucleotide polymorphism arrays.

Xing J, Watkins WS, Zhang Y, Witherspoon DJ, Jorde LB.

Genomics. 2008 Dec;92(6):452-6. doi: 10.1016/j.ygeno.2008.08.007. Epub 2008 Sep 27.

PMID:
18786630
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Applications of Luminex xMAP technology for rapid, high-throughput multiplexed nucleic acid detection.

Dunbar SA.

Clin Chim Acta. 2006 Jan;363(1-2):71-82. Epub 2005 Aug 15. Review.

PMID:
16102740
[PubMed - indexed for MEDLINE]
19.

Forensic validation of the SNPforID 52-plex assay.

Musgrave-Brown E, Ballard D, Balogh K, Bender K, Berger B, Bogus M, Børsting C, Brion M, Fondevila M, Harrison C, Oguzturun C, Parson W, Phillips C, Proff C, Ramos-Luis E, Sanchez JJ, Sánchez Diz P, Sobrino Rey B, Stradmann-Bellinghausen B, Thacker C, Carracedo A, Morling N, Scheithauer R, Schneider PM, Syndercombe Court D.

Forensic Sci Int Genet. 2007 Jun;1(2):186-90. doi: 10.1016/j.fsigen.2007.01.004. Epub 2007 Mar 6.

PMID:
19083753
[PubMed - indexed for MEDLINE]
20.

Selection of 29 highly informative InDel markers for human identification and paternity analysis in Chinese Han population by the SNPlex genotyping system.

Li C, Zhang S, Li L, Chen J, Liu Y, Zhao S.

Mol Biol Rep. 2012 Mar;39(3):3143-52. doi: 10.1007/s11033-011-1080-z. Epub 2011 Jun 18.

PMID:
21681421
[PubMed - indexed for MEDLINE]

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