Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 83

1.

A high-resolution survey of deletion polymorphism in the human genome.

Conrad DF, Andrews TD, Carter NP, Hurles ME, Pritchard JK.

Nat Genet. 2006 Jan;38(1):75-81. Epub 2005 Dec 4.

PMID:
16327808
2.

Common deletion polymorphisms in the human genome.

McCarroll SA, Hadnott TN, Perry GH, Sabeti PC, Zody MC, Barrett JC, Dallaire S, Gabriel SB, Lee C, Daly MJ, Altshuler DM; International HapMap Consortium.

Nat Genet. 2006 Jan;38(1):86-92.

PMID:
16468122
3.

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome.

Locke DP, Sharp AJ, McCarroll SA, McGrath SD, Newman TL, Cheng Z, Schwartz S, Albertson DG, Pinkel D, Altshuler DM, Eichler EE.

Am J Hum Genet. 2006 Aug;79(2):275-90. Epub 2006 Jun 15.

4.

Common deletions and SNPs are in linkage disequilibrium in the human genome.

Hinds DA, Kloek AP, Jen M, Chen X, Frazer KA.

Nat Genet. 2006 Jan;38(1):82-5. Epub 2005 Dec 4.

PMID:
16327809
5.

Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling.

Lin CH, Huang MC, Li LH, Wu JY, Chen YT, Fann CS.

Hum Mutat. 2008 Aug;29(8):1055-62. doi: 10.1002/humu.20760.

PMID:
18470944
6.

Detection of genome-wide polymorphisms in the AT-rich Plasmodium falciparum genome using a high-density microarray.

Jiang H, Yi M, Mu J, Zhang L, Ivens A, Klimczak LJ, Huyen Y, Stephens RM, Su XZ.

BMC Genomics. 2008 Aug 25;9:398. doi: 10.1186/1471-2164-9-398.

7.

High-resolution array copy number analyses for detection of deletion, gain, amplification and copy-neutral LOH in primary neuroblastoma tumors: four cases of homozygous deletions of the CDKN2A gene.

Carén H, Erichsen J, Olsson L, Enerbäck C, Sjöberg RM, Abrahamsson J, Kogner P, Martinsson T.

BMC Genomics. 2008 Jul 29;9:353. doi: 10.1186/1471-2164-9-353.

8.

High-resolution mapping of DNA copy alterations in human chromosome 22 using high-density tiling oligonucleotide arrays.

Urban AE, Korbel JO, Selzer R, Richmond T, Hacker A, Popescu GV, Cubells JF, Green R, Emanuel BS, Gerstein MB, Weissman SM, Snyder M.

Proc Natl Acad Sci U S A. 2006 Mar 21;103(12):4534-9. Epub 2006 Mar 14.

9.

SNP@Evolution: a hierarchical database of positive selection on the human genome.

Cheng F, Chen W, Richards E, Deng L, Zeng C.

BMC Evol Biol. 2009 Sep 5;9:221. doi: 10.1186/1471-2148-9-221.

10.

CGHScan: finding variable regions using high-density microarray comparative genomic hybridization data.

Anderson BD, Gilson MC, Scott AA, Biehl BS, Glasner JD, Rajashekara G, Splitter GA, Perna NT.

BMC Genomics. 2006 Apr 25;7:91.

11.

Combined array-comparative genomic hybridization and single-nucleotide polymorphism-loss of heterozygosity analysis reveals complex genetic alterations in cervical cancer.

Kloth JN, Oosting J, van Wezel T, Szuhai K, Knijnenburg J, Gorter A, Kenter GG, Fleuren GJ, Jordanova ES.

BMC Genomics. 2007 Feb 20;8:53.

12.

High-resolution genomic copy number profiling of glioblastoma multiforme by single nucleotide polymorphism DNA microarray.

Yin D, Ogawa S, Kawamata N, Tunici P, Finocchiaro G, Eoli M, Ruckert C, Huynh T, Liu G, Kato M, Sanada M, Jauch A, Dugas M, Black KL, Koeffler HP.

Mol Cancer Res. 2009 May;7(5):665-77. doi: 10.1158/1541-7786.MCR-08-0270. Epub 2009 May 12.

13.

Genetic associations of common deletion polymorphisms in families with Avellino corneal dystrophy.

Park M, Kim DJ, Kim KJ, Hong CB, Kim YJ, Cheong HS, Shin HD, Lee EJ, Kim HN, Chung HW, Kim EK, Lee JY, Kim HL.

Biochem Biophys Res Commun. 2009 Oct 2;387(4):688-93. doi: 10.1016/j.bbrc.2009.07.084. Epub 2009 Jul 19.

PMID:
19622345
14.

A new approach for using genome scans to detect recent positive selection in the human genome.

Tang K, Thornton KR, Stoneking M.

PLoS Biol. 2007 Jul;5(7):e171. Epub 2007 Jun 19.

15.

Visualization of uniparental inheritance, Mendelian inconsistencies, deletions, and parent of origin effects in single nucleotide polymorphism trio data with SNPtrio.

Ting JC, Roberson ED, Miller ND, Lysholm-Bernacchi A, Stephan DA, Capone GT, Ruczinski I, Thomas GH, Pevsner J.

Hum Mutat. 2007 Dec;28(12):1225-35.

PMID:
17661425
16.

Estimating the number of unseen variants in the human genome.

Ionita-Laza I, Lange C, M Laird N.

Proc Natl Acad Sci U S A. 2009 Mar 31;106(13):5008-13. doi: 10.1073/pnas.0807815106. Epub 2009 Mar 10.

17.

Toward accurate high-throughput SNP genotyping in the presence of inherited copy number variation.

Macconaill LE, Aldred MA, Lu X, Laframboise T.

BMC Genomics. 2007 Jul 3;8:211.

18.

Analysis and visualization of chromosomal abnormalities in SNP data with SNPscan.

Ting JC, Ye Y, Thomas GH, Ruczinski I, Pevsner J.

BMC Bioinformatics. 2006 Jan 18;7:25.

19.

Long contiguous stretches of homozygosity in the human genome.

Li LH, Ho SF, Chen CH, Wei CY, Wong WC, Li LY, Hung SI, Chung WH, Pan WH, Lee MT, Tsai FJ, Chang CF, Wu JY, Chen YT.

Hum Mutat. 2006 Nov;27(11):1115-21.

PMID:
16955415
Items per page

Supplemental Content

Write to the Help Desk