108 related articles for article (PubMed ID: 18025694)
1. Genome-wide copy number analysis on GeneChip platform using copy number analyzer for affymetrix GeneChip 2.0 software.
Ogawa S; Nanya Y; Yamamoto G
Methods Mol Biol; 2007; 396():185-206. PubMed ID: 18025694
[TBL] [Abstract][Full Text] [Related]
2. A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays.
Nannya Y; Sanada M; Nakazaki K; Hosoya N; Wang L; Hangaishi A; Kurokawa M; Chiba S; Bailey DK; Kennedy GC; Ogawa S
Cancer Res; 2005 Jul; 65(14):6071-9. PubMed ID: 16024607
[TBL] [Abstract][Full Text] [Related]
3. [Genome-wide detection of loss of heterozygosity and copy number variation in a human lung large cell carcinoma cell line by affymetrix single-nucleotide polymorphism array 500K.].
Hu B; Chen J; Liu H; Wu H; Wu Z; Wang Y; Bai Y; Li Y; Zhou Q
Zhongguo Fei Ai Za Zhi; 2008 Jun; 11(3):327-32. PubMed ID: 20731928
[TBL] [Abstract][Full Text] [Related]
4. Single-nucleotide polymorphism array karyotyping in clinical practice: where, when, and how?
Sato-Otsubo A; Sanada M; Ogawa S
Semin Oncol; 2012 Feb; 39(1):13-25. PubMed ID: 22289488
[TBL] [Abstract][Full Text] [Related]
5. 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; 8():53. PubMed ID: 17311676
[TBL] [Abstract][Full Text] [Related]
6. Allelic imbalance analysis using a single-nucleotide polymorphism microarray for the detection of bladder cancer recurrence.
Coenen MJ; Ploeg M; Schijvenaars MM; Cornel EB; Karthaus HF; Scheffer H; Witjes JA; Franke B; Kiemeney LA
Clin Cancer Res; 2008 Dec; 14(24):8198-204. PubMed ID: 19088036
[TBL] [Abstract][Full Text] [Related]
7. 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. PubMed ID: 18470944
[TBL] [Abstract][Full Text] [Related]
8. Copy number estimation algorithms and fluorescence in situ hybridization to describe copy number alterations in human tumors.
Suzuki M; Nagura K; Igarashi H; Tao H; Midorikawa Y; Kitayama Y; Sugimura H
Pathol Int; 2009 Apr; 59(4):218-28. PubMed ID: 19351364
[TBL] [Abstract][Full Text] [Related]
9. High-resolution analysis of allelic imbalance in neuroblastoma cell lines by single nucleotide polymorphism arrays.
Carr J; Bown NP; Case MC; Hall AG; Lunec J; Tweddle DA
Cancer Genet Cytogenet; 2007 Jan; 172(2):127-38. PubMed ID: 17213021
[TBL] [Abstract][Full Text] [Related]
10. Genome-wide copy number profiling on high-density bacterial artificial chromosomes, single-nucleotide polymorphisms, and oligonucleotide microarrays: a platform comparison based on statistical power analysis.
Hehir-Kwa JY; Egmont-Petersen M; Janssen IM; Smeets D; van Kessel AG; Veltman JA
DNA Res; 2007 Feb; 14(1):1-11. PubMed ID: 17363414
[TBL] [Abstract][Full Text] [Related]
11. Genome-wide copy number alterations detection in fresh frozen and matched FFPE samples using SNP 6.0 arrays.
Tuefferd M; De Bondt A; Van Den Wyngaert I; Talloen W; Verbeke T; Carvalho B; Clevert DA; Alifano M; Raghavan N; Amaratunga D; Göhlmann H; Broët P; Camilleri-Broët S
Genes Chromosomes Cancer; 2008 Nov; 47(11):957-64. PubMed ID: 18663747
[TBL] [Abstract][Full Text] [Related]
12. A genome-wide analysis of loss of heterozygosity and chromosomal copy number variation in Proteus syndrome using high-density SNP microarrays.
Yilmaz A; Hamel N; Schwartz CE; Houlston RS; Harper JI; Foulkes WD
J Hum Genet; 2010 Sep; 55(9):627-30. PubMed ID: 20555334
[TBL] [Abstract][Full Text] [Related]
13. Screening for copy-number alterations and loss of heterozygosity in chronic lymphocytic leukemia--a comparative study of four differently designed, high resolution microarray platforms.
Gunnarsson R; Staaf J; Jansson M; Ottesen AM; Göransson H; Liljedahl U; Ralfkiaer U; Mansouri M; Buhl AM; Smedby KE; Hjalgrim H; Syvänen AC; Borg A; Isaksson A; Jurlander J; Juliusson G; Rosenquist R
Genes Chromosomes Cancer; 2008 Aug; 47(8):697-711. PubMed ID: 18484635
[TBL] [Abstract][Full Text] [Related]
14. Hot topic: performance of bovine high-density genotyping platforms in Holsteins and Jerseys.
Rincon G; Weber KL; Eenennaam AL; Golden BL; Medrano JF
J Dairy Sci; 2011 Dec; 94(12):6116-21. PubMed ID: 22118099
[TBL] [Abstract][Full Text] [Related]
15. Recent advances in array comparative genomic hybridization technologies and their applications in human genetics.
Lockwood WW; Chari R; Chi B; Lam WL
Eur J Hum Genet; 2006 Feb; 14(2):139-48. PubMed ID: 16288307
[TBL] [Abstract][Full Text] [Related]
16. Whole genome SNP arrays using DNA derived from formalin-fixed, paraffin-embedded ovarian tumor tissue.
Thompson ER; Herbert SC; Forrest SM; Campbell IG
Hum Mutat; 2005 Oct; 26(4):384-9. PubMed ID: 16116623
[TBL] [Abstract][Full Text] [Related]
17. ITALICS: an algorithm for normalization and DNA copy number calling for Affymetrix SNP arrays.
Rigaill G; Hupé P; Almeida A; La Rosa P; Meyniel JP; Decraene C; Barillot E
Bioinformatics; 2008 Mar; 24(6):768-74. PubMed ID: 18252739
[TBL] [Abstract][Full Text] [Related]
18. Noise reduction from genotyping microarrays using probe level information.
Komura D; Nishimura K; Ishikawa S; Panda B; Huang J; Nakamura H; Ihara S; Hirose M; Jones KW; Aburatani H
In Silico Biol; 2006; 6(1-2):79-92. PubMed ID: 16789916
[TBL] [Abstract][Full Text] [Related]
19. [Detection of a copy number mutation on chromosome 7q36 using the Affymetrix SNP Array 6.0].
Ma F; Wu FX; Li N; Liu Q; Yang W; Zhang X; Sun M
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Jun; 26(3):336-9. PubMed ID: 19504452
[TBL] [Abstract][Full Text] [Related]
20. TAFFYS: An Integrated Tool for Comprehensive Analysis of Genomic Aberrations in Tumor Samples.
Liu Y; Li A; Feng H; Wang M
PLoS One; 2015; 10(6):e0129835. PubMed ID: 26111017
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
