633 related articles for article (PubMed ID: 27029637)
1. An integrated analysis tool for analyzing hybridization intensities and genotypes using new-generation population-optimized human arrays.
Huang MC; Chuang TP; Chen CH; Wu JY; Chen YT; Li LH; Yang HC
BMC Genomics; 2016 Mar; 17():266. PubMed ID: 27029637
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. SNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.
D'Amours G; Langlois M; Mathonnet G; Fetni R; Nizard S; Srour M; Tihy F; Phillips MS; Michaud JL; Lemyre E
BMC Med Genomics; 2014 Dec; 7():70. PubMed ID: 25539807
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Landscape of somatic allelic imbalances and copy number alterations in HER2-amplified breast cancer.
Staaf J; Jönsson G; Ringnér M; Baldetorp B; Borg A
Breast Cancer Res; 2011; 13(6):R129. PubMed ID: 22169037
[TBL] [Abstract][Full Text] [Related]
7. Comprehensive analysis of loss of heterozygosity events in glioblastoma using the 100K SNP mapping arrays and comparison with copy number abnormalities defined by BAC array comparative genomic hybridization.
Lo KC; Bailey D; Burkhardt T; Gardina P; Turpaz Y; Cowell JK
Genes Chromosomes Cancer; 2008 Mar; 47(3):221-37. PubMed ID: 18050302
[TBL] [Abstract][Full Text] [Related]
8. LOHAS: loss-of-heterozygosity analysis suite.
Yang HC; Chang LC; Huggins RM; Chen CH; Mullighan CG
Genet Epidemiol; 2011 May; 35(4):247-60. PubMed ID: 21312262
[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. Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans.
Haraksingh RR; Abyzov A; Urban AE
BMC Genomics; 2017 Apr; 18(1):321. PubMed ID: 28438122
[TBL] [Abstract][Full Text] [Related]
11. Detection of copy number variations in brown and white layers based on genotyping panels with different densities.
Drobik-Czwarno W; Wolc A; Fulton JE; Dekkers JCM
Genet Sel Evol; 2018 Nov; 50(1):54. PubMed ID: 30400769
[TBL] [Abstract][Full Text] [Related]
12. Clinical significance of previously cryptic copy number alterations and loss of heterozygosity in pediatric acute myeloid leukemia and myelodysplastic syndrome determined using combined array comparative genomic hybridization plus single-nucleotide polymorphism microarray analyses.
Koh KN; Lee JO; Seo EJ; Lee SW; Suh JK; Im HJ; Seo JJ
J Korean Med Sci; 2014 Jul; 29(7):926-33. PubMed ID: 25045224
[TBL] [Abstract][Full Text] [Related]
13. Genome-wide loss of heterozygosity and copy number alteration in esophageal squamous cell carcinoma using the Affymetrix GeneChip Mapping 10 K array.
Hu N; Wang C; Hu Y; Yang HH; Kong LH; Lu N; Su H; Wang QH; Goldstein AM; Buetow KH; Emmert-Buck MR; Taylor PR; Lee MP
BMC Genomics; 2006 Nov; 7():299. PubMed ID: 17134496
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. Integrated analysis of copy number and loss of heterozygosity in primary breast carcinomas using high-density SNP array.
Ching HC; Naidu R; Seong MK; Har YC; Taib NA
Int J Oncol; 2011 Sep; 39(3):621-33. PubMed ID: 21687935
[TBL] [Abstract][Full Text] [Related]
16. Use of Affymetrix Arrays in the Diagnosis of Gene Copy-Number Variation.
Zahir FR; Marra MA
Curr Protoc Hum Genet; 2015 Apr; 85():8.13.1-8.13.13. PubMed ID: 25827348
[TBL] [Abstract][Full Text] [Related]
17. MixHMM: inferring copy number variation and allelic imbalance using SNP arrays and tumor samples mixed with stromal cells.
Liu Z; Li A; Schulz V; Chen M; Tuck D
PLoS One; 2010 Jun; 5(6):e10909. PubMed ID: 20532221
[TBL] [Abstract][Full Text] [Related]
18. Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform.
Eckel-Passow JE; Atkinson EJ; Maharjan S; Kardia SL; de Andrade M
BMC Bioinformatics; 2011 May; 12():220. PubMed ID: 21627824
[TBL] [Abstract][Full Text] [Related]
19. Genome-wide detection of human copy number variations using high-density DNA oligonucleotide arrays.
Komura D; Shen F; Ishikawa S; Fitch KR; Chen W; Zhang J; Liu G; Ihara S; Nakamura H; Hurles ME; Lee C; Scherer SW; Jones KW; Shapero MH; Huang J; Aburatani H
Genome Res; 2006 Dec; 16(12):1575-84. PubMed ID: 17122084
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]