184 related articles for article (PubMed ID: 19775444)
1. Detection of recurrent copy number alterations in the genome: taking among-subject heterogeneity seriously.
Rueda OM; Diaz-Uriarte R
BMC Bioinformatics; 2009 Sep; 10():308. PubMed ID: 19775444
[TBL] [Abstract][Full Text] [Related]
2. Computational methods for identification of recurrent copy number alteration patterns by array CGH.
Shah SP
Cytogenet Genome Res; 2008; 123(1-4):343-51. PubMed ID: 19287173
[TBL] [Abstract][Full Text] [Related]
3. Integrated analysis of copy number alteration and RNA expression profiles of cancer using a high-resolution whole-genome oligonucleotide array.
Jung SH; Shin SH; Yim SH; Choi HS; Lee SH; Chung YJ
Exp Mol Med; 2009 Jul; 41(7):462-70. PubMed ID: 19322034
[TBL] [Abstract][Full Text] [Related]
4. Conditional random pattern model for copy number aberration detection.
Li F; Zhou X; Huang W; Chang CC; Wong ST
BMC Bioinformatics; 2010 Apr; 11():200. PubMed ID: 20412592
[TBL] [Abstract][Full Text] [Related]
5. RJaCGH: Bayesian analysis of aCGH arrays for detecting copy number changes and recurrent regions.
Rueda OM; Diaz-Uriarte R
Bioinformatics; 2009 Aug; 25(15):1959-60. PubMed ID: 19420051
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Genome complexity in acute lymphoblastic leukemia is revealed by array-based comparative genomic hybridization.
Strefford JC; Worley H; Barber K; Wright S; Stewart AR; Robinson HM; Bettney G; van Delft FW; Atherton MG; Davies T; Griffiths M; Hing S; Ross FM; Talley P; Saha V; Moorman AV; Harrison CJ
Oncogene; 2007 Jun; 26(29):4306-18. PubMed ID: 17237825
[TBL] [Abstract][Full Text] [Related]
8. Folic acid supplementation and malaria susceptibility and severity among people taking antifolate antimalarial drugs in endemic areas.
Crider K; Williams J; Qi YP; Gutman J; Yeung L; Mai C; Finkelstain J; Mehta S; Pons-Duran C; Menéndez C; Moraleda C; Rogers L; Daniels K; Green P
Cochrane Database Syst Rev; 2022 Feb; 2(2022):. PubMed ID: 36321557
[TBL] [Abstract][Full Text] [Related]
9. Modeling recurrent DNA copy number alterations in array CGH data.
Shah SP; Lam WL; Ng RT; Murphy KP
Bioinformatics; 2007 Jul; 23(13):i450-8. PubMed ID: 17646330
[TBL] [Abstract][Full Text] [Related]
10. CNApp, a tool for the quantification of copy number alterations and integrative analysis revealing clinical implications.
Franch-Expósito S; Bassaganyas L; Vila-Casadesús M; Hernández-Illán E; Esteban-Fabró R; Díaz-Gay M; Lozano JJ; Castells A; Llovet JM; Castellví-Bel S; Camps J
Elife; 2020 Jan; 9():. PubMed ID: 31939734
[TBL] [Abstract][Full Text] [Related]
11. Clonal heterogeneity in childhood myelodysplastic syndromes--challenge for the detection of chromosomal imbalances by array-CGH.
Praulich I; Tauscher M; Göhring G; Glaser S; Hofmann W; Feurstein S; Flotho C; Lichter P; Niemeyer CM; Schlegelberger B; Steinemann D
Genes Chromosomes Cancer; 2010 Oct; 49(10):885-900. PubMed ID: 20589934
[TBL] [Abstract][Full Text] [Related]
12. Novel insights into breast cancer copy number genetic heterogeneity revealed by single-cell genome sequencing.
Baslan T; Kendall J; Volyanskyy K; McNamara K; Cox H; D'Italia S; Ambrosio F; Riggs M; Rodgers L; Leotta A; Song J; Mao Y; Wu J; Shah R; Gularte-Mérida R; Chadalavada K; Nanjangud G; Varadan V; Gordon A; Curtis C; Krasnitz A; Dimitrova N; Harris L; Wigler M; Hicks J
Elife; 2020 May; 9():. PubMed ID: 32401198
[TBL] [Abstract][Full Text] [Related]
13. Interpretation of copy number alterations identified through clinical microarray-comparative genomic hybridization.
Pyatt RE; Astbury C
Clin Lab Med; 2011 Dec; 31(4):565-80, viii. PubMed ID: 22118737
[TBL] [Abstract][Full Text] [Related]
14. Integration of transcript expression, copy number and LOH analysis of infiltrating ductal carcinoma of the breast.
Hawthorn L; Luce J; Stein L; Rothschild J
BMC Cancer; 2010 Aug; 10():460. PubMed ID: 20799942
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Detection of copy number alterations in metastatic melanoma by a DNA fluorescence in situ hybridization probe panel and array comparative genomic hybridization: a southwest oncology group study (S9431).
Moore SR; Persons DL; Sosman JA; Bobadilla D; Bedell V; Smith DD; Wolman SR; Tuthill RJ; Moon J; Sondak VK; Slovak ML
Clin Cancer Res; 2008 May; 14(10):2927-35. PubMed ID: 18483359
[TBL] [Abstract][Full Text] [Related]
17. A multi-sample based method for identifying common CNVs in normal human genomic structure using high-resolution aCGH data.
Park C; Ahn J; Yoon Y; Park S
PLoS One; 2011; 6(10):e26975. PubMed ID: 22073121
[TBL] [Abstract][Full Text] [Related]
18. Genomic copy-number alterations of MYC and FHIT genes are associated with survival in esophageal squamous-cell carcinoma.
Miyawaki Y; Kawachi H; Ooi A; Eishi Y; Kawano T; Inazawa J; Imoto I
Cancer Sci; 2012 Aug; 103(8):1558-66. PubMed ID: 22578181
[TBL] [Abstract][Full Text] [Related]
19. Genome-wide comparison of paired fresh frozen and formalin-fixed paraffin-embedded gliomas by custom BAC and oligonucleotide array comparative genomic hybridization: facilitating analysis of archival gliomas.
Mohapatra G; Engler DA; Starbuck KD; Kim JC; Bernay DC; Scangas GA; Rousseau A; Batchelor TT; Betensky RA; Louis DN
Acta Neuropathol; 2011 Apr; 121(4):529-43. PubMed ID: 21080181
[TBL] [Abstract][Full Text] [Related]
20. Genomic profiling by array comparative genomic hybridization reveals novel DNA copy number changes in breast phyllodes tumours.
Kuijper A; Snijders AM; Berns EM; Kuenen-Boumeester V; van der Wall E; Albertson DG; van Diest PJ
Cell Oncol; 2009; 31(1):31-9. PubMed ID: 19096148
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
