These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
189 related articles for article (PubMed ID: 31901979)
1. Genome-wide somatic copy number alteration analysis and database construction for cervical cancer. Luo H; Xu X; Yang J; Wang K; Wang C; Yang P; Cai H Mol Genet Genomics; 2020 May; 295(3):765-773. PubMed ID: 31901979 [TBL] [Abstract][Full Text] [Related]
2. Comprehensive identification and characterization of somatic copy number alterations in triple‑negative breast cancer. Li Z; Zhang X; Hou C; Zhou Y; Chen J; Cai H; Ye Y; Liu J; Huang N Int J Oncol; 2020 Feb; 56(2):522-530. PubMed ID: 31894314 [TBL] [Abstract][Full Text] [Related]
3. The Landscape of Somatic Copy Number Alterations in Head and Neck Squamous Cell Carcinoma. Yang J; Chen Y; Luo H; Cai H Front Oncol; 2020; 10():321. PubMed ID: 32226775 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Identification of driver genes regulating immune cell infiltration in cervical cancer by multiple omics integration. Wen Y; Zhang S; Yang J; Guo D Biomed Pharmacother; 2019 Dec; 120():109546. PubMed ID: 31675687 [TBL] [Abstract][Full Text] [Related]
6. CaSNP: a database for interrogating copy number alterations of cancer genome from SNP array data. Cao Q; Zhou M; Wang X; Meyer CA; Zhang Y; Chen Z; Li C; Liu XS Nucleic Acids Res; 2011 Jan; 39(Database issue):D968-74. PubMed ID: 20972221 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. MethCNA: a database for integrating genomic and epigenomic data in human cancer. Deng G; Yang J; Zhang Q; Xiao ZX; Cai H BMC Genomics; 2018 Feb; 19(1):138. PubMed ID: 29433427 [TBL] [Abstract][Full Text] [Related]
10. A systematic comparison of copy number alterations in four types of female cancer. Kaveh F; Baumbusch LO; Nebdal D; Børresen-Dale AL; Lingjærde OC; Edvardsen H; Kristensen VN; Solvang HK BMC Cancer; 2016 Nov; 16(1):913. PubMed ID: 27876019 [TBL] [Abstract][Full Text] [Related]
11. Genome-wide identification of significant aberrations in cancer genome. Yuan X; Yu G; Hou X; Shih IeM; Clarke R; Zhang J; Hoffman EP; Wang RR; Zhang Z; Wang Y BMC Genomics; 2012 Jul; 13():342. PubMed ID: 22839576 [TBL] [Abstract][Full Text] [Related]
12. ChromothripsisDB: A Curated Database for the Documentation, Visualization, and Mining of Chromothripsis Data. Cai H Methods Mol Biol; 2018; 1769():279-289. PubMed ID: 29564831 [TBL] [Abstract][Full Text] [Related]
13. Genome-wide analysis of recurrent copy-number alterations and copy-neutral loss of heterozygosity in head and neck squamous cell carcinoma. Marescalco MS; Capizzi C; Condorelli DF; Barresi V J Oral Pathol Med; 2014 Jan; 43(1):20-7. PubMed ID: 23750501 [TBL] [Abstract][Full Text] [Related]
14. Recurrent copy number alterations in prostate cancer: an in silico meta-analysis of publicly available genomic data. Williams JL; Greer PA; Squire JA Cancer Genet; 2014; 207(10-12):474-88. PubMed ID: 25434580 [TBL] [Abstract][Full Text] [Related]
16. arrayMap: a reference resource for genomic copy number imbalances in human malignancies. Cai H; Kumar N; Baudis M PLoS One; 2012; 7(5):e36944. PubMed ID: 22629346 [TBL] [Abstract][Full Text] [Related]
17. Genomic landscape of copy number aberrations enables the identification of oncogenic drivers in hepatocellular carcinoma. Wang K; Lim HY; Shi S; Lee J; Deng S; Xie T; Zhu Z; Wang Y; Pocalyko D; Yang WJ; Rejto PA; Mao M; Park CK; Xu J Hepatology; 2013 Aug; 58(2):706-17. PubMed ID: 23505090 [TBL] [Abstract][Full Text] [Related]
18. Whole Genome Pathway Analysis Identifies an Association of Cadmium Response Gene Loss with Copy Number Variation in Mutant p53 Bearing Uterine Endometrial Carcinomas. Delaney JR; Stupack DG PLoS One; 2016; 11(7):e0159114. PubMed ID: 27391266 [TBL] [Abstract][Full Text] [Related]
19. Hierarchical discovery of large-scale and focal copy number alterations in low-coverage cancer genomes. Khalil AIS; Khyriem C; Chattopadhyay A; Sanyal A BMC Bioinformatics; 2020 Apr; 21(1):147. PubMed ID: 32299346 [TBL] [Abstract][Full Text] [Related]
20. CancerTracer: a curated database for intrapatient tumor heterogeneity. Wang C; Yang J; Luo H; Wang K; Wang Y; Xiao ZX; Tao X; Jiang H; Cai H Nucleic Acids Res; 2020 Jan; 48(D1):D797-D806. PubMed ID: 31701131 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]