156 related articles for article (PubMed ID: 28348108)
1. Comprehensive somatic genome alterations of urachal carcinoma.
Lee S; Lee J; Sim SH; Lee Y; Moon KC; Lee C; Park WY; Kim NK; Lee SH; Lee H
J Med Genet; 2017 Aug; 54(8):572-578. PubMed ID: 28348108
[TBL] [Abstract][Full Text] [Related]
2. Urachal Carcinoma Shares Genomic Alterations with Colorectal Carcinoma and May Respond to Epidermal Growth Factor Inhibition.
Collazo-Lorduy A; Castillo-Martin M; Wang L; Patel V; Iyer G; Jordan E; Al-Ahmadie H; Leonard I; Oh WK; Zhu J; McBride RB; Cordon-Cardo C; Solit DB; Sfakianos JP; Galsky MD
Eur Urol; 2016 Nov; 70(5):771-775. PubMed ID: 27178450
[TBL] [Abstract][Full Text] [Related]
3. Whole exome sequencing of urachal adenocarcinoma reveals recurrent NF1 mutations.
Singh H; Liu Y; Xiao X; Lin L; Kim J; Van Hummelen P; Wu CL; Bass AJ; Saylor PJ
Oncotarget; 2016 May; 7(20):29211-5. PubMed ID: 27078850
[TBL] [Abstract][Full Text] [Related]
4. Discovery of Aberrant Alteration of Genome in Colorectal Cancer by Exome Sequencing.
Liang Y; Jiang L; Zhong X; Hochwald SN; Wang Y; Huang L; Nie Q; Huang H; Xu JF
Am J Med Sci; 2019 Nov; 358(5):340-349. PubMed ID: 31445671
[TBL] [Abstract][Full Text] [Related]
5. Simultaneous Copy Number Alteration and Single-Nucleotide Variation Analysis in Matched Aqueous Humor and Tumor Samples in Children with Retinoblastoma.
Schmidt MJ; Prabakar RK; Pike S; Yellapantula V; Peng CC; Kuhn P; Hicks J; Xu L; Berry JL
Int J Mol Sci; 2023 May; 24(10):. PubMed ID: 37239954
[TBL] [Abstract][Full Text] [Related]
6. Whole genome sequencing reveals potential targets for therapy in patients with refractory KRAS mutated metastatic colorectal cancer.
Shanmugam V; Ramanathan RK; Lavender NA; Sinari S; Chadha M; Liang WS; Kurdoglu A; Izatt T; Christoforides A; Benson H; Phillips L; Baker A; Murray C; Hostetter G; Von Hoff DD; Craig DW; Carpten JD
BMC Med Genomics; 2014 Jun; 7():36. PubMed ID: 24943349
[TBL] [Abstract][Full Text] [Related]
7. Whole-genome sequencing is more powerful than whole-exome sequencing for detecting exome variants.
Belkadi A; Bolze A; Itan Y; Cobat A; Vincent QB; Antipenko A; Shang L; Boisson B; Casanova JL; Abel L
Proc Natl Acad Sci U S A; 2015 Apr; 112(17):5473-8. PubMed ID: 25827230
[TBL] [Abstract][Full Text] [Related]
8. Combined landscape of single-nucleotide variants and copy number alterations in clonal hematopoiesis.
Saiki R; Momozawa Y; Nannya Y; Nakagawa MM; Ochi Y; Yoshizato T; Terao C; Kuroda Y; Shiraishi Y; Chiba K; Tanaka H; Niida A; Imoto S; Matsuda K; Morisaki T; Murakami Y; Kamatani Y; Matsuda S; Kubo M; Miyano S; Makishima H; Ogawa S
Nat Med; 2021 Jul; 27(7):1239-1249. PubMed ID: 34239136
[TBL] [Abstract][Full Text] [Related]
9. Targeted sequencing of cancer-related genes in colorectal cancer using next-generation sequencing.
Han SW; Kim HP; Shin JY; Jeong EG; Lee WC; Lee KH; Won JK; Kim TY; Oh DY; Im SA; Bang YJ; Jeong SY; Park KJ; Park JG; Kang GH; Seo JS; Kim JI; Kim TY
PLoS One; 2013; 8(5):e64271. PubMed ID: 23700467
[TBL] [Abstract][Full Text] [Related]
10. Whole-exome characterization of pancreatic neuroendocrine tumor cell lines BON-1 and QGP-1.
Vandamme T; Peeters M; Dogan F; Pauwels P; Van Assche E; Beyens M; Mortier G; Vandeweyer G; de Herder W; Van Camp G; Hofland LJ; Op de Beeck K
J Mol Endocrinol; 2015 Apr; 54(2):137-47. PubMed ID: 25612765
[TBL] [Abstract][Full Text] [Related]
11. Genomic Analysis of Localized High-Risk Prostate Cancer Circulating Tumor Cells at the Single-Cell Level.
Rangel-Pozzo A; Liu S; Wajnberg G; Wang X; Ouellette RJ; Hicks GG; Drachenberg D; Mai S
Cells; 2020 Aug; 9(8):. PubMed ID: 32784507
[TBL] [Abstract][Full Text] [Related]
12. Genomic alterations in gastric cancers discovered via whole-exome sequencing.
Zhang J; Qiu W; Liu H; Qian C; Liu D; Wang H; Hu N; Tang YT; Sun J; Shen Z
BMC Cancer; 2018 Dec; 18(1):1270. PubMed ID: 30567531
[TBL] [Abstract][Full Text] [Related]
13. Evaluation of somatic copy number estimation tools for whole-exome sequencing data.
Nam JY; Kim NK; Kim SC; Joung JG; Xi R; Lee S; Park PJ; Park WY
Brief Bioinform; 2016 Mar; 17(2):185-92. PubMed ID: 26210357
[TBL] [Abstract][Full Text] [Related]
14. A Pilot Study for the Feasibility of Exome-Sequencing in Circulating Tumor Cells Versus Single Metastatic Biopsies in Breast Cancer.
Kaur P; Campo D; Porras TB; Ring A; Lu J; Chairez Y; Su Y; Kang I; Lang JE
Int J Mol Sci; 2020 Jul; 21(14):. PubMed ID: 32650480
[TBL] [Abstract][Full Text] [Related]
15. Comparative analysis of methods for identifying somatic copy number alterations from deep sequencing data.
Alkodsi A; Louhimo R; Hautaniemi S
Brief Bioinform; 2015 Mar; 16(2):242-54. PubMed ID: 24599115
[TBL] [Abstract][Full Text] [Related]
16. Genomic landscape of extraordinary responses in metastatic breast cancer.
Lim SM; Kim E; Jung KH; Kim S; Koo JS; Kim SI; Park S; Park HS; Park BW; Cho YU; Kim JY; Paik S; Kwon NJ; Kim GM; Kim JH; Kim MH; Jeon MK; Kim S; Sohn J
Commun Biol; 2021 Apr; 4(1):449. PubMed ID: 33837242
[TBL] [Abstract][Full Text] [Related]
17. Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes.
Qi Q; Jiang Y; Zhou X; Meng H; Hao N; Chang J; Bai J; Wang C; Wang M; Guo J; Ouyang Y; Xu Z; Xiao M; Zhang VW; Liu J
Genes (Basel); 2020 Nov; 11(12):. PubMed ID: 33255631
[TBL] [Abstract][Full Text] [Related]
18. Evolution of late-stage metastatic melanoma is dominated by aneuploidy and whole genome doubling.
Vergara IA; Mintoff CP; Sandhu S; McIntosh L; Young RJ; Wong SQ; Colebatch A; Cameron DL; Kwon JL; Wolfe R; Peng A; Ellul J; Dou X; Fedele C; Boyle S; Arnau GM; Raleigh J; Hatzimihalis A; Szeto P; Mooi J; Widmer DS; Cheng PF; Amann V; Dummer R; Hayward N; Wilmott J; Scolyer RA; Cho RJ; Bowtell D; Thorne H; Alsop K; Cordner S; Woodford N; Leditschke J; O'Brien P; Dawson SJ; McArthur GA; Mann GJ; Levesque MP; Papenfuss AT; Shackleton M
Nat Commun; 2021 Mar; 12(1):1434. PubMed ID: 33664264
[TBL] [Abstract][Full Text] [Related]
19. Single-cell genome sequencing of human neurons identifies somatic point mutation and indel enrichment in regulatory elements.
Luquette LJ; Miller MB; Zhou Z; Bohrson CL; Zhao Y; Jin H; Gulhan D; Ganz J; Bizzotto S; Kirkham S; Hochepied T; Libert C; Galor A; Kim J; Lodato MA; Garaycoechea JI; Gawad C; West J; Walsh CA; Park PJ
Nat Genet; 2022 Oct; 54(10):1564-1571. PubMed ID: 36163278
[TBL] [Abstract][Full Text] [Related]
20. Targeted DNA and RNA Sequencing of Paired Urothelial and Squamous Bladder Cancers Reveals Discordant Genomic and Transcriptomic Events and Unique Therapeutic Implications.
Hovelson DH; Udager AM; McDaniel AS; Grivas P; Palmbos P; Tamura S; Lazo de la Vega L; Palapattu G; Veeneman B; El-Sawy L; Sadis SE; Morgan TM; Montgomery JS; Weizer AZ; Day KC; Neamati N; Liebert M; Keller ET; Day ML; Mehra R; Tomlins SA
Eur Urol; 2018 Dec; 74(6):741-753. PubMed ID: 30033047
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
