165 related articles for article (PubMed ID: 21525129)
1. Single-molecule analysis of genome rearrangements in cancer.
Pole JC; McCaughan F; Newman S; Howarth KD; Dear PH; Edwards PA
Nucleic Acids Res; 2011 Jul; 39(13):e85. PubMed ID: 21525129
[TBL] [Abstract][Full Text] [Related]
2. Deciphering the complexity of simple chromosomal insertions by genome sequencing.
Dong Z; Chau MHK; Zhang Y; Dai P; Zhu X; Leung TY; Kong X; Kwok YK; Stankiewicz P; Cheung SW; Choy KW
Hum Genet; 2021 Feb; 140(2):361-380. PubMed ID: 32728808
[TBL] [Abstract][Full Text] [Related]
3. A pipeline for complete characterization of complex germline rearrangements from long DNA reads.
Mitsuhashi S; Ohori S; Katoh K; Frith MC; Matsumoto N
Genome Med; 2020 Jul; 12(1):67. PubMed ID: 32731881
[TBL] [Abstract][Full Text] [Related]
4. Optical mapping reveals a higher level of genomic architecture of chained fusions in cancer.
Chan EKF; Cameron DL; Petersen DC; Lyons RJ; Baldi BF; Papenfuss AT; Thomas DM; Hayes VM
Genome Res; 2018 May; 28(5):726-738. PubMed ID: 29618486
[TBL] [Abstract][Full Text] [Related]
5. Whole-Genome Sequencing of Cytogenetically Balanced Chromosome Translocations Identifies Potentially Pathological Gene Disruptions and Highlights the Importance of Microhomology in the Mechanism of Formation.
Nilsson D; Pettersson M; Gustavsson P; Förster A; Hofmeister W; Wincent J; Zachariadis V; Anderlid BM; Nordgren A; Mäkitie O; Wirta V; Käller M; Vezzi F; Lupski JR; Nordenskjöld M; Lundberg ES; Carvalho CMB; Lindstrand A
Hum Mutat; 2017 Feb; 38(2):180-192. PubMed ID: 27862604
[TBL] [Abstract][Full Text] [Related]
6. Long-range massively parallel mate pair sequencing detects distinct mutations and similar patterns of structural mutability in two breast cancer cell lines.
Hampton OA; Koriabine M; Miller CA; Coarfa C; Li J; Den Hollander P; Schoenherr C; Carbone L; Nefedov M; Ten Hallers BF; Lee AV; De Jong PJ; Milosavljevic A
Cancer Genet; 2011 Aug; 204(8):447-57. PubMed ID: 21962895
[TBL] [Abstract][Full Text] [Related]
7. Identification of copy number variations and translocations in cancer cells from Hi-C data.
Chakraborty A; Ay F
Bioinformatics; 2018 Jan; 34(2):338-345. PubMed ID: 29048467
[TBL] [Abstract][Full Text] [Related]
8. Hi-C as a tool for precise detection and characterisation of chromosomal rearrangements and copy number variation in human tumours.
Harewood L; Kishore K; Eldridge MD; Wingett S; Pearson D; Schoenfelder S; Collins VP; Fraser P
Genome Biol; 2017 Jun; 18(1):125. PubMed ID: 28655341
[TBL] [Abstract][Full Text] [Related]
9. Analyses of breakpoint junctions of complex genomic rearrangements comprising multiple consecutive microdeletions by nanopore sequencing.
Imaizumi T; Yamamoto-Shimojima K; Yanagishita T; Ondo Y; Yamamoto T
J Hum Genet; 2020 Sep; 65(9):735-741. PubMed ID: 32355308
[TBL] [Abstract][Full Text] [Related]
10. Translocation and gross deletion breakpoints in human inherited disease and cancer II: Potential involvement of repetitive sequence elements in secondary structure formation between DNA ends.
Chuzhanova N; Abeysinghe SS; Krawczak M; Cooper DN
Hum Mutat; 2003 Sep; 22(3):245-51. PubMed ID: 12938089
[TBL] [Abstract][Full Text] [Related]
11. Translocation breakpoint mapping and sequence analysis in three monosomy 1p36 subjects with der(1)t(1;1)(p36;q44) suggest mechanisms for telomere capture in stabilizing de novo terminal rearrangements.
Ballif BC; Wakui K; Gajecka M; Shaffer LG
Hum Genet; 2004 Jan; 114(2):198-206. PubMed ID: 14579147
[TBL] [Abstract][Full Text] [Related]
12. High-resolution identification of balanced and complex chromosomal rearrangements by 4C technology.
Simonis M; Klous P; Homminga I; Galjaard RJ; Rijkers EJ; Grosveld F; Meijerink JP; de Laat W
Nat Methods; 2009 Nov; 6(11):837-42. PubMed ID: 19820713
[TBL] [Abstract][Full Text] [Related]
13. Chromosome segregation errors generate a diverse spectrum of simple and complex genomic rearrangements.
Ly P; Brunner SF; Shoshani O; Kim DH; Lan W; Pyntikova T; Flanagan AM; Behjati S; Page DC; Campbell PJ; Cleveland DW
Nat Genet; 2019 Apr; 51(4):705-715. PubMed ID: 30833795
[TBL] [Abstract][Full Text] [Related]
14. Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease.
Shaw CJ; Lupski JR
Hum Mol Genet; 2004 Apr; 13 Spec No 1():R57-64. PubMed ID: 14764619
[TBL] [Abstract][Full Text] [Related]
15. Mechanisms for Complex Chromosomal Insertions.
Gu S; Szafranski P; Akdemir ZC; Yuan B; Cooper ML; Magriñá MA; Bacino CA; Lalani SR; Breman AM; Smith JL; Patel A; Song RH; Bi W; Cheung SW; Carvalho CM; Stankiewicz P; Lupski JR
PLoS Genet; 2016 Nov; 12(11):e1006446. PubMed ID: 27880765
[TBL] [Abstract][Full Text] [Related]
16. Whole-genome sequencing reveals complex chromosome rearrangement disrupting NIPBL in infant with Cornelia de Lange syndrome.
Plesser Duvdevani M; Pettersson M; Eisfeldt J; Avraham O; Dagan J; Frumkin A; Lupski JR; Lindstrand A; Harel T
Am J Med Genet A; 2020 May; 182(5):1143-1151. PubMed ID: 32125084
[TBL] [Abstract][Full Text] [Related]
17. Defining the limits of detection for chromosome rearrangements in the preimplantation embryo using next generation sequencing.
Cuman C; Beyer CE; Brodie D; Fullston T; Lin JI; Willats E; Zander-Fox D; Mullen J
Hum Reprod; 2018 Aug; 33(8):1566-1576. PubMed ID: 30007310
[TBL] [Abstract][Full Text] [Related]
18. Regional assignment of six polymorphic DNA sequences on chromosome 21 by in situ hybridization to normal and rearranged chromosomes.
Münke M; Foellmer B; Watkins PC; Cowan JM; Carroll AJ; Gusella JF; Francke U
Am J Hum Genet; 1988 Apr; 42(4):542-9. PubMed ID: 3348217
[TBL] [Abstract][Full Text] [Related]
19. Copy number variant analysis using genome-wide mate-pair sequencing.
Smadbeck JB; Johnson SH; Smoley SA; Gaitatzes A; Drucker TM; Zenka RM; Kosari F; Murphy SJ; Hoppman N; Aypar U; Sukov WR; Jenkins RB; Kearney HM; Feldman AL; Vasmatzis G
Genes Chromosomes Cancer; 2018 Sep; 57(9):459-470. PubMed ID: 29726617
[TBL] [Abstract][Full Text] [Related]
20. Rapid high-resolution mapping of balanced chromosomal rearrangements on tiling CGH arrays.
Greisman HA; Hoffman NG; Yi HS
J Mol Diagn; 2011 Nov; 13(6):621-33. PubMed ID: 21907824
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
