136 related articles for article (PubMed ID: 31728972)
1. Validating Gene Fusion as the Source of Chimeric RNAs.
Gupta SK; Jea JD; Yen L
Methods Mol Biol; 2020; 2079():187-207. PubMed ID: 31728972
[TBL] [Abstract][Full Text] [Related]
2. Chimeric RNAs generated by intergenic splicing in normal and cancer cells.
Jividen K; Li H
Genes Chromosomes Cancer; 2014 Dec; 53(12):963-71. PubMed ID: 25131334
[TBL] [Abstract][Full Text] [Related]
3. Identification of novel fusion genes in lung cancer using breakpoint assembly of transcriptome sequencing data.
Fernandez-Cuesta L; Sun R; Menon R; George J; Lorenz S; Meza-Zepeda LA; Peifer M; Plenker D; Heuckmann JM; Leenders F; Zander T; Dahmen I; Koker M; Schöttle J; Ullrich RT; Altmüller J; Becker C; Nürnberg P; Seidel H; Böhm D; Göke F; Ansén S; Russell PA; Wright GM; Wainer Z; Solomon B; Petersen I; Clement JH; Sänger J; Brustugun OT; Helland Å; Solberg S; Lund-Iversen M; Buettner R; Wolf J; Brambilla E; Vingron M; Perner S; Haas SA; Thomas RK
Genome Biol; 2015 Jan; 16(1):7. PubMed ID: 25650807
[TBL] [Abstract][Full Text] [Related]
4. Next generation mapping reveals novel large genomic rearrangements in prostate cancer.
Jaratlerdsiri W; Chan EKF; Petersen DC; Yang C; Croucher PI; Bornman MSR; Sheth P; Hayes VM
Oncotarget; 2017 Apr; 8(14):23588-23602. PubMed ID: 28423598
[TBL] [Abstract][Full Text] [Related]
5. Next-generation sequencing of duplication CNVs reveals that most are tandem and some create fusion genes at breakpoints.
Newman S; Hermetz KE; Weckselblatt B; Rudd MK
Am J Hum Genet; 2015 Feb; 96(2):208-20. PubMed ID: 25640679
[TBL] [Abstract][Full Text] [Related]
6. FUSIM: a software tool for simulating fusion transcripts.
Bruno AE; Miecznikowski JC; Qin M; Wang J; Liu S
BMC Bioinformatics; 2013 Jan; 14():13. PubMed ID: 23323884
[TBL] [Abstract][Full Text] [Related]
7. Breakpoint mapping by next generation sequencing reveals causative gene disruption in patients carrying apparently balanced chromosome rearrangements with intellectual deficiency and/or congenital malformations.
Schluth-Bolard C; Labalme A; Cordier MP; Till M; Nadeau G; Tevissen H; Lesca G; Boutry-Kryza N; Rossignol S; Rocas D; Dubruc E; Edery P; Sanlaville D
J Med Genet; 2013 Mar; 50(3):144-50. PubMed ID: 23315544
[TBL] [Abstract][Full Text] [Related]
8. Next-generation sequencing, FISH mapping and synteny-based modeling reveal mechanisms of decreasing dysploidy in Cucumis.
Yang L; Koo DH; Li D; Zhang T; Jiang J; Luan F; Renner SS; Hénaff E; Sanseverino W; Garcia-Mas J; Casacuberta J; Senalik DA; Simon PW; Chen J; Weng Y
Plant J; 2014 Jan; 77(1):16-30. PubMed ID: 24127692
[TBL] [Abstract][Full Text] [Related]
9. Chimeric RNAs in cancer.
Shi X; Singh S; Lin E; Li H
Adv Clin Chem; 2021; 100():1-35. PubMed ID: 33453863
[TBL] [Abstract][Full Text] [Related]
10. Transcriptome Sequencing for the Detection of Chimeric Transcripts.
Chu HT
Methods Mol Biol; 2016; 1381():239-53. PubMed ID: 26667465
[TBL] [Abstract][Full Text] [Related]
11. Identification of complex genomic breakpoint junctions in the t(9;11) MLL-AF9 fusion gene in acute leukemia.
Super HG; Strissel PL; Sobulo OM; Burian D; Reshmi SC; Roe B; Zeleznik-Le NJ; Diaz MO; Rowley JD
Genes Chromosomes Cancer; 1997 Oct; 20(2):185-95. PubMed ID: 9331569
[TBL] [Abstract][Full Text] [Related]
12. Identification of Chimeric RNAs Using RNA-Seq Reads and Protein-Protein Interactions of Translated Chimeras.
Frenkel-Morgenstern M
Methods Mol Biol; 2020; 2079():27-40. PubMed ID: 31728960
[TBL] [Abstract][Full Text] [Related]
13. Comrad: detection of expressed rearrangements by integrated analysis of RNA-Seq and low coverage genome sequence data.
McPherson A; Wu C; Hajirasouliha I; Hormozdiari F; Hach F; Lapuk A; Volik S; Shah S; Collins C; Sahinalp SC
Bioinformatics; 2011 Jun; 27(11):1481-8. PubMed ID: 21478487
[TBL] [Abstract][Full Text] [Related]
14. Intergenically Spliced Chimeric RNAs in Cancer.
Jia Y; Xie Z; Li H
Trends Cancer; 2016 Sep; 2(9):475-484. PubMed ID: 28210711
[TBL] [Abstract][Full Text] [Related]
15. Identification of the cross-strand chimeric RNAs generated by fusions of bi-directional transcripts.
Wang Y; Zou Q; Li F; Zhao W; Xu H; Zhang W; Deng H; Yang X
Nat Commun; 2021 Jul; 12(1):4645. PubMed ID: 34330918
[TBL] [Abstract][Full Text] [Related]
16. Comparison of Molecular Testing Modalities for Detection of ROS1 Rearrangements in a Cohort of Positive Patient Samples.
Davies KD; Le AT; Sheren J; Nijmeh H; Gowan K; Jones KL; Varella-Garcia M; Aisner DL; Doebele RC
J Thorac Oncol; 2018 Oct; 13(10):1474-1482. PubMed ID: 29935306
[TBL] [Abstract][Full Text] [Related]
17. RNA-mediated gene fusion in mammalian cells.
Gupta SK; Luo L; Yen L
Proc Natl Acad Sci U S A; 2018 Dec; 115(52):E12295-E12304. PubMed ID: 30538195
[TBL] [Abstract][Full Text] [Related]
18. Molecular characterization of ring chromosome 18 by low-coverage next generation sequencing.
Ji X; Liang D; Sun R; Liu C; Ma D; Wang Y; Hu P; Xu Z
BMC Med Genet; 2015 Jul; 16():57. PubMed ID: 26224010
[TBL] [Abstract][Full Text] [Related]
19. Chimeric RNAs Discovered by RNA Sequencing and Their Roles in Cancer and Rare Genetic Diseases.
Sun Y; Li H
Genes (Basel); 2022 Apr; 13(5):. PubMed ID: 35627126
[TBL] [Abstract][Full Text] [Related]
20. Sequential combination of karyotyping and RNA-sequencing in the search for cancer-specific fusion genes.
Panagopoulos I; Thorsen J; Gorunova L; Micci F; Heim S
Int J Biochem Cell Biol; 2014 Aug; 53():462-5. PubMed ID: 24863361
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
