134 related articles for article (PubMed ID: 25005691)
1. A workflow to increase verification rate of chromosomal structural rearrangements using high-throughput next-generation sequencing.
Quek K; Nones K; Patch AM; Fink JL; Newell F; Cloonan N; Miller D; Fadlullah MZ; Kassahn K; Christ AN; Bruxner TJ; Manning S; Harliwong I; Idrisoglu S; Nourse C; Nourbakhsh E; Wani S; Steptoe A; Anderson M; Holmes O; Leonard C; Taylor D; Wood S; Xu Q; ; Wilson P; Biankin AV; Pearson JV; Waddell N; Grimmond SM
Biotechniques; 2014 Jul; 57(1):31-8. PubMed ID: 25005691
[TBL] [Abstract][Full Text] [Related]
2. Resolving Breakpoints of Chromosomal Rearrangements at the Nucleotide Level Using Sanger Sequencing.
Nalbandian K; Piña-Aguilar RE; Morton CC
Curr Protoc Hum Genet; 2020 Dec; 108(1):e107. PubMed ID: 33369263
[TBL] [Abstract][Full Text] [Related]
3. Detection of variations and identifying genomic breakpoints for large deletions in the LDLR by Ion Torrent semiconductor sequencing.
Faiz F; Allcock RJ; Hooper AJ; van Bockxmeer FM
Atherosclerosis; 2013 Oct; 230(2):249-55. PubMed ID: 24075752
[TBL] [Abstract][Full Text] [Related]
4. Characterization of complex chromosomal rearrangements by targeted capture and next-generation sequencing.
Sobreira NL; Gnanakkan V; Walsh M; Marosy B; Wohler E; Thomas G; Hoover-Fong JE; Hamosh A; Wheelan SJ; Valle D
Genome Res; 2011 Oct; 21(10):1720-7. PubMed ID: 21890680
[TBL] [Abstract][Full Text] [Related]
5. A New Next-Generation Sequencing Strategy for the Simultaneous Analysis of Mutations and Chromosomal Rearrangements at DNA Level in Acute Myeloid Leukemia Patients.
Prieto-Conde MI; Corchete LA; García-Álvarez M; Jiménez C; Medina A; Balanzategui A; Hernández-Ruano M; Maldonado R; Sarasquete ME; Alcoceba M; Puig N; González-Calle V; García-Sanz R; Gutiérrez NC; González-Díaz M; Chillón MC
J Mol Diagn; 2020 Jan; 22(1):60-71. PubMed ID: 31605801
[TBL] [Abstract][Full Text] [Related]
6. Amplification and thrifty single-molecule sequencing of recurrent somatic structural variations.
Patel A; Schwab R; Liu YT; Bafna V
Genome Res; 2014 Feb; 24(2):318-28. PubMed ID: 24307551
[TBL] [Abstract][Full Text] [Related]
7. Comparison of Next-Generation Sequencing Panels and Platforms for Detection and Verification of Somatic Tumor Variants for Clinical Diagnostics.
Misyura M; Zhang T; Sukhai MA; Thomas M; Garg S; Kamel-Reid S; Stockley TL
J Mol Diagn; 2016 Nov; 18(6):842-850. PubMed ID: 27770852
[TBL] [Abstract][Full Text] [Related]
8. Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms.
Malhotra A; Lindberg M; Faust GG; Leibowitz ML; Clark RA; Layer RM; Quinlan AR; Hall IM
Genome Res; 2013 May; 23(5):762-76. PubMed ID: 23410887
[TBL] [Abstract][Full Text] [Related]
9. Analysis of the genetic diversity of influenza A viruses using next-generation DNA sequencing.
Van den Hoecke S; Verhelst J; Vuylsteke M; Saelens X
BMC Genomics; 2015 Feb; 16(1):79. PubMed ID: 25758772
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Characterising chromosome rearrangements: recent technical advances in molecular cytogenetics.
Le Scouarnec S; Gribble SM
Heredity (Edinb); 2012 Jan; 108(1):75-85. PubMed ID: 22086080
[TBL] [Abstract][Full Text] [Related]
12. [Comparison of different massive parallel sequencing platforms for mutation profiling in formalin-fixed and paraffin-embedded samples].
Jiang RR; Wang YJ; Teng XD; Xiao L; Bu H; Ye F
Zhonghua Bing Li Xue Za Zhi; 2018 Aug; 47(8):591-596. PubMed ID: 30107663
[No Abstract] [Full Text] [Related]
13. Targeted next-generation sequencing at copy-number breakpoints for personalized analysis of rearranged ends in solid tumors.
Kim HK; Park WC; Lee KM; Hwang HL; Park SY; Sorn S; Chandra V; Kim KG; Yoon WB; Bae JS; Shin HD; Shin JY; Seoh JY; Kim JI; Hong KM
PLoS One; 2014; 9(6):e100089. PubMed ID: 24937453
[TBL] [Abstract][Full Text] [Related]
14. Application of High-Throughput Next-Generation Sequencing for HLA Typing on Buccal Extracted DNA: Results from over 10,000 Donor Recruitment Samples.
Yin Y; Lan JH; Nguyen D; Valenzuela N; Takemura P; Bolon YT; Springer B; Saito K; Zheng Y; Hague T; Pasztor A; Horvath G; Rigo K; Reed EF; Zhang Q
PLoS One; 2016; 11(10):e0165810. PubMed ID: 27798706
[TBL] [Abstract][Full Text] [Related]
15. Towards clinical molecular diagnosis of inherited cardiac conditions: a comparison of bench-top genome DNA sequencers.
Li X; Buckton AJ; Wilkinson SL; John S; Walsh R; Novotny T; Valaskova I; Gupta M; Game L; Barton PJ; Cook SA; Ware JS
PLoS One; 2013; 8(7):e67744. PubMed ID: 23861798
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Low-Cost, High-Throughput Sequencing of DNA Assemblies Using a Highly Multiplexed Nextera Process.
Shapland EB; Holmes V; Reeves CD; Sorokin E; Durot M; Platt D; Allen C; Dean J; Serber Z; Newman J; Chandran S
ACS Synth Biol; 2015 Jul; 4(7):860-6. PubMed ID: 25913499
[TBL] [Abstract][Full Text] [Related]
18. Next-generation sequencing as a tool for breakpoint analysis in rearrangements of the globin gene clusters.
Clark BE; Shooter C; Smith F; Brawand D; Thein SL
Int J Lab Hematol; 2017 May; 39 Suppl 1():111-120. PubMed ID: 28447426
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Single-Step IGHV Next-Generation Sequencing Detects Clonality and Somatic Hypermutation in Lymphoid Malignancies: A Phase III Diagnostic Accuracy Study.
Gazzola A; Navari M; Mannu C; Donelli R; Etebari M; Piccaluga PP
Cancers (Basel); 2023 Sep; 15(18):. PubMed ID: 37760593
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]