111 related articles for article (PubMed ID: 29062110)
21. Detection of false positive mutations in BRCA gene by next generation sequencing.
Suryavanshi M; Kumar D; Panigrahi MK; Chowdhary M; Mehta A
Fam Cancer; 2017 Jul; 16(3):311-317. PubMed ID: 27848044
[TBL] [Abstract][Full Text] [Related]
22. New library construction method for single-cell genomes.
Xi L; Belyaev A; Spurgeon S; Wang X; Gong H; Aboukhalil R; Fekete R
PLoS One; 2017; 12(7):e0181163. PubMed ID: 28723968
[TBL] [Abstract][Full Text] [Related]
23. [Screening for K-ras mutations in colorectal and lung cancers by using a novel real-time PCR with ADx-K-ras kit and Sanger DNA sequencing].
Zhang HP; Fu L; Chen PQ; Ye YB; Ji TH; Zheng LM
Zhonghua Bing Li Xue Za Zhi; 2010 Nov; 39(11):757-61. PubMed ID: 21215167
[TBL] [Abstract][Full Text] [Related]
24. Performance evaluation of the next-generation sequencing approach for molecular diagnosis of hereditary hearing loss.
Sivakumaran TA; Husami A; Kissell D; Zhang W; Keddache M; Black AP; Tinkle BT; Greinwald JH; Zhang K
Otolaryngol Head Neck Surg; 2013 Jun; 148(6):1007-16. PubMed ID: 23525850
[TBL] [Abstract][Full Text] [Related]
25. Comparison of next-generation sequencing and mutation-specific platforms in clinical practice.
Hinrichs JW; van Blokland WT; Moons MJ; Radersma RD; Radersma-van Loon JH; de Voijs CM; Rappel SB; Koudijs MJ; Besselink NJ; Willems SM; de Weger RA
Am J Clin Pathol; 2015 Apr; 143(4):573-8. PubMed ID: 25780010
[TBL] [Abstract][Full Text] [Related]
26. OutLyzer: software for extracting low-allele-frequency tumor mutations from sequencing background noise in clinical practice.
Muller E; Goardon N; Brault B; Rousselin A; Paimparay G; Legros A; Fouillet R; Bruet O; Tranchant A; Domin F; San C; Quesnelle C; Frebourg T; Ricou A; Krieger S; Vaur D; Castera L
Oncotarget; 2016 Nov; 7(48):79485-79493. PubMed ID: 27825131
[TBL] [Abstract][Full Text] [Related]
27. Development of High-Throughput Clinical Testing of RPGR ORF15 Using a Large Inherited Retinal Dystrophy Cohort.
Chiang JPW; Lamey TM; Wang NK; Duan J; Zhou W; McLaren TL; Thompson JA; Ruddle J; De Roach JN
Invest Ophthalmol Vis Sci; 2018 Sep; 59(11):4434-4440. PubMed ID: 30193314
[TBL] [Abstract][Full Text] [Related]
28. Aligning to the sample-specific reference sequence to optimize the accuracy of next-generation sequencing analysis for hepatitis B virus.
Liu WC; Lin CP; Cheng CP; Ho CH; Lan KL; Cheng JH; Yen CJ; Cheng PN; Wu IC; Li IC; Chang BC; Tseng VS; Chiu YC; Chang TT
Hepatol Int; 2016 Jan; 10(1):147-57. PubMed ID: 26208819
[TBL] [Abstract][Full Text] [Related]
29. Clinical molecular testing for ASXL1 c.1934dupG p.Gly646fs mutation in hematologic neoplasms in the NGS era.
Montes-Moreno S; Routbort MJ; Lohman EJ; Barkoh BA; Kanagal-Shamanna R; Bueso-Ramos CE; Singh RR; Medeiros LJ; Luthra R; Patel KP
PLoS One; 2018; 13(9):e0204218. PubMed ID: 30222780
[TBL] [Abstract][Full Text] [Related]
30. Rapid identification and recovery of ENU-induced mutations with next-generation sequencing and Paired-End Low-Error analysis.
Pan L; Shah AN; Phelps IG; Doherty D; Johnson EA; Moens CB
BMC Genomics; 2015 Feb; 16(1):83. PubMed ID: 25886285
[TBL] [Abstract][Full Text] [Related]
31. Detection of Rare Mutations in EGFR-ARMS-PCR-Negative Lung Adenocarcinoma by Sanger Sequencing.
Liang C; Wu Z; Gan X; Liu Y; You Y; Liu C; Zhou C; Liang Y; Mo H; Chen AM; Zhang J
Yonsei Med J; 2018 Jan; 59(1):13-19. PubMed ID: 29214771
[TBL] [Abstract][Full Text] [Related]
32. A Pipeline for ctDNA Detection Following Primary Tumor Profiling Using a Cancer-Related Gene Sequencing Panel.
Nishizuka SS; Sato KA; Hachiya T
Methods Mol Biol; 2019; 1908():229-241. PubMed ID: 30649732
[TBL] [Abstract][Full Text] [Related]
33. High-fidelity target sequencing of individual molecules identified using barcode sequences: de novo detection and absolute quantitation of mutations in plasma cell-free DNA from cancer patients.
Kukita Y; Matoba R; Uchida J; Hamakawa T; Doki Y; Imamura F; Kato K
DNA Res; 2015 Aug; 22(4):269-77. PubMed ID: 26126624
[TBL] [Abstract][Full Text] [Related]
34. Hidden mutations in Cornelia de Lange syndrome limitations of sanger sequencing in molecular diagnostics.
Braunholz D; Obieglo C; Parenti I; Pozojevic J; Eckhold J; Reiz B; Braenne I; Wendt KS; Watrin E; Vodopiutz J; Rieder H; Gillessen-Kaesbach G; Kaiser FJ
Hum Mutat; 2015 Jan; 36(1):26-9. PubMed ID: 25196272
[TBL] [Abstract][Full Text] [Related]
35. [Quality evaluation and clinical applicability of pyrosequencing assay kit for detecting hepatitis B virus resistance].
Chen J; Liu Y; Zheng Z; Shen S; Sui S; Chen H; Zhou B; Sun J
Zhonghua Gan Zang Bing Za Zhi; 2015 Jun; 23(6):422-7. PubMed ID: 26236927
[TBL] [Abstract][Full Text] [Related]
36. A labor and cost effective next generation sequencing of PKHD1 in autosomal recessive polycystic kidney disease patients.
Tavira B; Gómez J; Málaga S; Santos F; Fernández-Aracama J; Alonso B; Iglesias S; Benavides A; Hernando I; Plasencia A; Alvarez V; Coto E
Gene; 2015 Apr; 561(1):165-9. PubMed ID: 25701400
[TBL] [Abstract][Full Text] [Related]
37. A Method for Next-Generation Sequencing of Paired Diagnostic and Remission Samples to Detect Mitochondrial DNA Mutations Associated with Leukemia.
Pagani IS; Kok CH; Saunders VA; Van der Hoek MB; Heatley SL; Schwarer AP; Hahn CN; Hughes TP; White DL; Ross DM
J Mol Diagn; 2017 Sep; 19(5):711-721. PubMed ID: 28732215
[TBL] [Abstract][Full Text] [Related]
38. Fast clinical molecular diagnosis of hyperphenylalaninemia using next-generation sequencing-based on a custom AmpliSeq™ panel and Ion Torrent PGM sequencing.
Cao YY; Qu YJ; Song F; Zhang T; Bai JL; Jin YW; Wang H
Mol Genet Metab; 2014 Dec; 113(4):261-6. PubMed ID: 25456745
[TBL] [Abstract][Full Text] [Related]
39. Ultrasensitive single-genome sequencing: accurate, targeted, next generation sequencing of HIV-1 RNA.
Boltz VF; Rausch J; Shao W; Hattori J; Luke B; Maldarelli F; Mellors JW; Kearney MF; Coffin JM
Retrovirology; 2016 Dec; 13(1):87. PubMed ID: 27998286
[TBL] [Abstract][Full Text] [Related]
40. KRAS gene mutation in a series of unselected colorectal carcinoma patients with prognostic morphological correlations: a pyrosequencing method improved by nested PCR.
de Macêdo MP; de Melo FM; Lisboa BC; Andrade LD; de Souza Begnami MD; Junior SA; Ribeiro HS; Soares FA; Carraro DM; da Cunha IW
Exp Mol Pathol; 2015 Jun; 98(3):563-7. PubMed ID: 25835782
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]