168 related articles for article (PubMed ID: 37870450)
21. Sequencing technologies and genome sequencing.
Pareek CS; Smoczynski R; Tretyn A
J Appl Genet; 2011 Nov; 52(4):413-35. PubMed ID: 21698376
[TBL] [Abstract][Full Text] [Related]
22. Library preparation methods for next-generation sequencing: tone down the bias.
van Dijk EL; Jaszczyszyn Y; Thermes C
Exp Cell Res; 2014 Mar; 322(1):12-20. PubMed ID: 24440557
[TBL] [Abstract][Full Text] [Related]
23. Pseudo-Sanger sequencing: massively parallel production of long and near error-free reads using NGS technology.
Ruan J; Jiang L; Chong Z; Gong Q; Li H; Li C; Tao Y; Zheng C; Zhai W; Turissini D; Cannon CH; Lu X; Wu CI
BMC Genomics; 2013 Oct; 14(1):711. PubMed ID: 24134808
[TBL] [Abstract][Full Text] [Related]
24. High-throughput sequencing in mutation detection: A new generation of genotoxicity tests?
Maslov AY; Quispe-Tintaya W; Gorbacheva T; White RR; Vijg J
Mutat Res; 2015 Jun; 776():136-43. PubMed ID: 25934519
[TBL] [Abstract][Full Text] [Related]
25. Targeted Single Primer Enrichment Sequencing with Single End Duplex-UMI.
Peng Q; Xu C; Kim D; Lewis M; DiCarlo J; Wang Y
Sci Rep; 2019 Mar; 9(1):4810. PubMed ID: 30886209
[TBL] [Abstract][Full Text] [Related]
26. Comparison of the transgenic rodent mutation assay, error corrected next generation duplex sequencing, and the alkaline comet assay to detect dose-related mutations following exposure to N-nitrosodiethylamine.
Bercu JP; Zhang S; Sobol Z; Escobar PA; Van P; Schuler M
Mutat Res Genet Toxicol Environ Mutagen; 2023 Oct; 891():503685. PubMed ID: 37770142
[TBL] [Abstract][Full Text] [Related]
27. Chemically induced mutations in a MutaMouse reporter gene inform mechanisms underlying human cancer mutational signatures.
Beal MA; Meier MJ; LeBlanc DP; Maurice C; O'Brien JM; Yauk CL; Marchetti F
Commun Biol; 2020 Aug; 3(1):438. PubMed ID: 32796912
[TBL] [Abstract][Full Text] [Related]
28. Ultrasensitive and high-efficiency screen of de novo low-frequency mutations by o2n-seq.
Wang K; Lai S; Yang X; Zhu T; Lu X; Wu CI; Ruan J
Nat Commun; 2017 May; 8():15335. PubMed ID: 28530222
[TBL] [Abstract][Full Text] [Related]
29. Duplex sequencing identifies genomic features that determine susceptibility to benzo(a)pyrene-induced in vivo mutations.
LeBlanc DPM; Meier M; Lo FY; Schmidt E; Valentine C; Williams A; Salk JJ; Yauk CL; Marchetti F
BMC Genomics; 2022 Jul; 23(1):542. PubMed ID: 35902794
[TBL] [Abstract][Full Text] [Related]
30. Single-strand specific nuclease enhances accuracy of error-corrected sequencing and improves rare mutation-detection sensitivity.
Otsubo Y; Matsumura S; Ikeda N; Yamane M
Arch Toxicol; 2022 Jan; 96(1):377-386. PubMed ID: 34767040
[TBL] [Abstract][Full Text] [Related]
31. Single duplex DNA sequencing with CODEC detects mutations with high sensitivity.
Bae JH; Liu R; Roberts E; Nguyen E; Tabrizi S; Rhoades J; Blewett T; Xiong K; Gydush G; Shea D; An Z; Patel S; Cheng J; Sridhar S; Liu MH; Lassen E; Skytte AB; Grońska-Pęski M; Shoag JE; Evrony GD; Parsons HA; Mayer EL; Makrigiorgos GM; Golub TR; Adalsteinsson VA
Nat Genet; 2023 May; 55(5):871-879. PubMed ID: 37106072
[TBL] [Abstract][Full Text] [Related]
32. RADAR-seq: A RAre DAmage and Repair sequencing method for detecting DNA damage on a genome-wide scale.
Zatopek KM; Potapov V; Maduzia LL; Alpaslan E; Chen L; Evans TC; Ong JL; Ettwiller LM; Gardner AF
DNA Repair (Amst); 2019 Aug; 80():36-44. PubMed ID: 31247470
[TBL] [Abstract][Full Text] [Related]
33. A high-throughput next-generation sequencing-based method for detecting the mutational fingerprint of carcinogens.
Besaratinia A; Li H; Yoon JI; Zheng A; Gao H; Tommasi S
Nucleic Acids Res; 2012 Aug; 40(15):e116. PubMed ID: 22735701
[TBL] [Abstract][Full Text] [Related]
34. Evaluation of the correctable decoding sequencing as a new powerful strategy for DNA sequencing.
Cheng C; Xiao P
Life Sci Alliance; 2022 Aug; 5(8):. PubMed ID: 35422436
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Targeted sequencing of both DNA strands barcoded and captured individually by RNA probes to identify genome-wide ultra-rare mutations.
Wang Q; Wang X; Tang PS; O'leary GM; Zhang M
Sci Rep; 2017 Jun; 7(1):3356. PubMed ID: 28611392
[TBL] [Abstract][Full Text] [Related]
37. Artifactual mutations resulting from DNA lesions limit detection levels in ultrasensitive sequencing applications.
Arbeithuber B; Makova KD; Tiemann-Boege I
DNA Res; 2016 Dec; 23(6):547-559. PubMed ID: 27477585
[TBL] [Abstract][Full Text] [Related]
38. Horizon scanning for novel and emerging in vitro mammalian cell mutagenicity test systems.
Evans SJ; Gollapudi B; Moore MM; Doak SH
Mutat Res Genet Toxicol Environ Mutagen; 2019 Nov; 847():403024. PubMed ID: 31699342
[TBL] [Abstract][Full Text] [Related]
39. CHOPER filters enable rare mutation detection in complex mutagenesis populations by next-generation sequencing.
Salehi F; Baronio R; Idrogo-Lam R; Vu H; Hall LV; Kaiser P; Lathrop RH
PLoS One; 2015; 10(2):e0116877. PubMed ID: 25692681
[TBL] [Abstract][Full Text] [Related]
40. Duplex sequencing provides detailed characterization of mutation frequencies and spectra in the bone marrow of MutaMouse males exposed to procarbazine hydrochloride.
Dodge AE; LeBlanc DPM; Zhou G; Williams A; Meier MJ; Van P; Lo FY; Valentine Iii CC; Salk JJ; Yauk CL; Marchetti F
Arch Toxicol; 2023 Aug; 97(8):2245-2259. PubMed ID: 37341741
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
