171 related articles for article (PubMed ID: 30625989)
1. Detection of Low-Frequency Mutations and Identification of Heat-Induced Artifactual Mutations Using Duplex Sequencing.
Ahn EH; Lee SH
Int J Mol Sci; 2019 Jan; 20(1):. PubMed ID: 30625989
[TBL] [Abstract][Full Text] [Related]
2. Detection of Ultra-Rare Mitochondrial Mutations in Breast Stem Cells by Duplex Sequencing.
Ahn EH; Hirohata K; Kohrn BF; Fox EJ; Chang CC; Loeb LA
PLoS One; 2015; 10(8):e0136216. PubMed ID: 26305705
[TBL] [Abstract][Full Text] [Related]
3. Detection of genome-wide low-frequency mutations with Paired-End and Complementary Consensus Sequencing (PECC-Seq) revealed end-repair-derived artifacts as residual errors.
You X; Thiruppathi S; Liu W; Cao Y; Naito M; Furihata C; Honma M; Luan Y; Suzuki T
Arch Toxicol; 2020 Oct; 94(10):3475-3485. PubMed ID: 32737516
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Detection of ultra-rare mutations by next-generation sequencing.
Schmitt MW; Kennedy SR; Salk JJ; Fox EJ; Hiatt JB; Loeb LA
Proc Natl Acad Sci U S A; 2012 Sep; 109(36):14508-13. PubMed ID: 22853953
[TBL] [Abstract][Full Text] [Related]
6. Comprehensive Mitochondrial Genome Analysis by Massively Parallel Sequencing.
Palculict ME; Zhang VW; Wong LJ; Wang J
Methods Mol Biol; 2016; 1351():3-17. PubMed ID: 26530670
[TBL] [Abstract][Full Text] [Related]
7. Discovery and characterization of artifactual mutations in deep coverage targeted capture sequencing data due to oxidative DNA damage during sample preparation.
Costello M; Pugh TJ; Fennell TJ; Stewart C; Lichtenstein L; Meldrim JC; Fostel JL; Friedrich DC; Perrin D; Dionne D; Kim S; Gabriel SB; Lander ES; Fisher S; Getz G
Nucleic Acids Res; 2013 Apr; 41(6):e67. PubMed ID: 23303777
[TBL] [Abstract][Full Text] [Related]
8. Ultra-sensitive sequencing reveals an age-related increase in somatic mitochondrial mutations that are inconsistent with oxidative damage.
Kennedy SR; Salk JJ; Schmitt MW; Loeb LA
PLoS Genet; 2013; 9(9):e1003794. PubMed ID: 24086148
[TBL] [Abstract][Full Text] [Related]
9. Next-generation sequencing methodologies to detect low-frequency mutations: "Catch me if you can".
Menon V; Brash DE
Mutat Res Rev Mutat Res; 2023; 792():108471. PubMed ID: 37716438
[TBL] [Abstract][Full Text] [Related]
10. Genome-wide direct quantification of in vivo mutagenesis using high-accuracy paired-end and complementary consensus sequencing.
You X; Cao Y; Suzuki T; Shao J; Zhu B; Masumura K; Xi J; Liu W; Zhang X; Luan Y
Nucleic Acids Res; 2023 Nov; 51(21):e109. PubMed ID: 37870450
[TBL] [Abstract][Full Text] [Related]
11. Validation of Next-Generation Sequencing of Entire Mitochondrial Genomes and the Diversity of Mitochondrial DNA Mutations in Oral Squamous Cell Carcinoma.
Kloss-Brandstätter A; Weissensteiner H; Erhart G; Schäfer G; Forer L; Schönherr S; Pacher D; Seifarth C; Stöckl A; Fendt L; Sottsas I; Klocker H; Huck CW; Rasse M; Kronenberg F; Kloss FR
PLoS One; 2015; 10(8):e0135643. PubMed ID: 26262956
[TBL] [Abstract][Full Text] [Related]
12. Direct quantification of in vivo mutagenesis and carcinogenesis using duplex sequencing.
Valentine CC; Young RR; Fielden MR; Kulkarni R; Williams LN; Li T; Minocherhomji S; Salk JJ
Proc Natl Acad Sci U S A; 2020 Dec; 117(52):33414-33425. PubMed ID: 33318186
[TBL] [Abstract][Full Text] [Related]
13. Immortalization of Different Breast Epithelial Cell Types Results in Distinct Mitochondrial Mutagenesis.
Kwon S; Kim SS; Nebeck HE; Ahn EH
Int J Mol Sci; 2019 Jun; 20(11):. PubMed ID: 31181796
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Concordance and reproducibility of a next generation mtGenome sequencing method for high-quality samples using the Illumina MiSeq.
Peck MA; Brandhagen MD; Marshall C; Diegoli TM; Irwin JA; Sturk-Andreaggi K
Forensic Sci Int Genet; 2016 Sep; 24():103-111. PubMed ID: 27368088
[TBL] [Abstract][Full Text] [Related]
17. Enhancing the accuracy of next-generation sequencing for detecting rare and subclonal mutations.
Salk JJ; Schmitt MW; Loeb LA
Nat Rev Genet; 2018 May; 19(5):269-285. PubMed ID: 29576615
[TBL] [Abstract][Full Text] [Related]
18. Application of next-generation sequencing in the detection of low-abundance mutations.
Yang L; Xin-Yue Y; Jin Y
Yi Chuan; 2024 Feb; 46(2):126-139. PubMed ID: 38340003
[TBL] [Abstract][Full Text] [Related]
19. Targeted single molecule mutation detection with massively parallel sequencing.
Gregory MT; Bertout JA; Ericson NG; Taylor SD; Mukherjee R; Robins HS; Drescher CW; Bielas JH
Nucleic Acids Res; 2016 Feb; 44(3):e22. PubMed ID: 26384417
[TBL] [Abstract][Full Text] [Related]
20. The stochastic nature of errors in next-generation sequencing of circulating cell-free DNA.
Nix DA; Hellwig S; Conley C; Thomas A; Fuertes CL; Hamil CL; Bhetariya PJ; Garrido-Laguna I; Marth GT; Bronner MP; Underhill HR
PLoS One; 2020; 15(2):e0229063. PubMed ID: 32084206
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
