BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

237 related articles for article (PubMed ID: 23288206)

  • 1. Comprehensive next-generation sequence analyses of the entire mitochondrial genome reveal new insights into the molecular diagnosis of mitochondrial DNA disorders.
    Cui H; Li F; Chen D; Wang G; Truong CK; Enns GM; Graham B; Milone M; Landsverk ML; Wang J; Zhang W; Wong LJ
    Genet Med; 2013 May; 15(5):388-94. PubMed ID: 23288206
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Transition to next generation analysis of the whole mitochondrial genome: a summary of molecular defects.
    Tang S; Wang J; Zhang VW; Li FY; Landsverk M; Cui H; Truong CK; Wang G; Chen LC; Graham B; Scaglia F; Schmitt ES; Craigen WJ; Wong LJ
    Hum Mutat; 2013 Jun; 34(6):882-93. PubMed ID: 23463613
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Comprehensive one-step molecular analyses of mitochondrial genome by massively parallel sequencing.
    Zhang W; Cui H; Wong LJ
    Clin Chem; 2012 Sep; 58(9):1322-31. PubMed ID: 22777720
    [TBL] [Abstract][Full Text] [Related]  

  • 5. HiFi long-read amplicon sequencing for full-spectrum variants of human mtDNA.
    Lin Y; Wang J; Xu R; Xu Z; Wang Y; Pan S; Zhang Y; Tao Q; Zhao Y; Yan C; Cao Z; Ji K
    BMC Genomics; 2024 May; 25(1):538. PubMed ID: 38822239
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Advanced approach for comprehensive mtDNA genome testing in mitochondrial disease.
    Wang J; Balciuniene J; Diaz-Miranda MA; McCormick EM; Aref-Eshghi E; Muir AM; Cao K; Troiani J; Moseley A; Fan Z; Zolkipli-Cunningham Z; Goldstein A; Ganetzky RD; Muraresku CC; Peterson JT; Spinner NB; Wallace DC; Dulik MC; Falk MJ
    Mol Genet Metab; 2022 Jan; 135(1):93-101. PubMed ID: 34969639
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Challenges of bringing next generation sequencing technologies to clinical molecular diagnostic laboratories.
    Wong LJ
    Neurotherapeutics; 2013 Apr; 10(2):262-72. PubMed ID: 23269496
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The development of next-generation sequencing assays for the mitochondrial genome and 108 nuclear genes associated with mitochondrial disorders.
    Dames S; Chou LS; Xiao Y; Wayman T; Stocks J; Singleton M; Eilbeck K; Mao R
    J Mol Diagn; 2013 Jul; 15(4):526-34. PubMed ID: 23665194
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mitochondrial and nuclear disease panel (Mito-aND-Panel): Combined sequencing of mitochondrial and nuclear DNA by a cost-effective and sensitive NGS-based method.
    Abicht A; Scharf F; Kleinle S; Schön U; Holinski-Feder E; Horvath R; Benet-Pagès A; Diebold I
    Mol Genet Genomic Med; 2018 Nov; 6(6):1188-1198. PubMed ID: 30406974
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Targeted array CGH as a valuable molecular diagnostic approach: experience in the diagnosis of mitochondrial and metabolic disorders.
    Wang J; Zhan H; Li FY; Pursley AN; Schmitt ES; Wong LJ
    Mol Genet Metab; 2012 Jun; 106(2):221-30. PubMed ID: 22494545
    [TBL] [Abstract][Full Text] [Related]  

  • 11. MitoRS, a method for high throughput, sensitive, and accurate detection of mitochondrial DNA heteroplasmy.
    Marquis J; Lefebvre G; Kourmpetis YAI; Kassam M; Ronga F; De Marchi U; Wiederkehr A; Descombes P
    BMC Genomics; 2017 Apr; 18(1):326. PubMed ID: 28441938
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Differentiating between monozygotic twins through next-generation mitochondrial genome sequencing.
    Wang Z; Zhu R; Zhang S; Bian Y; Lu D; Li C
    Anal Biochem; 2015 Dec; 490():1-6. PubMed ID: 26327617
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Identification of the perpetrator among identical twins using next-generation sequencing technology: A case report.
    Yuan L; Chen X; Liu Z; Liu Q; Song A; Bao G; Wei G; Zhang S; Lu J; Wu Y
    Forensic Sci Int Genet; 2020 Jan; 44():102167. PubMed ID: 31605960
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Application of Genome Sequencing from Blood to Diagnose Mitochondrial Diseases.
    Rius R; Compton AG; Baker NL; Welch AE; Coman D; Kava MP; Minoche AE; Cowley MJ; Thorburn DR; Christodoulou J
    Genes (Basel); 2021 Apr; 12(4):. PubMed ID: 33924034
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Next generation molecular diagnosis of mitochondrial disorders.
    Wong LJ
    Mitochondrion; 2013 Jul; 13(4):379-87. PubMed ID: 23473862
    [TBL] [Abstract][Full Text] [Related]  

  • 16. PCR-Free Enrichment of Mitochondrial DNA from Human Blood and Cell Lines for High Quality Next-Generation DNA Sequencing.
    Gould MP; Bosworth CM; McMahon S; Grandhi S; Grimberg BT; LaFramboise T
    PLoS One; 2015; 10(10):e0139253. PubMed ID: 26488301
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The ability of human nuclear DNA to cause false positive low-abundance heteroplasmy calls varies across the mitochondrial genome.
    Albayrak L; Khanipov K; Pimenova M; Golovko G; Rojas M; Pavlidis I; Chumakov S; Aguilar G; Chávez A; Widger WR; Fofanov Y
    BMC Genomics; 2016 Dec; 17(1):1017. PubMed ID: 27955616
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Approaches to Whole Mitochondrial Genome Sequencing on the Oxford Nanopore MinION.
    Zascavage RR; Hall CL; Thorson K; Mahmoud M; Sedlazeck FJ; Planz JV
    Curr Protoc Hum Genet; 2019 Dec; 104(1):e94. PubMed ID: 31743587
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Dynamics of mitochondrial heteroplasmy in three families investigated via a repeatable re-sequencing study.
    Goto H; Dickins B; Afgan E; Paul IM; Taylor J; Makova KD; Nekrutenko A
    Genome Biol; 2011; 12(6):R59. PubMed ID: 21699709
    [TBL] [Abstract][Full Text] [Related]  

  • 20. A simple method for sequencing the whole human mitochondrial genome directly from samples and its application to genetic testing.
    Yao Y; Nishimura M; Murayama K; Kuranobu N; Tojo S; Beppu M; Ishige T; Itoga S; Tsuchida S; Mori M; Takayanagi M; Yokoyama M; Yamagata K; Kishita Y; Okazaki Y; Nomura F; Matsushita K; Tanaka T
    Sci Rep; 2019 Nov; 9(1):17411. PubMed ID: 31757988
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.