These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

129 related articles for article (PubMed ID: 38186038)

  • 1. Low-level point heteroplasmy detection in human mitogenomes amplified with different polymerases and sequenced on MiSeq FGx platform.
    Skonieczna K; Ciesielka M; Teresiński G; Grzybowski T
    Arch Med Sadowej Kryminol; 2023; 73(2):131-138. PubMed ID: 38186038
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The effect of library preparation protocol on the efficiency of heteroplasmy detection in mitochondrial DNA using two massively parallel sequencing Illumina systems.
    Daca-Roszak P; Fiedorowicz J; Jankowski M; Ciesielka M; Teresiński G; Lipska-Zietkiewicz B; Zietkiewicz E; Grzybowski T; Skonieczna K
    J Appl Genet; 2024 Sep; 65(3):559-563. PubMed ID: 38110828
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Capability of the iSeq 100 sequencing system from Illumina to detect low-level substitutions in the human mitochondrial genome.
    Skonieczna K; Grzybowski T
    Forensic Sci Int Genet; 2023 Sep; 66():102912. PubMed ID: 37451073
    [TBL] [Abstract][Full Text] [Related]  

  • 4. MPS analysis of the mtDNA hypervariable regions on the MiSeq with improved enrichment.
    Holland MM; Wilson LA; Copeland S; Dimick G; Holland CA; Bever R; McElhoe JA
    Int J Legal Med; 2017 Jul; 131(4):919-931. PubMed ID: 28078444
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Comparison of whole mitochondrial genome variants between hair shafts and reference samples using massively parallel sequencing.
    Kim BM; Hong SR; Chun H; Kim S; Shin KJ
    Int J Legal Med; 2020 May; 134(3):853-861. PubMed ID: 31734723
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Sensitivity of mitochondrial DNA heteroplasmy detection using Next Generation Sequencing.
    González MDM; Ramos A; Aluja MP; Santos C
    Mitochondrion; 2020 Jan; 50():88-93. PubMed ID: 31669622
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mitochondrial genome sequencing with short overlapping amplicons on MiSeq FGx system.
    Xin Y; Jia R; Zhang S; Guo F
    Forensic Sci Res; 2022; 7(2):142-153. PubMed ID: 35784421
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Damage patterns observed in mtDNA control region MPS data for a range of template concentrations and when using different amplification approaches.
    Holland CA; McElhoe JA; Gaston-Sanchez S; Holland MM
    Int J Legal Med; 2021 Jan; 135(1):91-106. PubMed ID: 32940843
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Analyzing Low-Level mtDNA Heteroplasmy-Pitfalls and Challenges from Bench to Benchmarking.
    Fazzini F; Fendt L; Schönherr S; Forer L; Schöpf B; Streiter G; Losso JL; Kloss-Brandstätter A; Kronenberg F; Weissensteiner H
    Int J Mol Sci; 2021 Jan; 22(2):. PubMed ID: 33477827
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mitochondrial DNA heteroplasmy in the emerging field of massively parallel sequencing.
    Just RS; Irwin JA; Parson W
    Forensic Sci Int Genet; 2015 Sep; 18():131-9. PubMed ID: 26009256
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Human Mitochondrial Control Region and mtGenome: Design and Forensic Validation of NGS Multiplexes, Sequencing and Analytical Software.
    Holt CL; Stephens KM; Walichiewicz P; Fleming KD; Forouzmand E; Wu SF
    Genes (Basel); 2021 Apr; 12(4):. PubMed ID: 33921728
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Reducing the Number of Mismatches between Hairs and Buccal References When Analysing mtDNA Heteroplasmic Variation by Massively Parallel Sequencing.
    Gaag KJV; Desmyter S; Smit S; Prieto L; Sijen T
    Genes (Basel); 2020 Nov; 11(11):. PubMed ID: 33207560
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Whole Mitochondrial Genome Detection and Analysis of Two- to Four-Generation Maternal Pedigrees Using a New Massively Parallel Sequencing Panel.
    Peng D; Geng J; Yang J; Liu J; Wang N; Wu R; Sun H
    Genes (Basel); 2023 Apr; 14(4):. PubMed ID: 37107670
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Evaluation of the precision ID mtDNA whole genome panel on two massively parallel sequencing systems.
    Woerner AE; Ambers A; Wendt FR; King JL; Moura-Neto RS; Silva R; Budowle B
    Forensic Sci Int Genet; 2018 Sep; 36():213-224. PubMed ID: 30059903
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Development and assessment of an optimized next-generation DNA sequencing approach for the mtgenome using the Illumina MiSeq.
    McElhoe JA; Holland MM; Makova KD; Su MS; Paul IM; Baker CH; Faith SA; Young B
    Forensic Sci Int Genet; 2014 Nov; 13():20-9. PubMed ID: 25051226
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Detecting heteroplasmy from high-throughput sequencing of complete human mitochondrial DNA genomes.
    Li M; Schönberg A; Schaefer M; Schroeder R; Nasidze I; Stoneking M
    Am J Hum Genet; 2010 Aug; 87(2):237-49. PubMed ID: 20696290
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Assessment of mitochondrial DNA heteroplasmy detected on commercial panel using MPS system with artificial mixture samples.
    Cho S; Kim MY; Lee JH; Lee SD
    Int J Legal Med; 2018 Jul; 132(4):1049-1056. PubMed ID: 29279961
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Assessing heteroplasmic variant drift in the mtDNA control region of human hairs using an MPS approach.
    Gallimore JM; McElhoe JA; Holland MM
    Forensic Sci Int Genet; 2018 Jan; 32():7-17. PubMed ID: 29024924
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exploring statistical weight estimates for mitochondrial DNA matches involving heteroplasmy.
    McElhoe JA; Wilton PR; Parson W; Holland MM
    Int J Legal Med; 2022 May; 136(3):671-685. PubMed ID: 35243529
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.