173 related articles for article (PubMed ID: 33781964)
1. Current and New Next-Generation Sequencing Approaches to Study Mitochondrial DNA.
Legati A; Zanetti N; Nasca A; Peron C; Lamperti C; Lamantea E; Ghezzi D
J Mol Diagn; 2021 Jun; 23(6):732-741. PubMed ID: 33781964
[TBL] [Abstract][Full Text] [Related]
2. Novel economical, accurate, sensitive, single-cell analytical method for mitochondrial DNA quantification in mtDNA mutation carriers.
Zou W; Zong K; Zhang Z; Shen L; Wang X; Su X; Wang X; Yin T; Liang C; Liu Y; Liang D; Hu C; Cao Y; Ji D
J Assist Reprod Genet; 2023 Sep; 40(9):2197-2209. PubMed ID: 37462790
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Oocyte mitochondrial deletions and heteroplasmy in a bovine model of ageing and ovarian stimulation.
Hammond ER; Green MP; Shelling AN; Berg MC; Peek JC; Cree LM
Mol Hum Reprod; 2016 Apr; 22(4):261-71. PubMed ID: 26792869
[TBL] [Abstract][Full Text] [Related]
6. Detection and quantification of mitochondrial DNA deletions from next-generation sequence data.
Bosworth CM; Grandhi S; Gould MP; LaFramboise T
BMC Bioinformatics; 2017 Oct; 18(Suppl 12):407. PubMed ID: 29072135
[TBL] [Abstract][Full Text] [Related]
7. Mitochondrial DNA Sequencing and Heteroplasmy Quantification by Next Generation Sequencing.
Legati A; Ghezzi D; Viscomi C
Methods Mol Biol; 2023; 2615():381-395. PubMed ID: 36807805
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Impact of the sequencing method on the detection and interpretation of mitochondrial DNA length heteroplasmy.
Sturk-Andreaggi K; Parson W; Allen M; Marshall C
Forensic Sci Int Genet; 2020 Jan; 44():102205. PubMed ID: 31783338
[TBL] [Abstract][Full Text] [Related]
10. Mitochondrial DNA enrichment reduced NUMT contamination in porcine NGS analyses.
Wang D; Xiang H; Ning C; Liu H; Liu JF; Zhao X
Brief Bioinform; 2020 Jul; 21(4):1368-1377. PubMed ID: 31204429
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. eKLIPse: a sensitive tool for the detection and quantification of mitochondrial DNA deletions from next-generation sequencing data.
Goudenège D; Bris C; Hoffmann V; Desquiret-Dumas V; Jardel C; Rucheton B; Bannwarth S; Paquis-Flucklinger V; Lebre AS; Colin E; Amati-Bonneau P; Bonneau D; Reynier P; Lenaers G; Procaccio V
Genet Med; 2019 Jun; 21(6):1407-1416. PubMed ID: 30393377
[TBL] [Abstract][Full Text] [Related]
13. Next-Generation Sequencing to Characterize Mitochondrial Genomic DNA Heteroplasmy.
Yang Z; Slone J; Huang T
Curr Protoc; 2022 May; 2(5):e412. PubMed ID: 35532282
[TBL] [Abstract][Full Text] [Related]
14. CmVCall: An automated and adjustable nanopore analysis pipeline for heteroplasmy detection of the control region in human mitochondrial genome.
Jiang L; Liu J; Li S; Wen Y; Zheng X; Qin L; Hou Y; Wang Z
Forensic Sci Int Genet; 2023 Nov; 67():102930. PubMed ID: 37595417
[TBL] [Abstract][Full Text] [Related]
15. A high-throughput next-generation sequencing assay for the mitochondrial genome.
Dames S; Eilbeck K; Mao R
Methods Mol Biol; 2015; 1264():77-88. PubMed ID: 25631005
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Mitochondrial DNA Enrichment for Sensitive Next-Generation Sequencing.
Wu S; Longley MJ; Lujan SA; Kunkel TA; Copeland WC
Methods Mol Biol; 2023; 2615():427-441. PubMed ID: 36807807
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Improving post-natal detection of mitochondrial DNA mutations.
Barcia G; Assouline Z; Magen M; Pennisi A; Rötig A; Munnich A; Bonnefont JP; Steffann J
Expert Rev Mol Diagn; 2020 Oct; 20(10):1003-1008. PubMed ID: 32902337
[TBL] [Abstract][Full Text] [Related]
20. A Novel Next-Generation Sequencing-Based Approach for Concurrent Detection of Mitochondrial DNA Copy Number and Mutation.
Zhou K; Mo Q; Guo S; Liu Y; Yin C; Ji X; Guo X; Xing J
J Mol Diagn; 2020 Dec; 22(12):1408-1418. PubMed ID: 33011442
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
