BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

203 related articles for article (PubMed ID: 34389649)

  • 1. Deciphering Neurodegenerative Diseases Using Long-Read Sequencing.
    Su Y; Fan L; Shi C; Wang T; Zheng H; Luo H; Zhang S; Hu Z; Fan Y; Dong Y; Yang J; Mao C; Xu Y
    Neurology; 2021 Aug; 97(9):423-433. PubMed ID: 34389649
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Long-Read DNA Sequencing: Recent Advances and Remaining Challenges.
    Warburton PE; Sebra RP
    Annu Rev Genomics Hum Genet; 2023 Aug; 24():109-132. PubMed ID: 37075062
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Evaluation of strategies for the assembly of diverse bacterial genomes using MinION long-read sequencing.
    Goldstein S; Beka L; Graf J; Klassen JL
    BMC Genomics; 2019 Jan; 20(1):23. PubMed ID: 30626323
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Single-Molecule Sequencing: Towards Clinical Applications.
    Ameur A; Kloosterman WP; Hestand MS
    Trends Biotechnol; 2019 Jan; 37(1):72-85. PubMed ID: 30115375
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Long-read sequencing for rare human genetic diseases.
    Mitsuhashi S; Matsumoto N
    J Hum Genet; 2020 Jan; 65(1):11-19. PubMed ID: 31558760
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Long-read sequencing improves diagnostic rate in neuromuscular disorders.
    Owusu R; Savarese M
    Acta Myol; 2023; 42(4):123-128. PubMed ID: 38406378
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification and characterization of repeat expansions in neurological disorders: Methodologies, tools, and strategies.
    Leitão E; Schröder C; Depienne C
    Rev Neurol (Paris); 2024 May; 180(5):383-392. PubMed ID: 38594146
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Longshot enables accurate variant calling in diploid genomes from single-molecule long read sequencing.
    Edge P; Bansal V
    Nat Commun; 2019 Oct; 10(1):4660. PubMed ID: 31604920
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Nanopore sequencing: Review of potential applications in functional genomics.
    Kono N; Arakawa K
    Dev Growth Differ; 2019 Jun; 61(5):316-326. PubMed ID: 31037722
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Application of long-read sequencing to the detection of structural variants in human cancer genomes.
    Sakamoto Y; Zaha S; Suzuki Y; Seki M; Suzuki A
    Comput Struct Biotechnol J; 2021; 19():4207-4216. PubMed ID: 34527193
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genome assembly using Nanopore-guided long and error-free DNA reads.
    Madoui MA; Engelen S; Cruaud C; Belser C; Bertrand L; Alberti A; Lemainque A; Wincker P; Aury JM
    BMC Genomics; 2015 Apr; 16(1):327. PubMed ID: 25927464
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Complete sequencing of expanded SAMD12 repeats by long-read sequencing and Cas9-mediated enrichment.
    Mizuguchi T; Toyota T; Miyatake S; Mitsuhashi S; Doi H; Kudo Y; Kishida H; Hayashi N; Tsuburaya RS; Kinoshita M; Fukuyama T; Fukuda H; Koshimizu E; Tsuchida N; Uchiyama Y; Fujita A; Takata A; Miyake N; Kato M; Tanaka F; Adachi H; Matsumoto N
    Brain; 2021 May; 144(4):1103-1117. PubMed ID: 33791773
    [TBL] [Abstract][Full Text] [Related]  

  • 14. PacBio Sequencing and Its Applications.
    Rhoads A; Au KF
    Genomics Proteomics Bioinformatics; 2015 Oct; 13(5):278-89. PubMed ID: 26542840
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Improving nanopore read accuracy with the R2C2 method enables the sequencing of highly multiplexed full-length single-cell cDNA.
    Volden R; Palmer T; Byrne A; Cole C; Schmitz RJ; Green RE; Vollmers C
    Proc Natl Acad Sci U S A; 2018 Sep; 115(39):9726-9731. PubMed ID: 30201725
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Applications and potentials of nanopore sequencing in the (epi)genome and (epi)transcriptome era.
    Xie S; Leung AW; Zheng Z; Zhang D; Xiao C; Luo R; Luo M; Zhang S
    Innovation (Camb); 2021 Nov; 2(4):100153. PubMed ID: 34901902
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Scaffolding of a bacterial genome using MinION nanopore sequencing.
    Karlsson E; Lärkeryd A; Sjödin A; Forsman M; Stenberg P
    Sci Rep; 2015 Jul; 5():11996. PubMed ID: 26149338
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Modification mapping by nanopore sequencing.
    White LK; Hesselberth JR
    Front Genet; 2022; 13():1037134. PubMed ID: 36386798
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Interrogating the "unsequenceable" genomic trinucleotide repeat disorders by long-read sequencing.
    Liu Q; Zhang P; Wang D; Gu W; Wang K
    Genome Med; 2017 Jul; 9(1):65. PubMed ID: 28720120
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Testing assembly strategies of Francisella tularensis genomes to infer an evolutionary conservation analysis of genomic structures.
    Neubert K; Zuchantke E; Leidenfrost RM; Wünschiers R; Grützke J; Malorny B; Brendebach H; Al Dahouk S; Homeier T; Hotzel H; Reinert K; Tomaso H; Busch A
    BMC Genomics; 2021 Nov; 22(1):822. PubMed ID: 34773979
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.