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 *

175 related articles for article (PubMed ID: 39350015)

  • 1. Fine mapping of RNA isoform diversity using an innovative targeted long-read RNA sequencing protocol with novel dedicated bioinformatics pipeline.
    Aucouturier C; Soirat N; Castéra L; Bertrand D; Atkinson A; Lavolé T; Goardon N; Quesnelle C; Levilly J; Barbachou S; Legros A; Caron O; Crivelli L; Denizeau P; Berthet P; Ricou A; Boulouard F; Vaur D; Krieger S; Leman R
    BMC Genomics; 2024 Sep; 25(1):909. PubMed ID: 39350015
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Transcript Profiling Using Long-Read Sequencing Technologies.
    Bayega A; Wang YC; Oikonomopoulos S; Djambazian H; Fahiminiya S; Ragoussis J
    Methods Mol Biol; 2018; 1783():121-147. PubMed ID: 29767360
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Targeted RNA-seq successfully identifies normal and pathogenic splicing events in breast/ovarian cancer susceptibility and Lynch syndrome genes.
    Brandão RD; Mensaert K; López-Perolio I; Tserpelis D; Xenakis M; Lattimore V; Walker LC; Kvist A; Vega A; Gutiérrez-Enríquez S; Díez O; ; de la Hoya M; Spurdle AB; De Meyer T; Blok MJ
    Int J Cancer; 2019 Jul; 145(2):401-414. PubMed ID: 30623411
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Full-length isoform concatenation sequencing to resolve cancer transcriptome complexity.
    Wijeratne S; Gonzalez MEH; Roach K; Miller KE; Schieffer KM; Fitch JR; Leonard J; White P; Kelly BJ; Cottrell CE; Mardis ER; Wilson RK; Miller AR
    BMC Genomics; 2024 Jan; 25(1):122. PubMed ID: 38287261
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Characterization of three alternative transcripts of the BRCA1 gene in patients with breast cancer and a family history of breast and/or ovarian cancer who tested negative for pathogenic mutations.
    Gambino G; Tancredi M; Falaschi E; Aretini P; Caligo MA
    Int J Mol Med; 2015 Apr; 35(4):950-6. PubMed ID: 25683334
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A survey of the complex transcriptome from the highly polyploid sugarcane genome using full-length isoform sequencing and de novo assembly from short read sequencing.
    Hoang NV; Furtado A; Mason PJ; Marquardt A; Kasirajan L; Thirugnanasambandam PP; Botha FC; Henry RJ
    BMC Genomics; 2017 May; 18(1):395. PubMed ID: 28532419
    [TBL] [Abstract][Full Text] [Related]  

  • 7. BRCA1 and BRCA2 whole cDNA analysis in unsolved hereditary breast/ovarian cancer patients.
    Montalban G; Bonache S; Bach V; Gisbert-Beamud A; Tenés A; Moles-Fernández A; López-Fernández A; Carrasco E; Balmaña J; Diez O; Gutiérrez-Enríquez S
    Cancer Genet; 2021 Nov; 258-259():10-17. PubMed ID: 34237702
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Tracking Alternatively Spliced Isoforms from Long Reads by SpliceHunter.
    Kuang Z; Canzar S
    Methods Mol Biol; 2018; 1751():73-88. PubMed ID: 29508290
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Implementation of next-generation sequencing for molecular diagnosis of hereditary breast and ovarian cancer highlights its genetic heterogeneity.
    Pinto P; Paulo P; Santos C; Rocha P; Pinto C; Veiga I; Pinheiro M; Peixoto A; Teixeira MR
    Breast Cancer Res Treat; 2016 Sep; 159(2):245-56. PubMed ID: 27553368
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Merging short and stranded long reads improves transcript assembly.
    Kainth AS; Haddad GA; Hall JM; Ruthenburg AJ
    PLoS Comput Biol; 2023 Oct; 19(10):e1011576. PubMed ID: 37883581
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Illuminating the dark side of the human transcriptome with long read transcript sequencing.
    Kuo RI; Cheng Y; Zhang R; Brown JWS; Smith J; Archibald AL; Burt DW
    BMC Genomics; 2020 Oct; 21(1):751. PubMed ID: 33126848
    [TBL] [Abstract][Full Text] [Related]  

  • 13. PacBio single molecule long-read sequencing provides insight into the complexity and diversity of the Pinctada fucata martensii transcriptome.
    Zhang H; Xu H; Liu H; Pan X; Xu M; Zhang G; He M
    BMC Genomics; 2020 Jul; 21(1):481. PubMed ID: 32660426
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Screening of
    Montalban G; Bonache S; Moles-Fernández A; Gisbert-Beamud A; Tenés A; Bach V; Carrasco E; López-Fernández A; Stjepanovic N; Balmaña J; Diez O; Gutiérrez-Enríquez S
    J Med Genet; 2019 Feb; 56(2):63-74. PubMed ID: 30472649
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Detecting splicing patterns in genes involved in hereditary breast and ovarian cancer.
    Davy G; Rousselin A; Goardon N; Castéra L; Harter V; Legros A; Muller E; Fouillet R; Brault B; Smirnova AS; Lemoine F; de la Grange P; Guillaud-Bataille M; Caux-Moncoutier V; Houdayer C; Bonnet F; Blanc-Fournier C; Gaildrat P; Frebourg T; Martins A; Vaur D; Krieger S
    Eur J Hum Genet; 2017 Oct; 25(10):1147-1154. PubMed ID: 28905878
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Methodologies for Transcript Profiling Using Long-Read Technologies.
    Oikonomopoulos S; Bayega A; Fahiminiya S; Djambazian H; Berube P; Ragoussis J
    Front Genet; 2020; 11():606. PubMed ID: 32733532
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Single-cell long-read targeted sequencing reveals transcriptional variation in ovarian cancer.
    Byrne A; Le D; Sereti K; Menon H; Vaidya S; Patel N; Lund J; Xavier-Magalhães A; Shi M; Liang Y; Sterne-Weiler T; Modrusan Z; Stephenson W
    Nat Commun; 2024 Aug; 15(1):6916. PubMed ID: 39134520
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Dynamic nanopore long-read sequencing analysis of HIV-1 splicing events during the early steps of infection.
    Nguyen Quang N; Goudey S; Ségéral E; Mohammad A; Lemoine S; Blugeon C; Versapuech M; Paillart JC; Berlioz-Torrent C; Emiliani S; Gallois-Montbrun S
    Retrovirology; 2020 Aug; 17(1):25. PubMed ID: 32807178
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A transcriptome atlas of rabbit revealed by PacBio single-molecule long-read sequencing.
    Chen SY; Deng F; Jia X; Li C; Lai SJ
    Sci Rep; 2017 Aug; 7(1):7648. PubMed ID: 28794490
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Identification of Protein Isoforms Using Reference Databases Built from Long and Short Read RNA-Sequencing.
    Tay AP; Hamey JJ; Martyn GE; Wilson LOW; Wilkins MR
    J Proteome Res; 2022 Jul; 21(7):1628-1639. PubMed ID: 35612954
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.