Search Results - "Reeser, Julie W"

Refine Results
  1. 1

    Fibroblast growth factor receptors in cancer: genetic alterations, diagnostics, therapeutic targets and mechanisms of resistance by Krook, Melanie A., Reeser, Julie W., Ernst, Gabrielle, Barker, Hannah, Wilberding, Max, Li, Gary, Chen, Hui-Zi, Roychowdhury, Sameek

    Published in British journal of cancer (02-03-2021)
    “…Fibroblast growth factor receptors (FGFRs) are aberrantly activated through single-nucleotide variants, gene fusions and copy number amplifications in 5–10% of…”
    Get full text
    Journal Article
  2. 2

    Evaluation of Hybridization Capture Versus Amplicon-Based Methods for Whole-Exome Sequencing by Samorodnitsky, Eric, Jewell, Benjamin M., Hagopian, Raffi, Miya, Jharna, Wing, Michele R., Lyon, Ezra, Damodaran, Senthilkumar, Bhatt, Darshna, Reeser, Julie W., Datta, Jharna, Roychowdhury, Sameek

    Published in Human mutation (01-09-2015)
    “…ABSTRACT Next‐generation sequencing has aided characterization of genomic variation. While whole‐genome sequencing may capture all possible mutations,…”
    Get full text
    Journal Article
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7
  8. 8
  9. 9
  10. 10
  11. 11

    Performance evaluation for rapid detection of pan-cancer microsatellite instability with MANTIS by Kautto, Esko A, Bonneville, Russell, Miya, Jharna, Yu, Lianbo, Krook, Melanie A, Reeser, Julie W, Roychowdhury, Sameek

    Published in Oncotarget (31-01-2017)
    “…In current clinical practice, microsatellite instability (MSI) and mismatch repair deficiency detection is performed with MSI-PCR and immunohistochemistry…”
    Get full text
    Journal Article
  12. 12
  13. 13

    Cancer Driver Log (CanDL): Catalog of Potentially Actionable Cancer Mutations by Damodaran, Senthilkumar, Miya, Jharna, Kautto, Esko, Zhu, Eliot, Samorodnitsky, Eric, Datta, Jharna, Reeser, Julie W, Roychowdhury, Sameek

    Published in The Journal of molecular diagnostics : JMD (01-09-2015)
    “…Massively parallel sequencing technologies have enabled characterization of genomic alterations across multiple tumor types. Efforts have focused on…”
    Get full text
    Journal Article
  14. 14

    Comparison of Custom Capture for Targeted Next-Generation DNA Sequencing by Samorodnitsky, Eric, Datta, Jharna, Jewell, Benjamin M, Hagopian, Raffi, Miya, Jharna, Wing, Michele R, Damodaran, Senthilkumar, Lippus, Juliana M, Reeser, Julie W, Bhatt, Darshna, Timmers, Cynthia D, Roychowdhury, Sameek

    “…Targeted, capture-based DNA sequencing is a cost-effective method to focus sequencing on a coding region or other customized region of the genome. There are…”
    Get full text
    Journal Article
  15. 15
  16. 16
  17. 17

    Targeted RNA Sequencing Assay to Characterize Gene Expression and Genomic Alterations by Martin, Dorrelyn P, Miya, Jharna, Reeser, Julie W, Roychowdhury, Sameek

    Published in Journal of visualized experiments (04-08-2016)
    “…RNA sequencing (RNAseq) is a versatile method that can be utilized to detect and characterize gene expression, mutations, gene fusions, and noncoding RNAs…”
    Get full text
    Journal Article
  18. 18
  19. 19
  20. 20

    Cancer Driver Log (CanDL) by Damodaran, Senthilkumar, Miya, Jharna, Kautto, Esko, Zhu, Eliot, Samorodnitsky, Eric, Datta, Jharna, Reeser, Julie W, Roychowdhury, Sameek

    Published in The Journal of molecular diagnostics : JMD (01-09-2015)
    “…Massively parallel sequencing technologies have enabled characterization of genomic alterations across multiple tumor types. Efforts have focused on…”
    Get full text
    Journal Article