Kylie Montgomery

Research Assistant at UK Dementia Research Institute
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Contact Information
us****@****om
(386) 825-5501
Location
London, England, United Kingdom, UK

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Experience

    • United Kingdom
    • Research
    • 100 - 200 Employee
    • Research Assistant
      • Nov 2021 - Present

      Providing long read sequencing services for research and industry projects. Providing long read sequencing services for research and industry projects.

    • United Kingdom
    • Hospitals and Health Care
    • 700 & Above Employee
    • Clinical Scientist
      • Aug 2019 - Oct 2021

    • United Kingdom
    • Medical Practices
    • 500 - 600 Employee
      • Sep 2017 - Jan 2018

      Report preparation and authorisation for a UKAS accredited genetics laboratory.

      • Jul 2011 - Sep 2017

      Sample receipt, data entry, nucleic acid extraction from various sample types, assay set-up, analysis by various methods, training colleagues, examination audits, assay and equipment verification, SOP writing, competency assessing colleagues, participation in QA schemes, stock control, problem solving and department fire warden.Assays:o Apolipoprotein E genotyping – detection of ε2, ε3, and ε4 alleles.o Bacs-on-Beads KaryoLite and Prenatal testing.o HLA B27 screening o Coeliac screening - HLA alleles linked to an increased predisposition to the disease.o Cytochrome P450 - 2C19 and 2D6 genotyping.o Cystic Fibrosis 139 mutations NGS assay o Duchenne/Becker Muscular Dystrophy - deletions/duplications in DMD gene by MLPA.o Gastro-Intestinal Pathogen Panel - 15 gastro-intestinal pathogens in a multiplex.o Haemochromatosis genotyping - C282Y and H63D mutations in the HFE gene.o HLA tissue typing o Herpes Simplex Virus typing - for distinguishing between HSV Type I and HSV Type II.o Mental retardation panel - copy number changes of regions causing a number of syndromes.o Multiplex STI assay - 7 Sexually Transmitted Infections.o Narcolepsy screening - HLA alleles linked to increased risk of disease.o Paternity testing and human identification o Prader-Willi and Angelman syndrome testing - methylation specific PCR.o Prenatal QF PCR - detects common trisomies and sex chromosome aneuploidies.o Sanjad-Sakati/Kenny Caffey syndromes - 12 base pair deletion in TBCE gene. o Spinal muscular atrophy – copy number changes in Exon 7 of the SMN1 gene by MLPA.o Thrombophilia testing - common mutations in Factor II, Factor V, and MTHFR genes by ARMS PCR. o Uniparental disomy testing o Y chromosome screening - AZF microdeletions associated with male infertility. Show less

      • Oct 2010 - Jul 2011

      Sample receipt, data entry, trouble shooting, inter-departmental communication and team support.

    • United Kingdom
    • Hospitals and Health Care
    • 700 & Above Employee
    • Locum SATO-Specimen Reception
      • Apr 2010 - Oct 2010

      Sample receipt, data entry, dipstick urinalysis and sample preparation for biochemistry. Sample receipt, data entry, dipstick urinalysis and sample preparation for biochemistry.

      • Sep 2009 - Dec 2009

      DNA extraction, assay setup, analysis, stock-take, pipette calibration and environmental monitoring for the department.Assays:o Chlamydia screening - Real-time PCR.o Herpes Simplex Virus typing - for distinguishing between HSV Type I and HSV Type II by real-time PCR.o Haemochromatosis genotyping - C282Y and H63D mutations in the HFE gene by real-time PCR.o Human Papilloma Virus - detection of 37 HPV types by Roche linear array.

      • Jan 2007 - Dec 2009

      Sample receipt, data entry, call centre and troubleshooting.

Education

  • King's College London
    MSc Neuroscience, Distinction
    2019 - 2020
  • Victoria University of Wellington
    Bachelor of Biomedical Science, Human genetics and molecular pathology
    2004 - 2009
  • UCL
    Doctor of Philosophy - PhD, Neuroscience
    2022 -

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