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Desiree Kianna Elyssia Schenk

age ~35

from Lexington, MA

Desiree Schenk Phones & Addresses

  • Lexington, MA
  • 36 Gilbert Rd, Belmont, MA 02478 • 248-854-3292
  • 437 S 5Th St, Lafayette, IN 47901

Work

  • Company:
    Purdue university - West Lafayette, IN
    Aug 2011
  • Position:
    Nsf graduate research fellow

Education

  • School / High School:
    Purdue University- West Lafayette, IN
    2011
  • Specialities:
    PhD in Biomedical Engineering

Us Patents

  • Target Capture And Barcoding In Monodisperse Droplets

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  • US Patent:
    20210340596, Nov 4, 2021
  • Filed:
    Sep 27, 2019
  • Appl. No.:
    17/281157
  • Inventors:
    - Watertown MA, US
    Kristina Fontanez - Arlington MA, US
    Desiree Schenk - Watertown MA, US
    Yi Xue - Shrewsbury MA, US
  • International Classification:
    C12Q 1/6806
  • Abstract:
    The methods and systems described herein provide capture template particles and an improved emulsion droplet-based target capture and barcoding method thereof. The capture template particles and methods disclosed herein allow capturing targets of interest from biological samples, and barcoding of specific nucleic acids contained in the captured targets. The nucleic acids can be contained within living or nonliving structures, including particles, viruses, and cells. The nucleic acids can include, e.g., DNA or RNA.
  • Hairpin Primer Design For Sequential Pcr Production Of Targeted Sequencing Libraries

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  • US Patent:
    20210054369, Feb 25, 2021
  • Filed:
    Aug 20, 2020
  • Appl. No.:
    16/998685
  • Inventors:
    - Watertown MA, US
    Kristina Fontanez - Arlington MA, US
    Desiree Schenk - Watertown MA, US
  • International Classification:
    C12N 15/10
    C12Q 1/6848
  • Abstract:
    The present disclosure provides a method of hairpin primer design and targeted amplification thereof for creation of targeted sequencing libraries. Generally, the present methods allow for simultaneous construction of targeted sequencing libraries for multiple targeted nucleic acid sequences within a single sample. The presently disclosed methods generate efficient and specific target sequence amplification while avoiding, or significantly reducing, non-specific interaction of multiplex primers, non-specific amplification of sequences due to random priming from molecular “tags” (such as Molecular Identifiers (“MI”) barcodes), and unintentional interactions between gene-specific and universal primers.

Resumes

Desiree Schenk Photo 1

Desiree Schenk Belmont, MA

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Work:
Purdue University
West Lafayette, IN
Aug 2011 to Dec 2014
NSF Graduate Research Fellow
Kettering University
Flint, MI
Apr 2009 to Jul 2011
Undergraduate Researcher
Argonne National Laboratory
Lemont, IL
Jul 2009 to Mar 2011
Fuel Cell Group co-op
General Motors
Warren, MI
Jan 2008 to Mar 2009
Materials Testing co-op
Education:
Purdue University
West Lafayette, IN
2011 to 2014
PhD in Biomedical Engineering
Kettering University
Flint, MI
2007 to 2011
BS in Biochemistry

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