Paul Hengen

Paul Hengen

Bioinformaticist at NanoString Technologies

Greater Seattle Area

Current
Past
  • Assistant Research Scientist at City of Hope National Medical Center
  • Staff Scientist at USC Keck School of Medicine
  • R&D Scientist at Applied Biosystems
  • Post-Doctoral Fellow and Staff Scientist at National Cancer Institute
  • Technical Columnist at Trends in Biochemical Sciences
Education
  • Carleton University
  • University of Vermont
  • University of Maryland College Park
Connections
261 connections
Industry
Biotechnology
Websites

Paul Hengen’s Summary

I have equal experience in molecular genetics and computational biology. My goal has been to combine computer science and genetics for making discoveries of medical importance. I am particularly interested in the molecular pathology of disease, personalized medicine, and medical or pharmaceutical discovery.

Keywords: Molecular Genetics, Computational Biology, Bioinformatics, Microbiology, Cancer Research.

Paul Hengen’s Specialties:

Gene Target and Biomarker Discovery.

Genetics Domain Object Model Expert, Database Design.

Genetic Data Extraction, Conversion and Analysis (10+ years of Perl programming experience), Combining genotype and gene expression data.

DNA binding-site prediction for annotation (Transcription Factors, Human Splice Junctions), DNA and RNA sequence analysis using DNA sequence Logos (NAR 18:6097-6100) and Walkers (NAR 25:4408-4415).


Paul Hengen’s Experience

  • Bioinformaticist

    NanoString Technologies

    (Privately Held; Biotechnology industry)

    August 2009Present (4 months)

    NanoString Technologies manufactures and sells the nCounter Analysis System, a research platform that utilizes a novel digital technology that is based on direct multiplexed measurement of gene expression and offers high levels of precision and sensitivity (<1 copy per cell).  The technology uses molecular barcodes and single molecule imaging to detect and count hundreds of unique nucleic acids in a single reaction. Although originally designed for gene expression profiling, the nCounter system can be utilized for direct measurment of individual molecules in a single reaction without amplification for many biological applications. NanoString's technology may be used for basic research, translational medicine, and molecular diagnostics.

  • Assistant Research Scientist

    City of Hope National Medical Center

    (Biotechnology industry)

    August 2007February 2009 (1 year 7 months)

    Identified molecular markers of risk for therapy-related
    myelodysplastic syndrome (t-MDS) after autologous bone
    marrow transplantation with hematopoietic stem cells (HSC).
    t-MDS and acute myologenous leukemia (AML) are serious bone
    marrow complications following cancer therapy. We used
    Affymetrix Gene Chip hybridization arrays to identify genes
    misregulated within peripheral blood stem cells (PBSC) and
    bone marrow stem cells in patients undergoing bone marrow
    transplant (BMT). Gene Set Enrichment Analysis (GSEA)
    revealed many genes within cell signaling pathways altered
    in their expression levels and these genes were further
    analyzed for their potential as therapeutic targets.
    Follow-up studies with mathematical models of nuclear
    transcription factor binding sites should elucidate the
    mechanisms of gene regulation in the development of leukemia
    and secondary bone marrow cancers.

  • Staff Scientist

    USC Keck School of Medicine

    (Biotechnology industry)

    August 2006April 2007 (9 months)

    As part of a team, worked in collaboration with wet bench
    scientists to identify molecular markers of prostate cancer
    progression and metastasis to bone. The androgen receptor
    (AR) belongs to a family of ligand-activated nuclear
    receptors that mediate gene expression through
    transcriptional activation. The role of the AR in prostate
    cancer initiation and progression is well established;
    however, there is little knowledge of how AR target genes
    play a role in prostate cancer initiation and progression,
    typically resulting in secondary metastasis to the bone
    marrow. We combined the laboratory method of ChIP-on-chip
    and a bioinformatic approach utilizing a mathematical model
    of AR DNA binding sites to discover and characterize novel
    AR target genes in prostate cancer cells. The goal was to
    investigate the possible role of these genes in formation of
    bone marrow cancer.

  • R&D Scientist

    Applied Biosystems

    (Biotechnology industry)

    April 2000August 2005 (5 years 5 months)

    For this company, personally designed the genetics object
    model for ABI's instrumentation and data analysis software.
    This object-oriented domain model, based on fundamental
    principles of Mendelian characterization, was designed to be
    independent of instrumentation. The design allows for
    genetic data to be gathered from phenotype, genotype, and
    gene expression information sources and then combined for
    the purpose of association studies, mathematical modeling,
    and data-mining. The genetics object model was specifically
    designed to aid the discovery of new predictors of genetic
    processes (biomarkers) and for applications in molecular
    medicine.

  • Post-Doctoral Fellow and Staff Scientist

    National Cancer Institute

    (Biotechnology industry)

    19921998 (6 years )

    As part of a team used information theory techniques
    to create mathematical models of DNA binding sites. By
    comparing the models to natural binding sites, made
    predictions about the properties of DNA-protein
    interactions concerning transcriptional regulation (gene
    expression) and other molecular recognition. Showed the
    feasibility of using such a method for scanning DNA
    sequences to predict sites bound by the Factor for Inversion
    Stimulation (Fis), a pleiotropic protein that enhances site-
    specific recombination, controls DNA replication, and
    regulates transcription of a number of genes in Escherichia
    coli and Salmonella typhimurium.

  • Technical Columnist

    Trends in Biochemical Sciences

    (Biotechnology industry)

    19931997 (4 years )

    Authored over 45 articles published as a `Methods and Reagents' monthly series within Trends in Biochemical Sciences from 1993 through 1997. All manuscripts are freely available on the web from my archive site at: http://www-lecb.ncifcrf.gov/~pnh/readme.html


Paul Hengen’s Education

  • Carleton University

    Ph.D. , Molecular Genetics , 19851991

    Activities and Societies:
    Tunnel Rat, Canadian Inland Telemark Surf Team, Midnight Canal Skater's Club, Prince of Wales Polar Bear Jacuzzi Runners
  • University of Vermont

    M.S. , Microbiology , 19831985

  • University of Maryland College Park

    B.S. , Microbiology , 19791983

    Activities and Societies:
    Phi Sigma National Honorary Fraternity, Kappa Kappa Psi National Honorary Fraternity, Maryland Marching Band

Additional Information

Paul Hengen’s Websites:

Paul Hengen’s Interests:

I am interested in the molecular pathology of disease, personalized medicine, and medical or pharmaceutical discovery.

Paul Hengen’s Groups:

  •    Carleton University Alumni
  •    Lifesciences Opportunities in US
  •    Chessmasters
  •    University of Vermont Alumni
  •    Computational Biology
  •    Bioinformatics geeks
  •    MolecularLab (Community of Molecular Biology & Biotech companies, students, researchers)
  •    University of Maryland, College Park Alumni Association
  •    Lindy Hop
  •    Personalized Medicine
  •    American Society of Human Genetics (ASHG)
  •    Biomarkers in Discovery & Development
  •    Cancer Sequencing
  •    NGS (Next Generation Sequencing)
  •    Genomics: Next Generation DNA Sequencing (NGS) and Microarray

Paul Hengen’s Contact Settings

Interested In:

  • career opportunities
  • consulting offers
  • new ventures
  • expertise requests
  • reference requests
  • getting back in touch

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