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Keegan Kelsey

About

Keegan Kelsey

Building and learning · San Francisco, CA

Keegan Kelsey, Ph.D., is a scientist, an engineer, and a creative. Most recently a Director of Engineering at DNAnexus, Dr. Kelsey collaborates extensively across an organization (Product, Engineering, Scientific, Business Units, Marketing, and Executive teams), supporting the progress and development of data products. With a specialization in clinical and multi-omic data, he has over 10 years of experience in the technology/biotechnology sectors and over 18 years of experience in scientific research.

Dr. Kelsey received his doctorate from Cornell University in Ithaca, New York, in 2016. He was an Insight Data Science Fellow in 2015 and was subsequently a Data Scientist at 23andMe. He received his bachelor’s degree from The School of the Art Institute of Chicago.

Past research and engineering efforts have involved a diverse array of topics in both human and model organisms, with direct bioinformatics, software engineering, and analysis experience in genetics, population genetics (germline and somatic), clinical/phenotypic data, -omic data (genomic, transcriptomic, epigenomic, proteomic), and metadata such as annotations and ontologies. Currently, efforts are spent exploring, optimizing, integrating, inferring and analyzing disparate data with an emphasis on data-centric discovery and product delivery.

Education

  1. Cornell University

    2009 – 2015

    Ph.D., Genetics, Genomics & Development

    Ithaca, NY

    Department of Molecular Biology & Genetics

    Minor in Biometry

  2. The School of the Art Institute of Chicago

    2005

    B.A., Visual and Critical Studies

    Chicago, IL

Experience

  1. DNAnexus

    2019 – 2026

    Director, Engineering (2022)

    Mountain View, CA

    Previously Principal Scientist (2020) · Senior Scientist (2019)

    DNAnexus provides a cloud-based platform to help integrate molecular and clinical data for downstream, scalable compute and production-grade monitoring and delivery of data. I worked with a team of scientists and engineers to deliver a variety of products on the platform.

  2. 23andMe

    2015 – 2018

    Senior Data Scientist (2018)

    Mountain View, CA

    Previously Data Scientist

    If you believe in the power of large-scale genetic research, which I do, then 23andMe should already be on your radar! 23andMe is a direct-to-consumer company that helps customers access and understand their own genetic information. I helped with various projects at the company.

  3. Insight Data Science

    2015

    Data Science Fellow

    Palo Alto, CA

    Insight Data Science is an intensive 7-week postdoctoral training fellowship bridging the gap between academia and industry. Just prior to earning a Ph.D., I was a Fellow in the SV 2015A session at Insight. Here, I created a novel data project and used that project to interview with data-centric companies.

  4. Cornell University

    2009 – 2015

    Graduate Research Assistant

    Ithaca, NY

    I was fortunate to be advised by Dr. Andrew G. Clark, a population geneticist and member of the National Academy of Sciences. My Ph.D. work involved understanding the natural genetic architecture underlying Position Effect Variegation (PEV), a proxy for epigenetic context in a genome. To this end, I generated experimental data and performed end-to-end analysis of whole-genome sequence data and RNA-seq from over 100 individuals. During this time, I was also a Teaching Assistant for Andy's course, Human Genetics, and for Chip Aquadro's course, Personalized Genomics and Medicine.

  5. University of Iowa Hospitals and Clinics

    2005 – 2009

    Research Assistant

    Iowa City, IA

    Prior to starting my Ph.D., I spent four years in the lab of Dr. Jeffrey C. Murray studying associations between genetic factors and preterm birth, a common, complex disease that impacts roughly 1 in every 8 babies born in the United States. Mentorship from Jeff (University of Iowa, past president of ASHG, Gates Foundation), a sense of discovery, potential impact, and a love for problem solving were all strong reasons I developed a passion for research and the sciences. Here, I performed genetic and statistical analysis of preterm birth (work that resulted in four publications), assisted in sample collection, sample processing, and database management for a University-wide biorepository, and performed general lab procedures including PCR, TaqMan assays, Sanger sequencing, and gel electrophoresis.

Publications

  1. Interactions between PDA-associated polymorphisms and genetic ancestry alter ductus arteriosus gene expression

    2022

    Clyman RI, Hills NK, Dagle JM, Murray JC, Kelsey K

    Pediatric Research 91(4): 903–911

  2. Functional consequences of variation in Y chromosome heterochromatin in Drosophila

    2018

    Kelsey KJP, Clark AG

    In preparation

  3. Variation in Position Effect Variegation within a natural population

    2017

    Kelsey KJP, Clark AG

    Genetics 207(3): 1157–1166

  4. Candidate genetic modifiers of retinitis pigmentosa identified by exploiting natural variation in Drosophila

    2016

    Chow CY, Kelsey KJ, Wolfner MF, Clark AG

    Human Molecular Genetics 25(4): 651–659

  5. Polymorphisms in the fetal progesterone receptor and a calcium-activated potassium channel isoform are associated with preterm birth in an Argentinian population

    2013

    Mann PC, Cooper ME, Ryckman KK, Comas B, Gili J, Crumley S, Bream EN, Byers HM, Piester T, Schaefer A, Christine PJ, Lawrence A, Schaa KL, Kelsey KJ, Berends SK, Momany AM, Gadow E, Cosentino V, Castilla EE, López Camelo J, Saleme C, Day LJ, England SK, Marazita ML, Dagle JM, Murray JC

    Journal of Perinatology 33(5): 336–340

  6. Genetic associations of surfactant protein D and angiotensin-converting enzyme with lung disease in preterm neonates

    2012

    Ryckman KK, Dagle JM, Kelsey K, Momany AM, Murray JC

    Journal of Perinatology 32(5): 349–355

  7. Replication of genetic associations in the inflammation, complement, and coagulation pathways with intraventricular hemorrhage in LBW preterm neonates

    2011

    Ryckman KK, Dagle JM, Kelsey K, Momany AM, Murray JC

    Pediatric Research 70(1): 90–95

  8. Determination of genetic predisposition to patent ductus arteriosus in preterm infants

    2009

    Dagle JM, Lepp NT, Cooper ME, Schaa KL, Kelsey KJ, Orr KL, Caprau D, Zimmerman CR, Steffen KM, Johnson KJ, Marazita ML, Murray JC

    Pediatrics 123(4): 1116–1123