Organizing the world’s variant data for genomic medicine with Mark Kiel | Talking Precision Medicine #12

Organizing the world’s variant data for genomic medicine with Mark Kiel | Talking Precision Medicine #12

Publication date: Jun 14, 2019

In Talking Precision Medicine podcast we sit down with experts on the application of AI and big data analytics in the drug discovery space. Our guests are innovators, business decision makers and thought leaders at the intersection of data and therapeutics. We discuss the promise, practice, challenges, and myths of AI in precision medicine. This show is brought to you by Genialis, and Rafael, our CEO, is your host. Genialis is focused on data integration and predictive modeling of disease biology to help accelerate the discovery and de-risk the development of novel therapeutics. Today we speak with Mark Kiel. Mark is the founder and Chief Scientific Officer at Genomenon where he shepherds the product vision and implementation of the Mastermind suite of software tools. He completed an MD / PhD fellowship in Molecular Genetic Pathology at the University of Michigan. In this episode, Mark describes the genesis of his vision to organize the world’s molecular data and his journey to realize the promise of genomic medicine.

Concepts Keywords
African American Mastermind product
AH Analytics tools
Air Cancer care
AMG Software tools
Anxiety Analytic tools
Artificial Intelligence Healthcare
Asia Software world
Asian Open source tools
Beatles Patrick disorders
Bill Cancer
Biomarker Tumors
Black Box Variant disease
Brisk Different cancers
Buzzword Nerve degenerative diseases
Cancer Forms disease
CEO Diabetes
Chaperone Apologetic diseases
China Lymphomas
Clinical Trial Psychiatric disorders
Clone Broad strokes
Cohort Psychiatric disease
Colonoscopy Leukemias
Computational Intelligence PTSD
Concrete Depression
Conservative Very common diseases
Constellation Frank cancer
Curator The Organ
Deep Learning Songs
Degenerative Diseases Albums
Depression Creative works
Diabetes 9
Diagnostician Genomics
District Bioinformatics
Division Drug discovery
DNA Artificial intelligence
Dovetail Machine learning
Elephant Flash
Empirical Evidence Drug development
Ethnic Group Human genome
Evolutionary Biologist
Excel
Exeter
Faithfully
Forest
Frequency
Gene
Genetic
Genetic Pathway
Genetic Variance
Genetics
Genie
Genome
Genomic Medicine
Genomic Sequencing
Genomics
Gold
Goldmine
Graduate School
Headway
Healthcare
Hedge
Informs
Instamatic
ISS
Iwas
Jin
Kiel
Leukemias
Lymphomas
Maciste
Main Event
Malignancy
Mammography
Marky Mark
Mastermind
Mat
Medicine
Michigan
Mints
Mirror
Molecular Genetic
Mutation
Nerve
Newborn Screening
Oncology
Ossified
Paradigm
Pathogenesis
Pathogenic
Pathologist
Pathology
Pharma
PhD
Pinnacle
Podcast
Polymorphism
Precision Medicine
Predictive Modeling
Prognosis
Psychiatric Disorders
PTSD
Rare Disease
Reactionary
Remission
Sanitation
Scandinavia
Segregation
Sequencing
Spectrum
Stakeholder
Thes
Tipping Point
Triage
Tsunami
Variance
Writ

Semantics

Type Source Name
gene UNIPROT MARK1
gene UNIPROT SIT1
disease MESH development
drug DRUGBANK Nonoxynol-9
gene UNIPROT PDC
gene UNIPROT FOXD3

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