Personal Information
Entreprise/Lieu de travail
Greater Boston Area United States
Profession
Co-Founder and Chief Executive Officer at WuXi NextCODE
Secteur d’activité
Medical / Health Care / Pharmaceuticals
Site Web
www.hannessmarason.com
À propos
Hannes Thor Smárason is Co-Founder and Chief Executive Officer of WuXi NextCODE, a genomic information company using sequence data to improve health for people around the world.
Mots-clés
genome sequencing
rare diseases
genomic data
genome analysis
personalized medicine
genome interpretation
genomics
nextcode health
decode genetics
wuxi nextcode
genomics england
cancer
nextcode exchange
genome database
genome data storage
nextcode
genomically ordered relational database (gor)
sidra medical and research center
genomic analysis
genetic variants
big data
23andme
national cancer institute
data storage
genomic medicine
wuxi
genomic data sharing
clinical sequencing
population-scale sequencing
next-generation sequencing
genomic data analysis
boston children's hospital
baylor college of medicine
genomics-based medicine
000 genomes project
genomics-driven medicine
genetic variation
whole genome sequencing
genome storage
human genome
cancer tumor analysis
gene sequencing
cloud-based analysis
data sharing
population genomics
ashg 2016
parent project muscular dystrophy
patient-centric communities
rareconnect
simons foundation autism research initiative
patientslikeme
mygene2
d wuxi nextcode
genetic alliance
charlotte & gwyneth gray foundation
national patient-centered clinical research networ
spark
data silos
dtc genetic testing
genetic variant
carrier status
fda
nci-match
genetic testing
alk testing
tapur
efgr testing
brca testing
her2 testing
asco
clinical oncology
precision medicine
national institutes of health
qatar genome project
fudan children’s hospital
10
claritas genomics
mayo clinic
diagnostic odyssey
genomics-based care
the partnership aims to accelerate and augment the
pediatric genetic disorders
claritas genomics and nextcode have established a
global genes
integrated approach to genomics-based care for rar
autism
simons simplex collection
autism spectrum disorder
american society of human genetics (ashg)
genomic-based medicine
whole-genome databases
haplotype reference consortium (hrc)
queensland institute of medical research
university college dublin
saitama medical university
100k genomes project
rare genetic diseases
100000 genomes project
human longevity
regeneron
bloomberg
illumina
genome databases
genetic diseases
tumor profiling
charcot-marie-tooth syndrome
plos blog
clinical genomics
biocentury
acord
bio-it world
xconomy
nature biotechnology
stanford school of medicine
anzac research institute
genoimc data
large-scale sequencing
global medicine
100
gene variants
whole-genome sequencing
genetic mutations and disease
genomic research centers
genetics of disease
genomic sequencing and analysis
low-cost genome sequencing
whole exome sequencing
raw sequence data
genetic datasets
hannes smarason
Tout plus
Présentations
(11)J’aime
(2)Maintaining Momentum Post-ASHG 2014: Maximizing the Value of Large Genomic Databases
Hannes Smárason
•
il y a 9 ans
Population-Scale Research Efforts Enabled by Progress in Sequencing
Hannes Smárason
•
il y a 9 ans
Personal Information
Entreprise/Lieu de travail
Greater Boston Area United States
Profession
Co-Founder and Chief Executive Officer at WuXi NextCODE
Secteur d’activité
Medical / Health Care / Pharmaceuticals
Site Web
www.hannessmarason.com
À propos
Hannes Thor Smárason is Co-Founder and Chief Executive Officer of WuXi NextCODE, a genomic information company using sequence data to improve health for people around the world.
Mots-clés
genome sequencing
rare diseases
genomic data
genome analysis
personalized medicine
genome interpretation
genomics
nextcode health
decode genetics
wuxi nextcode
genomics england
cancer
nextcode exchange
genome database
genome data storage
nextcode
genomically ordered relational database (gor)
sidra medical and research center
genomic analysis
genetic variants
big data
23andme
national cancer institute
data storage
genomic medicine
wuxi
genomic data sharing
clinical sequencing
population-scale sequencing
next-generation sequencing
genomic data analysis
boston children's hospital
baylor college of medicine
genomics-based medicine
000 genomes project
genomics-driven medicine
genetic variation
whole genome sequencing
genome storage
human genome
cancer tumor analysis
gene sequencing
cloud-based analysis
data sharing
population genomics
ashg 2016
parent project muscular dystrophy
patient-centric communities
rareconnect
simons foundation autism research initiative
patientslikeme
mygene2
d wuxi nextcode
genetic alliance
charlotte & gwyneth gray foundation
national patient-centered clinical research networ
spark
data silos
dtc genetic testing
genetic variant
carrier status
fda
nci-match
genetic testing
alk testing
tapur
efgr testing
brca testing
her2 testing
asco
clinical oncology
precision medicine
national institutes of health
qatar genome project
fudan children’s hospital
10
claritas genomics
mayo clinic
diagnostic odyssey
genomics-based care
the partnership aims to accelerate and augment the
pediatric genetic disorders
claritas genomics and nextcode have established a
global genes
integrated approach to genomics-based care for rar
autism
simons simplex collection
autism spectrum disorder
american society of human genetics (ashg)
genomic-based medicine
whole-genome databases
haplotype reference consortium (hrc)
queensland institute of medical research
university college dublin
saitama medical university
100k genomes project
rare genetic diseases
100000 genomes project
human longevity
regeneron
bloomberg
illumina
genome databases
genetic diseases
tumor profiling
charcot-marie-tooth syndrome
plos blog
clinical genomics
biocentury
acord
bio-it world
xconomy
nature biotechnology
stanford school of medicine
anzac research institute
genoimc data
large-scale sequencing
global medicine
100
gene variants
whole-genome sequencing
genetic mutations and disease
genomic research centers
genetics of disease
genomic sequencing and analysis
low-cost genome sequencing
whole exome sequencing
raw sequence data
genetic datasets
hannes smarason
Tout plus