[HTML][HTML] The UK10K project identifies rare variants in health and disease
Statistics group Ciampi Antonio 8 Greenwood Celia MT … - Nature, 2015 - nature.com
The contribution of rare and low-frequency variants to human traits is largely unexplored.
Here we describe insights from sequencing whole genomes (low read depth, 7×) or exomes …
Here we describe insights from sequencing whole genomes (low read depth, 7×) or exomes …
The UK10K project identifies rare variants in health and disease
K Walter, JL Min, J Huang, L Crooks - Nature, 2015 - shura.shu.ac.uk
The contribution of rare and low-frequency variants to human traits is largely unexplored.
Here we describe insights from sequencing whole genomes (low read depth, 73) or exomes …
Here we describe insights from sequencing whole genomes (low read depth, 73) or exomes …
The UK10K project identifies rare variants in health and disease
UK10K Consortium - Nature, 2015 - abdn.elsevierpure.com
The contribution of rare and low-frequency variants to human traits is largely unexplored.
Here we describe insights from sequencing whole genomes (low read depth, 7×) or exomes …
Here we describe insights from sequencing whole genomes (low read depth, 7×) or exomes …
The UK10K project identifies rare variants in health and disease
K Walter, JL Min, J Huang, L Crooks, Y Memari… - Nature, 2015 - eprints.ncl.ac.uk
The contribution of rare and low-frequency variants to human traits is largely unexplored.
Here we describe insights from sequencing whole genomes (low read depth, 7x) or exomes …
Here we describe insights from sequencing whole genomes (low read depth, 7x) or exomes …
The UK10K project identifies rare variants in health and disease
JRB Perry, JB Richards, G Clement, D Hart, P Hysi… - NATURE, 2015 - kclpure.kcl.ac.uk
The contribution of rare and low-frequency variants to human traits is largely unexplored.
Here we describe insights from sequencing whole genomes (low read depth, 7×) or exomes …
Here we describe insights from sequencing whole genomes (low read depth, 7×) or exomes …
The UK10K project identifies rare variants in health and disease
K Walter, JL Min, J Huang, L Crooks, Y Memari… - 2015 - ricerca.unityfvg.it
The contribution of rare and low-frequency variants to human traits is largely unexplored.
Here we describe insights from sequencing whole genomes (low read depth, 7×) or exomes …
Here we describe insights from sequencing whole genomes (low read depth, 7×) or exomes …
The UK10K project identifies rare variants in health and disease.
K Walter, J Min, J Huang, L Crooks, Y Memari… - NATURE, 2015 - iris.univr.it
The contribution of rare and low-frequency variants to human traits is largely unexplored.
Here we describe insights from sequencing whole genomes (low read depth, 7×) or exomes …
Here we describe insights from sequencing whole genomes (low read depth, 7×) or exomes …
[HTML][HTML] The UK10K project identifies rare variants in health and disease
K Walter, JL Min, J Huang, L Crooks, Y Memari… - Nature, 2015 - kups.ub.uni-koeln.de
The contribution of rare and low-frequency variants to human traits is largely unexplored.
Here we describe insights from sequencing whole genomes (low read depth, 7x) or exomes …
Here we describe insights from sequencing whole genomes (low read depth, 7x) or exomes …
The UK10K project identifies rare variants in health and disease
K Walter, J Min, J Huang, L Crooks, Y Memari… - NATURE, 2015 - iris.unical.it
The contribution of rare and low-frequency variants to human traits is largely unexplored.
Here we describe insights from sequencing whole genomes (low read depth, 7×) or exomes …
Here we describe insights from sequencing whole genomes (low read depth, 7×) or exomes …
The UK10K project identifies rare variants in health and disease
K Walter, JL Min, J Huang, L Crooks, Y Memari… - …, 2015 - researchportal.ukhsa.gov.uk
The contribution of rare and low-frequency variants to human traits is largely unexplored.
Here we describe insights from sequencing whole genomes (low read depth, 7×) or exomes …
Here we describe insights from sequencing whole genomes (low read depth, 7×) or exomes …