Add to ORKGRecent advances in sequencing technologies have made it possible for the first time to sequence and analyse the genomes of hundreds of individuals in both a cost-effective manner and in a reasonable amount of time. One of the primary applications of this data is to better understand and investigate the genetic basis of common phenotypes or diseases. Genome
Motivation: The sequencing of the human genome has made it possible to identify an informative set o...
With the availability of dense maps of anonymous and frequent SNPs spanning the whole human genome, ...
With the availability of dense maps of anonymous and frequent SNPs spanning the whole human genome, ...
The sequencing of the human genome1 and the subsequentcompletion of the human haplotype mapping (Hap...
Genome-wide association studies (GWASs) have had a tremendous impact on the pace of genomic research...
After more than a decade of hope and hype, researchers are finally making inroads into understanding...
Motivation: The sequencing of the human genome has made it possible to identify an informative set o...
Motivation: The sequencing of the human genome has made it possible to identify an informative set o...
For the past two decades, linkage analysis and genome-wide analysis have greatly advanced our knowle...
To fully understand the allelic variation that underlies common diseases, complete genome sequencing...
With the availability of dense maps of anonymous and frequent SNPs spanning the whole human genome, ...
When the time came to decide on the topic for the next in the series of Human Molecular Genetics rev...
With the availability of dense maps of anonymous and frequent SNPs spanning the whole human genome, ...
With the availability of dense maps of anonymous and frequent SNPs spanning the whole human genome, ...
With the availability of dense maps of anonymous and frequent SNPs spanning the whole human genome, ...
Motivation: The sequencing of the human genome has made it possible to identify an informative set o...
With the availability of dense maps of anonymous and frequent SNPs spanning the whole human genome, ...
With the availability of dense maps of anonymous and frequent SNPs spanning the whole human genome, ...
The sequencing of the human genome1 and the subsequentcompletion of the human haplotype mapping (Hap...
Genome-wide association studies (GWASs) have had a tremendous impact on the pace of genomic research...
After more than a decade of hope and hype, researchers are finally making inroads into understanding...
Motivation: The sequencing of the human genome has made it possible to identify an informative set o...
Motivation: The sequencing of the human genome has made it possible to identify an informative set o...
For the past two decades, linkage analysis and genome-wide analysis have greatly advanced our knowle...
To fully understand the allelic variation that underlies common diseases, complete genome sequencing...
With the availability of dense maps of anonymous and frequent SNPs spanning the whole human genome, ...
When the time came to decide on the topic for the next in the series of Human Molecular Genetics rev...
With the availability of dense maps of anonymous and frequent SNPs spanning the whole human genome, ...
With the availability of dense maps of anonymous and frequent SNPs spanning the whole human genome, ...
With the availability of dense maps of anonymous and frequent SNPs spanning the whole human genome, ...
Motivation: The sequencing of the human genome has made it possible to identify an informative set o...
With the availability of dense maps of anonymous and frequent SNPs spanning the whole human genome, ...
With the availability of dense maps of anonymous and frequent SNPs spanning the whole human genome, ...