Pedigrees, or family trees, are directed graphs used to identify sites of the genome that are correlated with the presence or absence of a disease. With the advent of genotyping and sequencing technologies, there has been an explosion in the amount of data available, both in the number of individuals and in the number of sites. Some pedigrees number in the thousands of individuals. Meanwhile, analysis methods have remained limited to pedigrees of < 100 individuals which limits analyses to many small independent pedigrees. Disease models, such those used for the linkage analysis log-odds (LOD) estima-tor, have similarly been limited. This is because linkage analysis was originally designed with a different task in mind, that of ordering t...
Large-scale association studies are being undertaken with the hope of uncovering the genetic determi...
Background: Pedigree studies of complex heritable diseases often feature nominal or ordinal phenotyp...
As the extent of human genetic variation becomes more fully characterized, the research community is...
Inference of pedigrees from genetic data is a fundamental problem in the field of population genetic...
Inference of pedigrees from genetic data is a fundamental problem in the field of population genetic...
Pedigree studies of complex heritable diseases often feature nominal or ordinal phenotypic measureme...
Pedigree studies of complex heritable diseases often feature nominal or ordinal phenotypic measureme...
Pedigree studies of complex heritable diseases often feature nominal or ordinal phenotypic measureme...
Analyses of genetic data on groups of related individuals, or pedigrees, frequently require the calc...
We present a method for improving the power of linkage analysis by detecting chromosome segments sha...
Motivation: The emphasis of genetic linkage anal-ysis is rapidly shifting from the task of locating ...
Abstract Background In the last years GWA studies have successfully identified common SNPs associate...
Background In the last years GWA studies have successfully identified common SNPs associated with c...
BACKGROUND: In the last years GWA studies have successfully identified common SNPs associated with c...
Large-scale association studies are being undertaken with the hope of uncovering the genetic determi...
Large-scale association studies are being undertaken with the hope of uncovering the genetic determi...
Background: Pedigree studies of complex heritable diseases often feature nominal or ordinal phenotyp...
As the extent of human genetic variation becomes more fully characterized, the research community is...
Inference of pedigrees from genetic data is a fundamental problem in the field of population genetic...
Inference of pedigrees from genetic data is a fundamental problem in the field of population genetic...
Pedigree studies of complex heritable diseases often feature nominal or ordinal phenotypic measureme...
Pedigree studies of complex heritable diseases often feature nominal or ordinal phenotypic measureme...
Pedigree studies of complex heritable diseases often feature nominal or ordinal phenotypic measureme...
Analyses of genetic data on groups of related individuals, or pedigrees, frequently require the calc...
We present a method for improving the power of linkage analysis by detecting chromosome segments sha...
Motivation: The emphasis of genetic linkage anal-ysis is rapidly shifting from the task of locating ...
Abstract Background In the last years GWA studies have successfully identified common SNPs associate...
Background In the last years GWA studies have successfully identified common SNPs associated with c...
BACKGROUND: In the last years GWA studies have successfully identified common SNPs associated with c...
Large-scale association studies are being undertaken with the hope of uncovering the genetic determi...
Large-scale association studies are being undertaken with the hope of uncovering the genetic determi...
Background: Pedigree studies of complex heritable diseases often feature nominal or ordinal phenotyp...
As the extent of human genetic variation becomes more fully characterized, the research community is...