Coupling dense genotype data with new computational methods offers unprecedented opportunities for individual-level ancestry estimation once geographically precisely defined reference data sets become available. We study such a reference data set for Finland containing 2376 such individuals from the FINRISK Study survey of 1997 both of whose parents were born close to each other. This sampling strategy focuses on the population structure present in Finland before the 1950s. By using the recent haplotype-based methods ChromoPainter (CP) and FineSTRUCTURE (FS) we reveal a highly geographically clustered genetic structure in Finland and report its connections to the settlement history as well as to the current dialectal regions of the Finnish ...
Finnish samples have been extensively utilized in studying single-gene disorders, where the founder ...
SummaryThe Finnish population has often been viewed as an isolate founded 2,000 years ago via a rout...
Isolated populations have been valuable for the discovery of rare monogenic diseases and their causa...
Coupling dense genotype data with new computational methods offers unprecedented opportunities for i...
Information about individual-level genetic ancestry is central to population genetics, forensics and...
Information about individual-level genetic ancestry is central to population genetics, forensics and...
Information about individual-level genetic ancestry is central to population genetics, forensics and...
Finland provides unique opportunities to investigate population and medical genomics because of its ...
The Finnish population is a unique example of a genetic isolate affected by a recent founder event. ...
Genome-wide data provide a powerful tool for inferring patterns of genetic variation and structure o...
Although high-density SNP genotyping platforms generate a momentum for detailed genome-wide associat...
Andrew Hattersley and T Frayling were collaborators on this journal article/project.Finnish samples ...
Finnish samples have been extensively utilized in studying single-gene disorders, where the founder ...
Finnish samples have been extensively utilized in studying single-gene disorders, where the founder ...
Although high-density SNP genotyping platforms generate a momentum for detailed genome-wide associat...
Finnish samples have been extensively utilized in studying single-gene disorders, where the founder ...
SummaryThe Finnish population has often been viewed as an isolate founded 2,000 years ago via a rout...
Isolated populations have been valuable for the discovery of rare monogenic diseases and their causa...
Coupling dense genotype data with new computational methods offers unprecedented opportunities for i...
Information about individual-level genetic ancestry is central to population genetics, forensics and...
Information about individual-level genetic ancestry is central to population genetics, forensics and...
Information about individual-level genetic ancestry is central to population genetics, forensics and...
Finland provides unique opportunities to investigate population and medical genomics because of its ...
The Finnish population is a unique example of a genetic isolate affected by a recent founder event. ...
Genome-wide data provide a powerful tool for inferring patterns of genetic variation and structure o...
Although high-density SNP genotyping platforms generate a momentum for detailed genome-wide associat...
Andrew Hattersley and T Frayling were collaborators on this journal article/project.Finnish samples ...
Finnish samples have been extensively utilized in studying single-gene disorders, where the founder ...
Finnish samples have been extensively utilized in studying single-gene disorders, where the founder ...
Although high-density SNP genotyping platforms generate a momentum for detailed genome-wide associat...
Finnish samples have been extensively utilized in studying single-gene disorders, where the founder ...
SummaryThe Finnish population has often been viewed as an isolate founded 2,000 years ago via a rout...
Isolated populations have been valuable for the discovery of rare monogenic diseases and their causa...