Article

FarGen: Elucidating the distribution of coding variants in the isolated population of the Faroe Islands

2022-06-17

Abstract excerpt

<title>Abstract</title> <p>Here we present results from FarGen Phase I exomes. This dataset is based on the FarGen cohort, which consists of 1,541 individuals from the isolated population of the Faroe Islands. The purpose of this cohort is to serve as a reference catalog of coding variants, and to conduct population genetic studies to better understand the genetic contribution to various diseases in the Faroese p...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 262d1a08-652a-5e95-b537-5409656157ac
DOI: 10.21203/rs.3.rs-1744790/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

FarGen: Elucidating the distribution of coding variants in the isolated population of the Faroe IslandsDOI 10.21203/rs.3.rs-1744790/v1Read

Faroese whole genomes provide insight into ancestry and recent selection.Semantic proximity Read

Evolution and functional impact of rare coding variation from deep sequencing of human exomes.Semantic proximity Read

Understanding local population genetics improves variant interpretation in rare genetic disordersSemantic proximity Read

Expanding CIRdb, a comprehensive catalog of whole-exome sequencing data of Canary IslandersSemantic proximity Read

The impact of the Turkish (TK) population variome on the genomic architecture of rare disease traitsSemantic proximity Read

Large-scale whole-genome sequencing of the Icelandic population.Semantic proximity Read

Whole-exome sequencing reveals a rapid change in the frequency of rare functional variants in a founding population of humans.Semantic proximity Read

Middle Eastern Genetic Variation Improves Clinical Annotation of the Human GenomeSemantic proximity Read

The functional spectrum of low-frequency coding variation.Semantic proximity Read

Characterization of Arabian Peninsula whole exomes: exploring high inbreeding featuresSemantic proximity Read

SNP heterozygosity, relatedness and inbreeding of whole genomes from the isolated population of the Faroe Islands.Semantic proximity Read

Long read sequencing of 3,622 Icelanders provides insight into the role of structural variants in human diseases and other traitsSemantic proximity Read