Article

GCAT|Panel, a comprehensive structural variant haplotype map of the Iberian population from high-coverage whole-genome sequencing

2021-07-21

Abstract excerpt

<h4>ABSTRACT</h4> The combined analysis of haplotype panels with phenotype clinical cohorts is a common approach to explore the genetic architecture of human diseases. However, genetic studies are mainly based on single nucleotide variants (SNVs) and small insertions and deletions (indels). Here, we contribute to fill this gap by generating a dense haplotype map focused on the identification, characterization and...

Topics

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

Identifiers and source

Literature Corpus work: 1106d1fc-bcfe-575b-bc3d-3aa2926be5dc
DOI: 10.1101/2021.07.20.453041

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

GCAT|Panel, a comprehensive structural variant haplotype map of the Iberian population from high-coverage whole-genome sequencingDOI 10.1101/2021.07.20.453041Read

GCAT|Panel, a comprehensive structural variant haplotype map of the Iberian population from high-coverage whole-genome sequencing.Semantic proximity Read

An integrated map of genetic variation from 1,092 human genomes.Semantic proximity Read

Structural variants in Chinese population and their impact on phenotypes, diseases and population adaptationSemantic proximity Read

The Iberian Roma genetic variant server; population structure, susceptibility to disease and adaptive traitsSemantic proximity Read

al mena: a comprehensive resource of human genetic variants integrating genomes and exomes from Arab, Middle Eastern and North African populations.Semantic proximity Read

An integrated map of structural variation in 2,504 human genomes.Semantic proximity Read

High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios.Semantic proximity Read

Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil)Semantic proximity Read

Whole-genome sequencing of half-a-million UK Biobank participantsSemantic proximity Read

Whole-genome sequencing of 1,171 elderly admixed individuals from the largest Latin American metropolis (São Paulo, Brazil)Semantic proximity Read

Multi-platform discovery of haplotype-resolved structural variation in human genomesSemantic proximity Read

A high-quality human reference panel reveals the complexity and distribution of genomic structural variants.Semantic proximity Read