Article

Genome-wide Copy Number Variations in a Large Cohort of Bantu African Children

2020-12-24

Abstract excerpt

<h4>Background</h4> Copy number variations (CNVs) account for a substantial proportion of inter-individual genomic variation. However, a majority of genomic variation studies have focused on single-nucleotide variations (SNVs), with limited genome-wide analysis of CNVs in large cohorts, especially in populations that are under-represented in genetic studies including people of African descent. <h4>Results</h4> I...

Topics

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

Identifiers and source

Literature Corpus work: 55b67eb1-2b6a-5b3a-af9c-96127c07dc51
DOI: 10.1101/2020.12.24.424207

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Genome-wide Copy Number Variations in a Large Cohort of Bantu African ChildrenDOI 10.1101/2020.12.24.424207Read

Copy number variation in human genomes from three major ethno-linguistic groups in Africa.Semantic proximity Read

High resolution discovery and confirmation of copy number variants in 90 Yoruba Nigerians.Semantic proximity Read

DNA copy number variation: Main characteristics, evolutionary significance, and pathological aspectsSemantic proximity Read

Global variation in copy number in the human genome.Semantic proximity Read

Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations.Semantic proximity Read

Copy number variations in the human genome and strategies for analysis.Semantic proximity Read

Copy Number Variant analysis by exome sequencing is an effective approach to optimize diagnostic yield for developmental disorders – the DDD-Africa studySemantic proximity Read

The individual and global impact of copy number variants on complex human traitsSemantic proximity Read

Copy number variation in human health, disease, and evolution.Semantic proximity Read

Copy number variation in African Americans.Semantic proximity Read

Implications of gene copy-number variation in health and diseases.Semantic proximity Read

Microarray-based maps of copy-number variant regions in European and sub-Saharan populations.Semantic proximity Read