Article

DNA sequence features underlying large-scale duplications and deletions in human

2021-04-26

Abstract excerpt

<title>Abstract</title> <p><bold>Background</bold>Copy Number Variants (CNVs) may cover up to 12% of the whole genome and have substantial impact on phenotypes. We used 5 867 duplications and 33 181 deletions available from the <italic>1000 Genomes Project</italic> to characterize genomic regions vulnerable to CNV formation and to identify sequence features characteristic for those regions.<bold>Results</bold>Onl...

Topics

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

Identifiers and source

Literature Corpus work: 2c63ea0f-ac17-5687-a2df-3e33cf64e269
DOI: 10.21203/rs.3.rs-458335/v1

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

DNA sequence features underlying large-scale duplications and deletions in humanDOI 10.21203/rs.3.rs-458335/v1Read

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

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

Mutational and selective effects on copy-number variants in the human genome.Semantic proximity Read

Copy-Number Variations, Noncoding Sequences, and Human PhenotypesSemantic proximity Read

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

[Copy number variations in the human genome: their mutational mechanisms and roles in diseases].Semantic proximity Read

[Association of common copy number variations with diseases].Semantic proximity Read

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

Copy Number Variation.Semantic proximity Read

Copy number variation: new insights in genome diversity.Semantic proximity Read

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

The discovery of human genetic variations and their use as disease markers: past, present and future.Semantic proximity Read