Recent research into structural variants (SVs) has established their importance to medicine and molecular biology, elucidating their role in various diseases, regulation of gene expression, ethnic diversity, and large-scale chromosome evolution-giving rise to the differences within populations and among species. Nevertheless, characterizing SVs and determining the optimal approach for a given experimental design remains a computational and scientific challenge. Multiple approaches have emerged to target various SV classes, zygosities, and size ranges. Here, we review these approaches with respect to their ability to infer SVs across the full spectrum of large, complex variations and present computational methods for each approach
Structural variations (SV) are broadly defined as genomic alterations that affect >50 bp of DNA, whi...
Structural variants (SVs) rearrange large segments of DNA(1) and can have profound consequences in e...
Genomic structural variants (SVs) are abundant in humans, differing from other forms of variation in...
Structural variants are implicated in numerous diseases and make up the majority of varying nucleoti...
Recent advances in long-read sequencing have given us an unprecedented view of structural variants (...
Structural variant (SV) differences between human genomes can cause germline and mosaic disease as w...
Chromosomal Structural Variation (SV) such as translocations, inversions, deletions, and duplicatio...
Comparison of human genomes shows that along with single nucleotide polymorphisms and small indels, ...
Structural variants (SVs) rearrange large segments of DNA1 and can have profound consequences in evo...
<div><p>Differences between individual human genomes, or between human and cancer genomes, range in ...
The incomplete identification of structural variants (SVs) from whole-genome sequencing data limits ...
Structural variants (SVs) are large insertions, deletions, duplications, inversions or translocation...
In the past decade, the view on genomic structural variation (SV) has been changed completely. SVs, ...
Structural and quantitative chromosomal rearrangements, collectively referred to as structural varia...
Motivation: Structural variants are defined as genomic variants larger than 50bp. They have been sho...
Structural variations (SV) are broadly defined as genomic alterations that affect >50 bp of DNA, whi...
Structural variants (SVs) rearrange large segments of DNA(1) and can have profound consequences in e...
Genomic structural variants (SVs) are abundant in humans, differing from other forms of variation in...
Structural variants are implicated in numerous diseases and make up the majority of varying nucleoti...
Recent advances in long-read sequencing have given us an unprecedented view of structural variants (...
Structural variant (SV) differences between human genomes can cause germline and mosaic disease as w...
Chromosomal Structural Variation (SV) such as translocations, inversions, deletions, and duplicatio...
Comparison of human genomes shows that along with single nucleotide polymorphisms and small indels, ...
Structural variants (SVs) rearrange large segments of DNA1 and can have profound consequences in evo...
<div><p>Differences between individual human genomes, or between human and cancer genomes, range in ...
The incomplete identification of structural variants (SVs) from whole-genome sequencing data limits ...
Structural variants (SVs) are large insertions, deletions, duplications, inversions or translocation...
In the past decade, the view on genomic structural variation (SV) has been changed completely. SVs, ...
Structural and quantitative chromosomal rearrangements, collectively referred to as structural varia...
Motivation: Structural variants are defined as genomic variants larger than 50bp. They have been sho...
Structural variations (SV) are broadly defined as genomic alterations that affect >50 bp of DNA, whi...
Structural variants (SVs) rearrange large segments of DNA(1) and can have profound consequences in e...
Genomic structural variants (SVs) are abundant in humans, differing from other forms of variation in...