Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Overview of structural variation calling: Simulation, identification, and visualization.

Computers in biology and medicine - 1 Jun 2022

Lei Yu, Meng Yue, Guo Xinqi, Ning Ke, Bian Yixin, Li Lanlan, Hu Zhenduo, Anashkina Anastasia A, Jiang Qinghua, Dong Yucui, Zhu Xiao

Abstract excerpt

Structural variation (SV) is a vital part of biological genetic diversity. The simulation and identification with high efficiency and accuracy are considered to be very important. With the continuous development and wide application of various technologies, computer simulation of genomic data has attracted wide attention due to its intuitive and convenient advantages. Meanwhile, there are several high-quality...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Computer Simulation
Share to Genetic Variation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome, Human

Share to Genomic Structural Variation

Share to Genomics

Share to High-Throughput Nucleotide Sequencing

Share to Sequence Analysis, DNA

Source

Identifiers

PMID: 35585730
DOI: 10.1016/j.compbiomed.2022.105534

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Overview of structural variation calling: Simulation, identification, and visualization.PMID 35585730Read ↗

Visualization tools for human structural variations identified by whole-genome sequencing.Semantic proximity Read ↗

Complex structural variant visualization with SVTopoSemantic proximity Read ↗

MagicViewer: integrated solution for next-generation sequencing data visualization and genetic variation detection and annotation.Semantic proximity Read ↗

Publication-ready single nucleotide polymorphism visualization with snipit.Semantic proximity Read ↗

VisVariant: A java program to visualise genetic variants in next-generation sequencing dataSemantic proximity Read ↗

Correspondence on NanoVar's performance outlined by Jiang T. et al. in "Long-read sequencing settings for efficient structural variation detection based on comprehensive evaluation".Semantic proximity Read ↗

SVbyEye: A visual tool to characterize structural variation among whole-genome assembliesSemantic proximity Read ↗

A benchmark of structural variation detection by long reads through a realistic simulated modelSemantic proximity Read ↗

svviz: a read viewer for validating structural variants.Semantic proximity Read ↗

BioJS-HGV Viewer: Genetic Variation VisualizerSemantic proximity Read ↗

MapView: visualization of short reads alignment on a desktop computer.Semantic proximity Read ↗

Evaluation of computational genotyping of Structural Variations for clinical diagnosesSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.