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

Detecting structural variations in the human genome using next generation sequencing.

Briefings in functional genomics - 1 Dec 2010

Xi Ruibin, Kim Tae-Min, Park Peter J

Abstract excerpt

Structural variations are widespread in the human genome and can serve as genetic markers in clinical and evolutionary studies. With the advances in the next-generation sequencing technology, recent methods allow for identification of structural variations with unprecedented resolution and accuracy. They also provide opportunities to discover variants that could not be detected on conventional microarray-based...

Read the complete abstract on PubMed

Topics

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

Share to Algorithms
Share to Chromosome Mapping
Share to Genetic Markers

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Variation

Share to Genome, Human

Share to Sequence Analysis, DNA

Source

Open in PubMed Open full text

Identifiers

PMID: 21216738
DOI: 10.1093/bfgp/elq025
PMCID: PMC3080742

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Detecting structural variations in the human genome using next generation sequencing.PMID 21216738Read ↗

[Structural variation in the human genome].Semantic proximity Read ↗

Progress in the detection of human genome structural variations.Semantic proximity Read ↗

Mapping and sequencing of structural variation from eight human genomes.Semantic proximity Read ↗

Detection and interpretation of genomic structural variation in health and disease.Semantic proximity Read ↗

Genome-wide approaches and technologies to assess human variationSemantic proximity Read ↗

Genome structural variation discovery and genotyping.Semantic proximity Read ↗

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

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

Computational methods for discovering structural variation with next-generation sequencing.Semantic proximity Read ↗

A Practical Guide for Structural Variation Detection in the Human Genome.Semantic proximity Read ↗

Structural variation in the human genome.Semantic proximity Read ↗

Genomic sequencing in clinical trialsSemantic proximity Read ↗

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