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

Genome-wide profiling of structural genomic variations in Korean HapMap individuals.

PloS one - 2 Jul 2010

Bae Joon Seol, Cheong Hyun Sub, Park Byung Lae, Kim Lyoung Hyo, Han Chang Soo, Park Tae Joon, Kim Jason Yongha, Pasaje Charisse Flerida A, Lee Jin Sol, Shin Hyoung Doo

Abstract excerpt

BACKGROUND: Structural genomic variation study, along with microarray technology development has provided many genomic resources related with architecture of human genome, and led to the fact that human genome structure is a lot more complicated than previously thought. METHODOLOGY/PRINCIPAL FINDINGS: In the case of International HapMap Project, Epstein-Barr various immortalized cell lines were preferably used...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Asian People

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cell Line

Share to Chromosome Aberrations

Share to Genome, Human

Share to Genomic Structural Variation

Share to Loss of Heterozygosity

Share to Polymerase Chain Reaction

Source

Open in PubMed Open full text

Identifiers

PMID: 20625389
DOI: 10.1371/journal.pone.0011417
PMCID: PMC2896390

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

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

Genome-wide profiling of structural genomic variations in Korean HapMap individuals.PMID 20625389Read ↗

A comprehensive profile of DNA copy number variations in a Korean population: identification of copy number invariant regions among Koreans.Semantic proximity Read ↗

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

KGVDB: a population-based genomic map of CNVs tagged by SNPs in Koreans.Semantic proximity Read ↗

Copy number variations (CNVs) identified in Korean individuals.Semantic proximity Read ↗

Global patterns of large copy number variations in the human genome reveal complexity in chromosome organization.Semantic proximity Read ↗

A genome-wide survey of copy number variations in Han Chinese residing in Taiwan.Semantic proximity Read ↗

Array-Based Comparative Genomic Hybridization (aCGH).Semantic proximity Read ↗

Fine-scale map of encyclopedia of DNA elements regions in the Korean population.Semantic proximity Read ↗

Spectrum of large copy number variations in 26 diverse Indian populations: potential involvement in phenotypic diversity.Semantic proximity Read ↗

Compilation of copy number variants identified in phenotypically normal and parous Japanese women.Semantic proximity Read ↗

Whole genome distribution and ethnic differentiation of copy number variation in Caucasian and Asian populations.Semantic proximity Read ↗

The genetic effect of copy number variations on the risk of type 2 diabetes in a Korean population.Semantic proximity Read ↗

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