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

A definitive haplotype map as determined by genotyping duplicated haploid genomes finds a predominant haplotype preference at copy-number variation events.

American journal of human genetics - 11 Jun 2010

Kukita Yoji, Yahara Koji, Tahira Tomoko, Higasa Koichiro, Sonoda Miki, Yamamoto Ken, Kato Kiyoko, Wake Norio, Hayashi Kenshi

Abstract excerpt

The majority of complete hydatidiform moles (CHMs) harbor duplicated haploid genomes that originate from sperm. This makes CHMs more advantageous than conventional diploid cells for determining haplotypes of SNPs and copy-number variations (CNVs), because all of the genetic variants in a CHM geno...

Read the complete abstract on PubMed

Topics

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

Share to Aneuploidy
Share to Databases as Topic
Share to DNA Copy Number Variations

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Haploidy

Share to Haplotypes

Share to Hydatidiform Mole

Share to Nucleic Acid Hybridization

Share to Pregnancy

Source

Open in PubMed Open full text

Identifiers

PMID: 20537301
DOI: 10.1016/j.ajhg.2010.05.003
PMCID: PMC3032077

Genes

CHM

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20537301-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A definitive haplotype map as determined by genotyping duplicated haploid genomes finds a predominant haplotype preference at copy-number variation events.PMID 20537301Read ↗

D-HaploDB: a database of definitive haplotypes determined by genotyping complete hydatidiform mole samples.Semantic proximity Read ↗

Genome-wide definitive haplotypes determined using a collection of complete hydatidiform moles.Semantic proximity Read ↗

An algorithm for inferring complex haplotypes in a region of copy-number variation.Semantic proximity Read ↗

Complete and haplotype-resolved maps of genomic and epigenetic discordance in monozygotic twinsSemantic proximity Read ↗

T2T-YAO: a Telomere-to-telomere Assembled Diploid Reference Genome for Han ChineseSemantic proximity Read ↗

Single haplotype assembly of the human genome from a hydatidiform moleSemantic proximity Read ↗

Paternal origins of complete hydatidiform moles proven by whole genome single-nucleotide polymorphism haplotyping.Semantic proximity Read ↗

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

HaplotypeCN: copy number haplotype inference with Hidden Markov Model and localized haplotype clustering.Semantic proximity Read ↗

Genetic structures of copy number variants revealed by genotyping single sperm.Semantic proximity Read ↗

Single haplotype assembly of the human genome from a hydatidiform mole.Semantic proximity Read ↗

Linkage disequilibrium and heritability of copy-number polymorphisms within duplicated regions of the human genome.Semantic proximity Read ↗

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