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

An algorithm for inferring complex haplotypes in a region of copy-number variation.

American journal of human genetics - 1 Aug 2008

Kato Mamoru, Nakamura Yusuke, Tsunoda Tatsuhiko

Abstract excerpt

Recent studies have extensively examined the large-scale genetic variants in the human genome known as copy-number variations (CNVs), and the universality of CNVs in normal individuals, along with their functional importance, has been increasingly recognized. However, the absence of a method to accurately infer alleles or haplotypes within a CNV region from high-throughput experimental data hampers the finer...

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 Computer Simulation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Techniques

Share to Genome, Human

Share to Models, Genetic

Share to Models, Statistical

Share to Software

Source

Open in PubMed Open full text

Identifiers

PMID: 18639202
DOI: 10.1016/j.ajhg.2008.06.021
PMCID: PMC2495074

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

An algorithm for inferring complex haplotypes in a region of copy-number variation.PMID 18639202Read ↗

Influences of rare copy-number variation on human complex traits.Semantic proximity Read ↗

MOCSphaser: a haplotype inference tool from a mixture of copy number variation and single nucleotide polymorphism data.Semantic proximity Read ↗

Influences of rare copy number variation on human complex traitsSemantic proximity Read ↗

cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVs.Semantic proximity Read ↗

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

Haplotype phasing and inheritance of copy number variants in nuclear families.Semantic proximity Read ↗

Genotype, haplotype and copy-number variation in worldwide human populations.Semantic proximity Read ↗

Population-genetic nature of copy number variations in the human genome.Semantic proximity Read ↗

Inference of chromosome-specific copy numbers using population haplotypes.Semantic proximity Read ↗

Large multiallelic copy number variations in humans.Semantic proximity Read ↗

Analysis of Population-Genetic Properties of Copy Number Variations.Semantic proximity Read ↗

Integrated detection and population-genetic analysis of SNPs and copy number variation.Semantic proximity Read ↗

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