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 scan statistic for identifying chromosomal patterns of SNP association.

Genetic epidemiology - 1 Nov 2006

Sun Yan V, Levin Albert M, Boerwinkle Eric, Robertson Henry, Kardia Sharon L R

Abstract excerpt

We have developed a single nucleotide polymorphism (SNP) association scan statistic that takes into account the complex distribution of the human genome variation in the identification of chromosomal regions with significant SNP associations. This scan statistic has wide applicability for genetic analysis, whether to identify important chromosomal regions associated with common diseases based on whole-genome SNP...

Read the complete abstract on PubMed

Topics

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

Share to Chromosome Mapping
Share to Chromosomes, Human
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Poisson Distribution

Share to Polymorphism, Single Nucleotide

Source

Identifiers

PMID: 16858698
DOI: 10.1002/gepi.20173

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

A scan statistic for identifying chromosomal patterns of SNP association.PMID 16858698Read ↗

Scan statistics to scan markers for susceptibility genes.Semantic proximity Read ↗

A 4-Mb high-density single nucleotide polymorphism-based map around human APOE.Semantic proximity Read ↗

Sequential haplotype scan methods for association analysis.Semantic proximity Read ↗

A tool for selecting SNPs for association studies based on observed linkage disequilibrium patterns.Semantic proximity Read ↗

Dynamic Scan Procedure for Detecting Rare-Variant Association Regions in Whole Genome Sequencing StudiesSemantic proximity Read ↗

A powerful and rapid approach to human genome scanning using small quantities of genomic DNA.Semantic proximity Read ↗

A scan statistic to extract causal gene clusters from case-control genome-wide rare CNV data.Semantic proximity Read ↗

Linkage disequilibrium maps constructed with common SNPs are useful for first-pass disease association screens.Semantic proximity Read ↗

A graphical assessment of p-values from sliding window haplotype tests of association to identify asthma susceptibility loci on chromosome 11q.Semantic proximity Read ↗

A genetic map of human chromosome 17p.Semantic proximity Read ↗

Ankylosing spondylitis susceptibility loci defined by genome-search meta-analysis.Semantic proximity Read ↗

Segment-wise genome-wide association analysis identifies a candidate region associated with schizophrenia in three independent samples.Semantic proximity Read ↗

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