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

Detection and integration of genotyping errors in statistical genetics.

American journal of human genetics - 1 Feb 2002

Sobel Eric, Papp Jeanette C, Lange Kenneth

Abstract excerpt

Detection of genotyping errors and integration of such errors in statistical analysis are relatively neglected topics, given their importance in gene mapping. A few inopportunely placed errors, if ignored, can tremendously affect evidence for linkage. The present study takes a fresh look at the calculation of pedigree likelihoods in the presence of genotyping error. To accommodate genotyping error, we present...

Read the complete abstract on PubMed

Topics

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

Share to Founder Effect
Share to Markov Chains
Share to Monte Carlo Method

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Paternity

Share to Research Design

Share to Software

Share to Stochastic Processes

Source

Open in PubMed Open full text

Identifiers

PMID: 11791215
DOI: 10.1086/338920
PMCID: PMC384922

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. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Detection and integration of genotyping errors in statistical genetics.PMID 11791215Read ↗

Simultaneous estimation of genotype error and uncalled deletion rates in whole genome sequence dataSemantic proximity Read ↗

Integration of SNP genotyping confidence scores in IBD inference.Semantic proximity Read ↗

Genotyping errors: causes, consequences and solutions.Semantic proximity Read ↗

Simultaneous estimation of genotype error and uncalled deletion rates in whole genome sequence data.Semantic proximity Read ↗

A multipoint method for detecting genotyping errors and mutations in sibling-pair linkage data.Semantic proximity Read ↗

An optimal algorithm for automatic genotype elimination.Semantic proximity Read ↗

Detecting Pedigree Relationship Errors.Semantic proximity Read ↗

Distinct error rates for reference and nonreference genotypes estimated by pedigree analysis.Semantic proximity Read ↗

Genotyping errors and their impact on genetic analysis.Semantic proximity Read ↗

Detecting pedigree relationship errors.Semantic proximity Read ↗

Detection of Mendelian consistent genotyping errors in pedigrees.Semantic proximity Read ↗

Inferring haplotypes and parental genotypes in larger full sib-ships and other pedigrees with missing or erroneous genotype data.Semantic proximity Read ↗

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