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 of Mendelian consistent genotyping errors in pedigrees.

Genetic epidemiology - 1 May 2014

Cheung Charles Y K, Thompson Elizabeth A, Wijsman Ellen M

Abstract excerpt

Detection of genotyping errors is a necessary step to minimize false results in genetic analysis. This is especially important when the rate of genotyping errors is high, as has been reported for high-throughput sequence data. To detect genotyping errors in pedigrees, Mendelian inconsistent (MI) error checks exist, as do multi-point methods that flag Mendelian consistent (MC) errors for sparse multi-allelic...

Read the complete abstract on PubMed

Topics

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

Share to Polymorphism, Single Nucleotide
Share to Research Design
Share to Alleles

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

Share to Genotype

Share to Genotyping Techniques

Share to Markov Chains

Share to Monte Carlo Method

Share to Pedigree

Source

Open in PubMed Open full text

Identifiers

PMID: 24718985
DOI: 10.1002/gepi.21806
PMCID: PMC4081466

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 of Mendelian consistent genotyping errors in pedigrees.PMID 24718985Read ↗

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

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

GIGI: an approach to effective imputation of dense genotypes on large pedigrees.Semantic proximity Read ↗

Evaluating power and type 1 error in large pedigree analyses of binary traits.Semantic proximity Read ↗

Haplotype inference in general pedigrees using the cluster variation method.Semantic proximity Read ↗

Detection and integration of genotyping errors in statistical genetics.Semantic proximity Read ↗

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

Comparative study of multipoint methods for genotype error detection.Semantic proximity Read ↗

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

Detecting Pedigree Relationship Errors.Semantic proximity Read ↗

A statistical framework to guide sequencing choices in pedigrees.Semantic proximity Read ↗

Detecting pedigree relationship errors.Semantic proximity Read ↗

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