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

PedSplit: pedigree management for stratified analysis.

Bioinformatics (Oxford, England) - 22 Sept 2004

Lanktree M B, VanderBeek L, Macciardi F M, Kennedy J L

Abstract excerpt

SUMMARY: PedSplit facilitates pedigree management for gene-gene interaction and sex specific tests for increased homogeneity within subgroups. PedSplit also provides a simple approach for calculating haplotype relative risk and generating internal 'controls'. AVAILABILITY: Executables, C++ source code and documentation for PedSplit can be downloaded from http://www.pharmacogenetics.ca in the links and software...

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 Genetic Testing

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Internet

Share to Linkage Disequilibrium

Share to Risk Assessment

Share to Sex Factors

Share to Software

Source

Identifiers

PMID: 15059823
DOI: 10.1093/bioinformatics/bth224

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

PedSplit: pedigree management for stratified analysis.PMID 15059823Read ↗

Population Stratification at the Phenotypic Variance level and Implication for the Analysis of Whole Genome Sequencing Data from Multiple StudiesSemantic proximity Read ↗

Software Application Profile: RVPedigree: a suite of family-based rare variant association tests for normally and non-normally distributed quantitative traits.Semantic proximity Read ↗

Pedigree Selection and Information Content.Semantic proximity Read ↗

BayesMendel: an R Environment for Mendelian Risk PredictionSemantic proximity Read ↗

SimRVSequences: an R package to simulate genetic sequence data for pedigreesSemantic proximity Read ↗

<i>KinformR</i>: novel pedigree and candidate variant scoring methods for family-based genetic studiesSemantic proximity Read ↗

PedGenie: meta genetic association testing in mixed family and case-control designs.Semantic proximity Read ↗

Sex differences in genetic architecture in the UK Biobank.Semantic proximity Read ↗

PleioGRiP: genetic risk prediction with pleiotropy.Semantic proximity Read ↗

A tutorial on statistical methods for population association studies.Semantic proximity Read ↗

What are SNPs and haplotypes and how will they help us manage the prevention of adult cancer?Semantic proximity Read ↗

Genome-wide complex trait analysis (GCTA): methods, data analyses, and interpretations.Semantic proximity Read ↗

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