ArticlePloS one2009
Visualization of shared genomic regions and meiotic recombination in high-density SNP data.
Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.
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Who cites it
20 citing papers in PubMed, 41 citations in OpenAlex.
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- Bio-collections in autism research.Molecular autism · 2017Review
- Genome-wide eQTLs and heritability for gene expression traits in unrelated individuals.BMC genomics · 2014Article
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- Identification of pedigree relationship from genome sharing.G3 (Bethesda, Md.) · 2013Article
- Mosaic segmental uniparental isodisomy and progressive clonal selection: a common mechanism of late onset β-thalassemia major.Haematologica · 2013Article
- Low frequency variants, collapsed based on biological knowledge, uncover complexity of population stratification in 1000 genomes project data.PLoS genetics · 2013Article
- Chromosomal variation in lymphoblastoid cell lines.Human mutation · 2012Article
- Consanguinity in Centre d'Étude du Polymorphisme Humain (CEPH) pedigrees.European journal of human genetics : EJHG · 2012Article
- Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities.Molecular cytogenetics · 2012Article
- Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing.Science translational medicine · 2012Article
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- Inference of relationships in population data using identity-by-descent and identity-by-state.PLoS genetics · 2011Article
- Analysis of human meiotic recombination events with a parent-sibling tracing approach.BMC genomics · 2011Article
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- Locations and patterns of meiotic recombination in two-generation pedigrees.BMC medical genetics · 2009Article
Corrections and comments
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Authors and funding
2 authors at 2 institutions in 1 country.
Funding
Abstract
backgroundA fundamental goal of single nucleotide polymorphism (SNP) genotyping is to determine the sharing of alleles between individuals across genomic loci. Such analyses have diverse applications in defining the relatedness of individuals (including unexpected relationships in nominally unrelated individuals, or consanguinity within pedigrees), analyzing meiotic crossovers, and identifying a broad range of chromosomal anomalies such as hemizygous deletions and uniparental disomy, and analyzing population structure. PRINCIPAL
findingsWe present SNPduo, a command-line and web accessible tool for analyzing and visualizing the relatedness of any two individuals using identity by state. Using identity by state does not require prior knowledge of allele frequencies or pedigree information, and is more computationally tractable and is less affected by population stratification than calculating identity by descent probabilities. The web implementation visualizes shared genomic regions, and generates UCSC viewable tracks. The command-line version requires pedigree information for compatibility with existing software and determining specified relationships even though pedigrees are not required for IBS calculation, generates no visual output, is written in portable C++, and is well-suited to analyzing large datasets. We demonstrate how the SNPduo web tool identifies meiotic crossover positions in siblings, and confirm our findings by visualizing meiotic recombination in synthetic three-generation pedigrees. We applied SNPduo to 210 nominally unrelated Phase I / II HapMap samples and, consistent with previous findings, identified six undeclared pairs of related individuals. We further analyzed identity by state in 2,883 individuals from multiplex families with autism and identified a series of anomalies including related parents, an individual with mosaic loss of chromosome 18, an individual with maternal heterodisomy of chromosome 16, and unexplained replicate samples.
conclusionsSNPduo provides the ability to explore and visualize SNP data to characterize the relatedness between individuals. It is compatible with, but distinct from, other established analysis software such as PLINK, and performs favorably in benchmarking studies for the analyses of genetic relatedness.
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