Evidence map›Paper›PMID 20438641›Full record

ArticleBMC bioinformatics2010

Partitioning of copy-number genotypes in pedigrees.

Louis-Philippe Lemieux Perreault, Gregor U Andelfinger, Géraldine Asselin, Marie-Pierre Dubé

Abstract read
In one paragraph

Article in BMC bioinformatics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Louis-Philippe Lemieux PerreaultMontreal Heart Institute Research Center, Montréal, Canada. louis-philippe.lemieux.perreault@umontreal.ca
Gregor U Andelfinger
Géraldine Asselin
Marie-Pierre Dubé

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

backgroundCopy number variations (CNVs) and polymorphisms (CNPs) have only recently gained the genetic community's attention. Conservative estimates have shown that CNVs and CNPs might affect more than 10% of the genome and that they may be at least as important as single nucleotide polymorphisms in assessing human variability. Widely used tools for CNP analysis have been implemented in Birdsuite and PLINK for the purpose of conducting genetic association studies based on the unpartitioned total number of CNP copies provided by the intensities from Affymetrix's Genome-Wide Human SNP Array. Here, we are interested in partitioning copy number variations and polymorphisms in extended pedigrees for the purpose of linkage analysis on familial data.

resultsWe have developed CNGen, a new software for the partitioning of copy number polymorphism using the integrated genotypes from Birdsuite with the Affymetrix platform. The algorithm applied to familial trios or extended pedigrees can produce partitioned copy number genotypes with distinct parental alleles. We have validated the algorithm using simulations on a complex pedigree structure using frequencies calculated from a real dataset of 300 genotyped samples from 42 pedigrees segregating a congenital heart defect phenotype.

conclusionsCNGen is the first published software for the partitioning of copy number genotypes in pedigrees, making possible the use CNPs and CNVs for linkage analysis. It was implemented with the Python interpreter version 2.5.2. It was successfully tested on current Linux, Windows and Mac OS workstations.

Indexed as

DNA Copy Number VariationsGenotypePedigreeGene DosageGenetic VariationHumansPhenotype

Identifiers

PMID20438641
PMCPMC2874807

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.