Evidence map›Paper›PMID 19642289›Full record

ArticleComputational systems bioinformatics. Computational Systems Bioinformatics Conference2008

Efficient haplotype inference from pedigrees with missing data using linear systems with disjoint-set data structures.

Xin Li, Jing Li

Abstract read
In one paragraph

Article in Computational systems bioinformatics. Computational Systems Bioinformatics Conference, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Xin LiDepartment of Electrical Engineering and Computer Science, Case Western Reserve University, Cleveland, OH 44106, USA.
Jing Li

Funding

FAMILIAL AND BIRTH COHORT EFFECTS ON THE AGING SENSESR01AG021917 · NIA · UNIVERSITY OF WISCONSIN-MADISON · PI CRUICKSHANKS, KAREN J · 2004 to 2018
$25.2M
X-LINKED EXTENSION OF THE REVISED HASEMAN-ELSTON ALGORITHM FOR LINKAGE ANALYSISP41RR003655 · NCRR · LOUISIANA STATE UNIV HSC NEW ORLEANS · PI ELSTON, ROBERT C. · 1987 to 2011
$11.5M
GENETIC ANALYSIS OF COMMON DISEASES: AN EVALUATIONR01GM031575 · NIGMS · UNIVERSITY OF TEXAS RIO GRANDE VALLEY · PI ALMASY, LAURA A. · 1985 to 2016
$7.8M
Multi-point and multi-locus analysis of genomic association dataR01LM008991 · NLM · CASE WESTERN RESERVE UNIVERSITY · PI LI, JING · 2006 to 2010
$3.1M
Investigation of the Genetics of AsthmaR01HL049609 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLUMENTHAL, MALCOLM NOLAN · 2003 to 2006
$3.1M
NCRR NIH HHS P41 RR003655NCRR NIH HHS RR03655NHLBI NIH HHS 5R01-HL49609-14NHLBI NIH HHS R01 HL049609NIA NIH HHS 1R01-AG021917-01A1NIA NIH HHS R01 AG021917NIGMS NIH HHS R01 GM031575NLM NIH HHS LM008991NLM NIH HHS R01 LM008991
6 · The paper itself

Abstract

We study the haplotype inference problem from pedigree data under the zero recombination assumption, which is well supported by real data for tightly linked markers (i.e., single nucleotide polymorphisms (SNPs)) over a relatively large chromosome segment. We solve the problem in a rigorous mathematical manner by formulating genotype constraints as a linear system of inheritance variables. We then utilize disjoint-set structures to encode connectivity information among individuals, to detect constraints from genotypes, and to check consistency of constraints. On a tree pedigree without missing data, our algorithm can output a general solution as well as the number of total specific solutions in a nearly linear time O (mn x alpha(n)), where m is the number of loci, n is the number of individuals and alpha is the inverse Ackermann function, which is a further improvement over existing ones. We also extend the idea to looped pedigrees and pedigrees with missing data by considering existing (partial) constraints on inheritance variables. The algorithm has been implemented in C++ and will be incorporated into our PedPhase package. Experimental results show that it can correctly identify all 0-recombinant solutions with great efficiency. Comparisons with other two popular algorithms show that the proposed algorithm achieves 10 to 10(5)-fold improvements over a variety of parameter settings. The experimental study also provides empirical evidences on the complexity bounds suggested by theoretical analysis.

Indexed as

Databases, GeneticModels, GeneticPedigreeBase SequenceChromosome MappingComputer SimulationHaplotypesInformation Storage and RetrievalLinear ModelsMolecular Sequence DataSequence Analysis, DNA

Identifiers

PMID19642289
PMCPMC3326667

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Registered trials

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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.