Evidence map›Paper›PMID 21610749›Full record

ArticleEuropean journal of human genetics : EJHG2011

Finding disease genes: a fast and flexible approach for analyzing high-throughput data.

William C L Stewart, Esther N Drill, David A Greenberg

Abstract readEvaluation Study
In one paragraph

Article in European journal of human genetics : EJHG, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. 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

3 authors.

William C L StewartDivision of Statistical Genetics, Department of Biostatistics, Mailman School of Public Health, Columbia University, New York, NY 10032, USA. ws2267@columbia.edu
Esther N Drill
David A Greenberg

Funding

RESOLVING HETEROGENEITY IN EPILEPSY WITH GENETIC MARKERSR01NS027941 · NINDS · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI GREENBERG, DAVID A. · 1990 to 2010
$9.0M
Mechanisms of Genetic Seizure Susceptibility in Juvenile Myoclonic EpilepsyR01NS061829 · NINDS · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI GREENBERG, DAVID A. · 2009 to 2012
$2.0M
Genetic Analysis: Psychiatric and Other Complex DiseasesT32MH065213 · NIMH · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI WEISSMAN, MYRNA M · 2002 to 2011
$1.7M
PSYCHIATRIC GENETICS AND FAMILY STUDIES--ROBUST METHODSR01MH048858 · NIMH · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI HODGE, SUSAN E. · 1992 to 2010
$1.5M
The Role of Genome-Coded ME2 in EpilepsyR21NS070323 · NINDS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GREENBERG, DAVID A. · 2009 to 2010
$798k
NIDA NIH HHS DA026983NIMH NIH HHS MH48858NIMH NIH HHS MH65213NIMH NIH HHS R01 MH048858NIMH NIH HHS T32 MH065213NINDS NIH HHS NS070323NINDS NIH HHS R01 NS027941NINDS NIH HHS R01 NS061829NINDS NIH HHS R21 NS070323PHS HHS DKO31175PHS HHS DKO31813PHS HHS NLO60056
6 · The paper itself

Abstract

Linkage disequilibrium (LD) is the non-random distribution of alleles across the genome, and it can create serious problems for modern linkage studies. In particular, computational feasibility is often obtained at the expense of power, precision, and/or accuracy. In our new approach, we combine linkage results over multiple marker subsets to provide fast, efficient, and robust analyses, without compromising power, precision, or accuracy. Allele frequencies and LD in the densely spaced markers are used to construct subsamples that are highly informative for linkage. We have tested our approach extensively, and implemented it in the software package EAGLET (Efficient Analysis of Genetic Linkage: Estimation and Testing). Relative to several commonly used methods we show that EAGLET has increased power to detect disease genes across a range of trait models, LD patterns, and family structures using both simulated and real data. In particular, when the underlying LD pattern is derived from real data, we find that EAGLET outperforms several commonly used linkage methods. In-depth analysis of family data, simulated with linkage and under the real-data derived LD pattern, showed that EAGLET had 78.1% power to detect a dominant disease with incomplete penetrance, whereas the method that uses one marker per cM had 69.7% power, and the cluster-based approach implemented in MERLIN had 76.7% power. In this same setting, EAGLET was three times faster than MERLIN, and it narrowed the MERLIN-based confidence interval for trait location by 29%. Overall, EAGLET gives researchers a fast, accurate, and powerful new tool for analyzing high-throughput linkage data, and large extended families are easily accommodated.

Indexed as

AllelesGenetic LinkageGenetic MarkersGenetic Predisposition to DiseaseSoftwareConfidence IntervalsGene FrequencyGenome, HumanHigh-Throughput Nucleotide SequencingHumansLinkage DisequilibriumPolymorphism, Single NucleotideQuantitative Trait LociSequence Analysis, DNAGenetic Markers

Identifiers

PMID21610749
PMCPMC3190261

What OpenQuestion holds

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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.