Evidence map›Paper›PMID 15563371›Full record

ArticleBMC bioinformatics2004

A new mixture model approach to analyzing allelic-loss data using Bayes factors.

Manisha Desai, Mary J Emond

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2004. 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
0.4field-weighted citation impact, top 34% of its field
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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Identification of pharmacogenetic markers in smoking cessation therapy.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2008
    Trial
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 at 2 institutions in 1 country.

Manisha DesaiDepartment of Biostatistics, Columbia University, 722 West 168th Street, R629, New York, NY 10032, USA. manisha.desai@columbia.edu
Mary J Emond
Columbia University · USUniversity of Washington · US

Funding

Developing Data-Driven Cancer ResearchersT32CA009168 · NCI · UNIVERSITY OF WASHINGTON · PI STEPHEN M SCHWARTZ, MICHAEL Chiao-An WU · 1985 to 2026
$10.1M
STATISTICAL ANALYSIS OF GENETIC EVENTS IN TUMORIGENESISR29CA077607 · NCI · UNIVERSITY OF WASHINGTON · PI EMOND, MARY J · 1998 to 2003
$309k
NCI NIH HHS 5R29CA77607NCI NIH HHS 5T32CA0916825NCI NIH HHS R29 CA077607
6 · The paper itself

Abstract

backgroundAllelic-loss studies record data on the loss of genetic material in tumor tissue relative to normal tissue at various loci along the genome. As the deletion of a tumor suppressor gene can lead to tumor development, one objective of these studies is to determine which, if any, chromosome arms harbor tumor suppressor genes.

resultsWe propose a large class of mixture models for describing the data, and we suggest using Bayes factors to select a reasonable model from the class in order to classify the chromosome arms. Bayes factors are especially useful in the case of testing that the number of components in a mixture model is n0 versus n1. In these cases, frequentist test statistics based on the likelihood ratio statistic have unknown distributions and are therefore not applicable. Our simulation study shows that Bayes factors favor the right model most of the time when tumor suppressor genes are present. When no tumor suppressor genes are present and background allelic-loss varies, the Bayes factors are often inconclusive, although this results in a markedly reduced false-positive rate compared to that of standard frequentist approaches. Application of our methods to three data sets of esophageal adenocarcinomas yields interesting differences from those results previously published.

conclusionsOur results indicate that Bayes factors are useful for analyzing allelic-loss data.

Indexed as

Bayes TheoremModels, GeneticAdenocarcinomaChromosomes, HumanDatabases, GeneticEsophageal NeoplasmsGenes, NeoplasmGenes, Tumor SuppressorHumansLoss of Heterozygosity

Identifiers

PMID15563371
PMCPMC544187
OpenAlexW2105446147

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.