Evidence map›Paper›PMID 15469612›Full record

ArticleBMC bioinformatics2004

Overdispersed logistic regression for SAGE: modelling multiple groups and covariates.

Keith A Baggerly, Li Deng, Jeffrey S Morris, C Marcelo Aldaz

Abstract readComparative Study
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 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

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  8. A Bayesian Semi-parametric Approach for the Differential Analysis of Sequence Counts Data.Journal of the Royal Statistical Society. Series C, Applied statistics · 2014
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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

4 authors.

Keith A BaggerlyDepartment of Biostatistics and Applied Mathematics, UT M. D. Anderson Cancer Center, Houston, TX, USA. kabagg@mdanderson.org
Li Deng
Jeffrey S Morris
C Marcelo Aldaz

Funding

High resolution transcriptome analysis: lnn breast cancerU19CA084978 · NCI · UNIVERSITY OF TEXAS MD ANDERSON CAN CTR · PI ALDAZ, C. MARCELO · 2001 to 2004
$4.8M
NCI NIH HHS 1U19 CA84978-1A1NCI NIH HHS U19 CA084978
6 · The paper itself

Abstract

backgroundTwo major identifiable sources of variation in data derived from the Serial Analysis of Gene Expression (SAGE) are within-library sampling variability and between-library heterogeneity within a group. Most published methods for identifying differential expression focus on just the sampling variability. In recent work, the problem of assessing differential expression between two groups of SAGE libraries has been addressed by introducing a beta-binomial hierarchical model that explicitly deals with both of the above sources of variation. This model leads to a test statistic analogous to a weighted two-sample t-test. When the number of groups involved is more than two, however, a more general approach is needed.

resultsWe describe how logistic regression with overdispersion supplies this generalization, carrying with it the framework for incorporating other covariates into the model as a byproduct. This approach has the advantage that logistic regression routines are available in several common statistical packages.

conclusionsThe described method provides an easily implemented tool for analyzing SAGE data that correctly handles multiple types of variation and allows for more flexible modelling.

Indexed as

Analysis of VarianceCell Line, TumorColonColonic NeoplasmsDNADNA, NeoplasmGene Expression ProfilingGene Expression RegulationGene LibraryHumansLogistic ModelsMathematical ComputingMultivariate AnalysisRectal NeoplasmsDNADNA, Neoplasm

Identifiers

PMID15469612
PMCPMC524524

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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.