Evidence map›Paper›PMID 19829701›Full record

ArticlePloS one2009

Empirical Bayes analysis of quantitative proteomics experiments.

Adam A Margolin, Shao-En Ong, Monica Schenone, Robert Gould, Stuart L Schreiber, Steven A Carr, Todd R Golub

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

35 citing papers in PubMed, 50 citations in OpenAlex.

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  12. IonStar enables high-precision, low-missing-data proteomics quantification in large biological cohorts.Proceedings of the National Academy of Sciences of the United States of America · 2018
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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

7 authors at 3 institutions in 1 country.

Adam A MargolinCancer program, The Broad Institute of Harvard and MIT, Cambridge, Massachusetts, USA. margolin@broad.mit.edu
Shao-En Ong
Monica Schenone
Robert Gould
Stuart L Schreiber
Steven A Carr
Todd R Golub
Broad Institute · USDana-Farber Cancer Institute · USNovel (United States) · US

Funding

Discovery Pipeline (2 of 4)RL1CA133834 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI GOLUB, TODD R. · 2007 to 2011
$9.9M
Driving Medical Projects (4 of 4)RL1GM084437 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SCOLNICK, EDWARD MARK · 2007 to 2011
$5.9M
Genomics Based Drug DiscoveryUL1RR024924 · NCRR · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI SCOLNICK, EDWARD MARK · 2007 to 2007
$352k
NCI NIH HHS RL1 CA 133834NCI NIH HHS RL1 CA133834NCRR NIH HHS UL1 RR 024924NCRR NIH HHS UL1 RR024924NIGMS NIH HHS RL1 GM 084437NIGMS NIH HHS RL1 GM084437
6 · The paper itself

Abstract

backgroundAdvances in mass spectrometry-based proteomics have enabled the incorporation of proteomic data into systems approaches to biology. However, development of analytical methods has lagged behind. Here we describe an empirical Bayes framework for quantitative proteomics data analysis. The method provides a statistical description of each experiment, including the number of proteins that differ in abundance between 2 samples, the experiment's statistical power to detect them, and the false-positive probability of each protein. METHODOLOGY/PRINCIPAL

findingsWe analyzed 2 types of mass spectrometric experiments. First, we showed that the method identified the protein targets of small-molecules in affinity purification experiments with high precision. Second, we re-analyzed a mass spectrometric data set designed to identify proteins regulated by microRNAs. Our results were supported by sequence analysis of the 3' UTR regions of predicted target genes, and we found that the previously reported conclusion that a large fraction of the proteome is regulated by microRNAs was not supported by our statistical analysis of the data. CONCLUSIONS/SIGNIFICANCE: Our results highlight the importance of rigorous statistical analysis of proteomic data, and the method described here provides a statistical framework to robustly and reliably interpret such data.

Indexed as

Proteome3' Untranslated RegionsBayes TheoremComputational BiologyFalse Positive ReactionsHeLa CellsHumansMass SpectrometryModels, StatisticalNormal DistributionProteomicsReproducibility of ResultsSequence Analysis, Protein3' Untranslated RegionsProteome

Identifiers

PMID19829701
PMCPMC2759080
OpenAlexW2105898083

What OpenQuestion holds

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LicenceCC BY
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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.