Evidence map›Paper›PMID 18613952›Full record

ArticleGenome biology2008

An en masse phenotype and function prediction system for Mus musculus.

Murat Taşan, Weidong Tian, David P Hill, Francis D Gibbons, Judith A Blake, Frederick P Roth

Abstract read
In one paragraph

Article in Genome biology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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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

6 authors.

Murat TaşanDepartment of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Longwood Avenue, Boston, Massachusetts 02115, USA.
Weidong Tian
David P Hill
Francis D Gibbons
Judith A Blake
Frederick P Roth

Funding

Resource ProjectU41HG002273 · NHGRI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI THOMAS, PAUL D. · 2012 to 2021
$34.7M
Genomic Analysis of Network Perturbations in Human DiseaseP50HG004233 · NHGRI · DANA-FARBER CANCER INST · PI VIDAL, MARC · 2007 to 2017
$31.6M
Gene Ontology ConsortiumP41HG002273 · NHGRI · JACKSON LABORATORY · PI BLAKE, JUDITH A · 2004 to 2011
$27.4M
GENE ONTOLOGY CONSORTIUMR01HG002273 · NHGRI · JACKSON LABORATORY · PI BLAKE, JUDITH A · 2001 to 2003
$5.8M
Computational Methods for Directed Functional GenomicsR01HG003224 · NHGRI · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI ROTH, FREDERICK P · 2005 to 2010
$2.2M
Interdisciplinary Training in Genetics & Complex DiseaseR90DK071507 · NIDDK · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI WESSLING-RESNICK, MARIANNE · 2004 to 2008
$1.1M
Biological prediction by integrated probabilistic modelsF32HG004098 · NHGRI · HARVARD MEDICAL SCHOOL · PI TASAN, MURAT · 2006 to 2008
$90k
NHGRI NIH HHS F32 HG004098NHGRI NIH HHS F32HG004098NHGRI NIH HHS HG0017115NHGRI NIH HHS HG002273NHGRI NIH HHS HG003224NHGRI NIH HHS P41 HG002273NHGRI NIH HHS P50 HG004233NHGRI NIH HHS R01 HG002273NHGRI NIH HHS R01 HG003224NHGRI NIH HHS U41 HG002273NIDDK NIH HHS DK071507NIDDK NIH HHS R90 DK071507
6 · The paper itself

Abstract

backgroundIndividual researchers are struggling to keep up with the accelerating emergence of high-throughput biological data, and to extract information that relates to their specific questions. Integration of accumulated evidence should permit researchers to form fewer - and more accurate - hypotheses for further study through experimentation.

resultsHere a method previously used to predict Gene Ontology (GO) terms for Saccharomyces cerevisiae (Tian et al.: Combining guilt-by-association and guilt-by-profiling to predict Saccharomyces cerevisiae gene function. Genome Biol 2008, 9(Suppl 1):S7) is applied to predict GO terms and phenotypes for 21,603 Mus musculus genes, using a diverse collection of integrated data sources (including expression, interaction, and sequence-based data). This combined 'guilt-by-profiling' and 'guilt-by-association' approach optimizes the combination of two inference methodologies. Predictions at all levels of confidence are evaluated by examining genes not used in training, and top predictions are examined manually using available literature and knowledge base resources.

conclusionWe assigned a confidence score to each gene/term combination. The results provided high prediction performance, with nearly every GO term achieving greater than 40% precision at 1% recall. Among the 36 novel predictions for GO terms and 40 for phenotypes that were studied manually, >80% and >40%, respectively, were identified as accurate. We also illustrate that a combination of 'guilt-by-profiling' and 'guilt-by-association' outperforms either approach alone in their application to M. musculus.

Indexed as

AlgorithmsAnimalsArtificial IntelligenceMetabolic Networks and PathwaysMiceProteinsTerminology as TopicProteins

Identifiers

PMID18613952
PMCPMC2447542

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.