Evidence map›Paper›PMID 28454776›Full record

ArticleMethods (San Diego, Calif.)2017

Functional association prediction by community profiling.

Dazhi Jiao, Wontack Han, Yuzhen Ye

Abstract read
In one paragraph

Article in Methods (San Diego, Calif.), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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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

3 authors.

Dazhi JiaoIndiana University, 150 S. Woodlawn Ave, Bloomington, IN 47405, United States.
Wontack HanIndiana University, 150 S. Woodlawn Ave, Bloomington, IN 47405, United States.
Yuzhen YeIndiana University, 150 S. Woodlawn Ave, Bloomington, IN 47405, United States. Electronic address: yye@indiana.edu.

Funding

Graph-centric approaches to metatranscriptomic and metaproteomic data analysisR01AI108888 · NIAID · TRUSTEES OF INDIANA UNIVERSITY · PI YE, YUZHEN · 2014 to 2017
$1.4M
NIAID NIH HHS R01 AI108888
6 · The paper itself

Abstract

Recent years have witnessed unprecedented accumulation of DNA sequences and therefore protein sequences (predicted from DNA sequences), due to the advances of sequencing technology. One of the major sources of the hypothetical proteins is the metagenomics research. Current annotation of metagenomes (collections of short metagenomic sequences or assemblies) relies on similarity searches against known gene/protein families, based on which functional profiles of microbial communities can be built. This practice, however, leaves out the hypothetical proteins, which may outnumber the known proteins for many microbial communities. On the other hand, we may ask: what can we gain from the large number of metagenomes made available by the metagenomic studies, for the annotation of metagenomic sequences as well as functional annotation of hypothetical proteins in general? Here we propose a community profiling approach for predicting functional associations between proteins: two proteins are predicted to be associated if they share similar presence and absence profiles (called community profiles) across microbial communities. Community profiling is conceptually similar to the phylogenetic profiling approach to functional prediction, however with fundamental differences. We tested different profile construction methods, the selection of reference metagenomes, and correlation metrics, among others, to optimize the performance of this new approach. We demonstrated that the community profiling approach alone slightly outperforms the phylogenetic profiling approach for associating proteins in species that are well represented by sequenced genomes, and combining phylogenetic and community profiling further improves (though only marginally) the prediction of functional association. Further we showed that community profiling method significantly outperforms phylogenetic profiling, revealing more functional associations, when applied to a more recently sequenced bacterial genome.

Indexed as

MetagenomicsSoftwareAlgorithmsComputational BiologyDatabases, GeneticGenome, BacterialMicrobial ConsortiaPhylogenySequence Analysis, DNACommunity profilingFunctional association predictionGuilt-by-associationMetagenomicsPhylogenetic profiling

Identifiers

PMID28454776
PMCPMC5643221

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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.