Evidence map›Paper›PMID 25198674›Full record

ArticlePloS one2014

Statistical approach of functional profiling for a microbial community.

Lingling An, Nauromal Pookhao, Hongmei Jiang, Jiannong Xu

Abstract read
In one paragraph

Article in PloS one, 2014. 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
  2. Article
  3. Article
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.

Lingling AnDepartment of Agricultural & Biosystems Engineering, University of Arizona, Tucson, Arizona, United States of America; Interdisciplinary Programs in Statistics, University of Arizona, Tucson, Arizona, United States of America.
Nauromal PookhaoDepartment of Agricultural & Biosystems Engineering, University of Arizona, Tucson, Arizona, United States of America.
Hongmei JiangDepartment of Statistics, Northwestern University, Evanston, Illinois, United States of America.
Jiannong XuDepartment of Biology, New Mexico State University, Las Cruces, New Mexico, United States of America.

Funding

SOUTHWEST ENVIRONMENTAL HEALTH SCIENCES CENTERP30ES006694 · NIEHS · UNIVERSITY OF ARIZONA · PI DEAN BILLHEIMER · 1994 to 2026
$36.7M
Mosquito larval immunity and its impact on gut microbiota and malaria competenceSC2GM092789 · NIGMS · NEW MEXICO STATE UNIVERSITY LAS CRUCES · PI XU, JIANNONG · 2011 to 2013
$417k
NIEHS NIH HHS P30 ES006694NIGMS NIH HHS SC2 GM092789
6 · The paper itself

Abstract

backgroundMetagenomics is a relatively new but fast growing field within environmental biology and medical sciences. It enables researchers to understand the diversity of microbes, their functions, cooperation, and evolution in a particular ecosystem. Traditional methods in genomics and microbiology are not efficient in capturing the structure of the microbial community in an environment. Nowadays, high-throughput next-generation sequencing technologies are powerfully driving the metagenomic studies. However, there is an urgent need to develop efficient statistical methods and computational algorithms to rapidly analyze the massive metagenomic short sequencing data and to accurately detect the features/functions present in the microbial community. Although several issues about functions of metagenomes at pathways or subsystems level have been investigated, there is a lack of studies focusing on functional analysis at a low level of a hierarchical functional tree, such as SEED subsystem tree.

resultsA two-step statistical procedure (metaFunction) is proposed to detect all possible functional roles at the low level from a metagenomic sample/community. In the first step a statistical mixture model is proposed at the base of gene codons to estimate the abundances for the candidate functional roles, with sequencing error being considered. As a gene could be involved in multiple biological processes the functional assignment is therefore adjusted by utilizing an error distribution in the second step. The performance of the proposed procedure is evaluated through comprehensive simulation studies. Compared with other existing methods in metagenomic functional analysis the new approach is more accurate in assigning reads to functional roles, and therefore at more general levels. The method is also employed to analyze two real data sets.

conclusionsmetaFunction is a powerful tool in accurate profiling functions in a metagenomic sample.

Indexed as

MetagenomicsHumans

Identifiers

PMID25198674
PMCPMC4157783

What OpenQuestion holds

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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.