Evidence map›Paper›PMID 27400380›Full record

ArticlePLoS computational biology2016

Metagenome and Metatranscriptome Analyses Using Protein Family Profiles.

Cuncong Zhong, Anna Edlund, Youngik Yang, Jeffrey S McLean, Shibu Yooseph

Abstract read
In one paragraph

Article in PLoS computational biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. IntegratedNAR genomics and bioinformatics · 2023
    Article
  7. Article
  8. Article
  9. Review
  10. 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

5 authors.

Cuncong ZhongJ. Craig Venter Institute, La Jolla, California, United States of America.
Anna EdlundJ. Craig Venter Institute, La Jolla, California, United States of America.
Youngik YangJ. Craig Venter Institute, La Jolla, California, United States of America.
Jeffrey S McLeanJ. Craig Venter Institute, La Jolla, California, United States of America.ORCID 0000-0001-9934-5137
Shibu YoosephJ. Craig Venter Institute, La Jolla, California, United States of America.

Funding

Making a quantum leap in plaque research with modern sciencesR01DE020102 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI HE, XUESONG, MCLEAN, JEFFREY SCOTT · 2010 to 2020
$3.7M
Moving Beyond Diversity by Revealing Biological Functions of Uncultured BacteriaR01GM095373 · NIGMS · J. CRAIG VENTER INSTITUTE, INC. · PI MCLEAN, JEFFREY SCOTT, YOOSEPH, SHIBU · 2011 to 2014
$1.7M
Investigating Oral Pathogen Virulence within Complex Oral Biofilm CommunitiesR00DE024543 · NIDCR · J. CRAIG VENTER INSTITUTE, INC. · PI EDLUND, ANNA ELISABET · 2016 to 2018
$732k
Investigating oral pathogen virulence within complex oral biofilm communitiesK99DE024543 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI EDLUND, ANNA ELISABET · 2014 to 2015
$188k
NIDCR NIH HHS K99 DE024543NIDCR NIH HHS R01 DE020102NIGMS NIH HHS R01 GM095373
6 · The paper itself

Abstract

Analyses of metagenome data (MG) and metatranscriptome data (MT) are often challenged by a paucity of complete reference genome sequences and the uneven/low sequencing depth of the constituent organisms in the microbial community, which respectively limit the power of reference-based alignment and de novo sequence assembly. These limitations make accurate protein family classification and abundance estimation challenging, which in turn hamper downstream analyses such as abundance profiling of metabolic pathways, identification of differentially encoded/expressed genes, and de novo reconstruction of complete gene and protein sequences from the protein family of interest. The profile hidden Markov model (HMM) framework enables the construction of very useful probabilistic models for protein families that allow for accurate modeling of position specific matches, insertions, and deletions. We present a novel homology detection algorithm that integrates banded Viterbi algorithm for profile HMM parsing with an iterative simultaneous alignment and assembly computational framework. The algorithm searches a given profile HMM of a protein family against a database of fragmentary MG/MT sequencing data and simultaneously assembles complete or near-complete gene and protein sequences of the protein family. The resulting program, HMM-GRASPx, demonstrates superior performance in aligning and assembling homologs when benchmarked on both simulated marine MG and real human saliva MG datasets. On real supragingival plaque and stool MG datasets that were generated from healthy individuals, HMM-GRASPx accurately estimates the abundances of the antimicrobial resistance (AMR) gene families and enables accurate characterization of the resistome profiles of these microbial communities. For real human oral microbiome MT datasets, using the HMM-GRASPx estimated transcript abundances significantly improves detection of differentially expressed (DE) genes. Finally, HMM-GRASPx was used to reconstruct comprehensive sets of complete or near-complete protein and nucleotide sequences for the query protein families. HMM-GRASPx is freely available online from http://sourceforge.net/projects/hmm-graspx.

Indexed as

AlgorithmsAnti-Bacterial AgentsBacteriaComputational BiologyComputer SimulationDatabases, GeneticDrug Resistance, BacterialGene Expression ProfilingHumansMetagenomeMetagenomicsModels, TheoreticalProteinsSalivaTranscriptomeAnti-Bacterial AgentsProteins

Identifiers

PMID27400380
PMCPMC4939949

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.