Evidence map›Paper›PMID 36959975›Full record

ReviewFrontiers in bioinformatics2023

Exploring microbial functional biodiversity at the protein family level-From metagenomic sequence reads to annotated protein clusters.

Fotis A Baltoumas, Evangelos Karatzas, David Paez-Espino, Nefeli K Venetsianou, Eleni Aplakidou, Anastasis Oulas, Robert D Finn, Sergey Ovchinnikov, Evangelos Pafilis, Nikos C Kyrpides and 1 more

Full text readReview
In one paragraph

Review in Frontiers in bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Visualizing metagenomic and metatranscriptomic data: A comprehensive review.Computational and structural biotechnology journal · 2024
    Review
  8. 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

11 authors.

Fotis A BaltoumasInstitute for Fundamental Biomedical Research, BSRC "Alexander Fleming", Vari, Greece.
Evangelos KaratzasInstitute for Fundamental Biomedical Research, BSRC "Alexander Fleming", Vari, Greece.
David Paez-EspinoLawrence Berkeley National Laboratory, DOE Joint Genome Institute, Berkeley, CA, United States.
Nefeli K VenetsianouInstitute for Fundamental Biomedical Research, BSRC "Alexander Fleming", Vari, Greece.
Eleni AplakidouInstitute for Fundamental Biomedical Research, BSRC "Alexander Fleming", Vari, Greece.
Anastasis OulasThe Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.
Robert D FinnEuropean Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Genome Campus, Cambridge, United Kingdom.
Sergey OvchinnikovJohn Harvard Distinguished Science Fellowship Program, Harvard University, Cambridge, MA, United States.
Evangelos PafilisInstitute of Marine Biology, Biotechnology and Aquaculture (IMBBC), Hellenic Centre for Marine Research (HCMR), Heraklion, Greece.
Nikos C KyrpidesLawrence Berkeley National Laboratory, DOE Joint Genome Institute, Berkeley, CA, United States.
Georgios A PavlopoulosInstitute for Fundamental Biomedical Research, BSRC "Alexander Fleming", Vari, Greece.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metagenomics has enabled accessing the genetic repertoire of natural microbial communities. Metagenome shotgun sequencing has become the method of choice for studying and classifying microorganisms from various environments. To this end, several methods have been developed to process and analyze the sequence data from raw reads to end-products such as predicted protein sequences or families. In this article, we provide a thorough review to simplify such processes and discuss the alternative methodologies that can be followed in order to explore biodiversity at the protein family level. We provide details for analysis tools and we comment on their scalability as well as their advantages and disadvantages. Finally, we report the available data repositories and recommend various approaches for protein family annotation related to phylogenetic distribution, structure prediction and metadata enrichment.

Indexed as

biodiversitycluster annotationmetagenomesmetatranscriptomesmicrobial dark matterprotein clusteringprotein families

Identifiers

PMID36959975
PMCPMC10029925

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measurements read36
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.