Evidence map›Paper›PMID 36910011›Full record

ArticleProceedings. IEEE International Conference on Bioinformatics and Biomedicine2022

FineFDR: Fine-grained Taxonomy-specific False Discovery Rates Control in Metaproteomics.

Shengze Wang, Shichao Feng, Chongle Pan, Xuan Guo

Abstract read
In one paragraph

Article in Proceedings. IEEE International Conference on Bioinformatics and Biomedicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Nanopore sequencing enables novel detection of deuterium incorporation in DNA.Computational and structural biotechnology journal · 2024
    Article
  2. SEMQuant: Extending Sipros-Ensemble with Match-Between-Runs for Comprehensive Quantitative Metaproteomics.Bioinformatics research and applications : ... international symposium, ISBRA ... proceedings. ISBRA (Conference) · 2024
    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.

Shengze WangDepartment of Computer Science and Engineering University of North Texas, Denton, TX 76207, United States.
Shichao FengDepartment of Computer Science and Engineering University of North Texas, Denton, TX 76207, United States.
Chongle PanSchool of Computer Science Department of Microbiology and Plant Biology, University of Oklahoma, Norman, OK 73019, United States.
Xuan GuoDepartment of Computer Science and Engineering University of North Texas, Denton, TX 76207, United States.

Funding

Proteomic Stable Isotope Probing as a Novel Approach for Linking Prebiotics with Active Gut MicrobiotaR01AT011618 · NCCIH · UNIVERSITY OF OKLAHOMA · PI PAN, CHONGLE · 2021 to 2025
$1.8M
A Computational Framework for Protein Identification and Quantification in Metaproteomics Using Data-Independent AcquisitionR15LM013460 · NLM · UNIVERSITY OF NORTH TEXAS · PI GUO, XUAN · 2020 to 2020
$361k
NCCIH NIH HHS R01 AT011618NLM NIH HHS R15 LM013460
6 · The paper itself

Abstract

Microbial community proteomics, also termed metaproteomics, investigates all proteins expressed by a microbiota. Tandem mass spectrometry (MS/MS) is the typical method for identifying proteins in metaproteomics, which involves searching the mass spectra against a protein sequence database. A major post-analysis step is controlling the false discovery rate (FDR), i.e., the ratio of false positives to the total number of annotations. The current popular target-decoy FDR estimation method treats all the peptides and proteins equally and overlooks that they could have varied probabilities of being identified. In this study, we report FineFDR, a framework for FDR assessment at fine-grained levels with taxonomy information considered. FineFDR groups the identified peptide-spectrum matches, peptides, and proteins from different taxonomic units and estimates the FDR in each group separately. Empirical experiments on the simulated and real-world data sets demonstrate that our FineFDR achieved higher precision and more peptide and protein identifications when compared to the state-of-the-art methods, such as Comet, Percolator, TIDD, and Tailor. FineFDR is freely available under the GNU GPL license at https://github.com/Biocomputing-Research-Group/FDR.

Indexed as

MetaproteomicsTarget-decoy SearchTaxonomy-specific FDR Control

Identifiers

PMID36910011
PMCPMC9998077

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.