Evidence map›Paper›PMID 36828128›Full record

ReviewMolecular & cellular proteomics : MCP2023

Challenges and Opportunities for Single-cell Computational Proteomics.

Hannah Boekweg, Samuel H Payne

Abstract readReview
In one paragraph

Review in Molecular & cellular proteomics : MCP, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Review
  8. Mass Spectrometry-based Solutions for Single-cell Proteomics.Genomics, proteomics & bioinformatics · 2025
    Review
  9. Review
  10. Attracting Computational Researchers to Proteomics.Journal of the American Society for Mass Spectrometry · 2024
    Article
  11. Review
  12. Article
  13. 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

2 authors.

Hannah BoekwegBiology Department, Brigham Young University, Provo, Utah, USA.
Samuel H PayneBiology Department, Brigham Young University, Provo, Utah, USA. Electronic address: sam_payne@byu.edu.

Funding

Enhanced Sensitivity and Quantitative Precision for Single Cell ProteomicsR01GM147653 · NIGMS · BRIGHAM YOUNG UNIVERSITY · PI PAYNE, SAMUEL H, SHORTREED, MICHAEL R · 2022 to 2025
$1.6M
NIGMS NIH HHS R01 GM147653
6 · The paper itself

Abstract

Single-cell proteomics is growing rapidly and has made several technological advancements. As most research has been focused on improving instrumentation and sample preparation methods, very little attention has been given to algorithms responsible for identifying and quantifying proteins. Given the inherent difference between bulk data and single-cell data, it is necessary to realize that current algorithms being employed on single-cell data were designed for bulk data and have underlying assumptions that may not hold true for single-cell data. In order to develop and optimize algorithms for single-cell data, we need to characterize the differences between single-cell data and bulk data and assess how current algorithms perform on single-cell data. Here, we present a review of algorithms responsible for identifying and quantifying peptides and proteins. We will give a review of how each type of algorithm works, assumptions it relies on, how it performs on single-cell data, and possible optimizations and solutions that could be used to address the differences in single-cell data.

Indexed as

ProteinsProteomicsAlgorithmsPeptidesPeptidesProteinsalgorithmbioinformaticspeptide identificationquantificationsingle-cell proteomics

Identifiers

PMID36828128
PMCPMC10060113

What OpenQuestion holds

Textmetadata
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.