Evidence map›Paper›PMID 26811807›Full record

ArticleCurrent plant biology2015

Dual use of peptide mass spectra: Protein atlas and genome annotation.

Justin W Walley, Steven P Briggs

Abstract read
In one paragraph

Article in Current plant biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
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  4. Article
  5. Article
  6. Review
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.

Justin W WalleyUniversity of California San Diego, Section of Cell & Developmental Biology, La Jolla, CA 92093-0380, United States.
Steven P BriggsUniversity of California San Diego, Section of Cell & Developmental Biology, La Jolla, CA 92093-0380, United States.

Funding

Mechanisms by which a fungal HDAC inhibitor suppresses innate immunity in maizeF32GM096707 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI WALLEY, JUSTIN WILLIAM · 2011 to 2012
$101k
NIGMS NIH HHS F32 GM096707
6 · The paper itself

Abstract

One of the objectives of genome science is the discovery and accurate annotation of all protein-coding genes. Proteogenomics has emerged as a methodology that provides orthogonal information to traditional forms of evidence used for genome annotation. By this method, peptides that are identified via tandem mass spectrometry are used to refine protein-coding gene models. Namely, these peptides are used to confirm the translation of predicted protein-coding genes, as evidence of novel genes or for correction of current gene models. Proteogenomics requires deep and broad sampling of the proteome in order to generate sufficient numbers of unique peptides. Therefore, we propose that proteogenomic projects are designed so that the generated peptides can also be used to create a comprehensive protein atlas that quantitatively catalogues protein abundance changes during development and in response to environmental stimulus.

Indexed as

AnnotationAtlasProteogenomicsProteomics

Identifiers

PMID26811807
PMCPMC4723421

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.