Evidence map›Paper›PMID 33313544›Full record

ArticlePlant phenomics (Washington, D.C.)2020

Computing on Phenotypic Descriptions for Candidate Gene Discovery and Crop Improvement.

Ian R Braun, Colleen F Yanarella, Carolyn J Lawrence-Dill

Abstract read
In one paragraph

Article in Plant phenomics (Washington, D.C.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

3 authors.

Ian R Braun *Interdepartmental Bioinformatics and Computational Biology, Iowa State University, Ames, IA 50011, USA.
Colleen F Yanarella *Interdepartmental Bioinformatics and Computational Biology, Iowa State University, Ames, IA 50011, USA.
Carolyn J Lawrence-DillInterdepartmental Bioinformatics and Computational Biology, Iowa State University, Ames, IA 50011, USA.ORCID https://orcid.org/0000-0003-0069-1430

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Many newly observed phenotypes are first described, then experimentally manipulated. These language-based descriptions appear in both the literature and in community datastores. To standardize phenotypic descriptions and enable simple data aggregation and analysis, controlled vocabularies and specific data architectures have been developed. Such simplified descriptions have several advantages over natural language: they can be rigorously defined for a particular context or problem, they can be assigned and interpreted programmatically, and they can be organized in a way that allows for semantic reasoning (inference of implicit facts). Because researchers generally report phenotypes in the literature using natural language, curators have been translating phenotypic descriptions into controlled vocabularies for decades to make the information computable. Unfortunately, this methodology is highly dependent on human curation, which does not scale to the scope of all publications available across all of plant biology. Simultaneously, researchers in other domains have been working to enable computation on natural language. This has resulted in new, automated methods for computing on language that are now available, with early analyses showing great promise. Natural language processing (NLP) coupled with machine learning (ML) allows for the use of unstructured language for direct analysis of phenotypic descriptions. Indeed, we have found that these automated methods can be used to create data structures that perform as well or better than those generated by human curators on tasks such as predicting gene function and biochemical pathway membership. Here, we describe current and ongoing efforts to provide tools for the plant phenomics community to explore novel predictions that can be generated using these techniques. We also describe how these methods could be used along with mobile speech-to-text tools to collect and analyze in-field spoken phenotypic descriptions for association genetics and breeding applications.

Identifiers

PMID33313544
PMCPMC7706311

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LicenceCC BY
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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.