Evidence map›Paper›PMID 36046603›Full record

ArticleFrontiers in molecular biosciences2022

Predicting higher-order mutational effects in an RNA enzyme by machine learning of high-throughput experimental data.

James D Beck, Jessica M Roberts, Joey M Kitzhaber, Ashlyn Trapp, Edoardo Serra, Francesca Spezzano, Eric J Hayden

Open access · goldAbstract read
In one paragraph

Article in Frontiers in molecular biosciences, 2022. 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
0.7field-weighted citation impact, top 33% of its field
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, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. 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

7 authors at 1 institution in 1 country.

James D BeckBoise State University, Boise, ID, United States.
Jessica M RobertsBiomolecular Sciences Graduate Programs, Boise State University, Boise, ID, United States.
Joey M KitzhaberDepartment of Computer Science, Boise State University, Boise, ID, United States.
Ashlyn TrappDepartment of Biological Sciences, Boise State University, Boise, ID, United States.
Edoardo SerraBoise State University, Boise, ID, United States.
Francesca SpezzanoBoise State University, Boise, ID, United States.
Eric J HaydenBiomolecular Sciences Graduate Programs, Boise State University, Boise, ID, United States.
Boise State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ribozymes are RNA molecules that catalyze biochemical reactions. Self-cleaving ribozymes are a common naturally occurring class of ribozymes that catalyze site-specific cleavage of their own phosphodiester backbone. In addition to their natural functions, self-cleaving ribozymes have been used to engineer control of gene expression because they can be designed to alter RNA processing and stability. However, the rational design of ribozyme activity remains challenging, and many ribozyme-based systems are engineered or improved by random mutagenesis and selection (

Indexed as

epistasisfitness landscapelong short-term memorymachine learningrandom forestribozymeRNA

Identifiers

PMID36046603
PMCPMC9421044
OpenAlexW4291378374

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.