Evidence map›Paper›PMID 34976025›Full record

ArticleFrontiers in genetics2021

Using Machine Learning Approaches to Predict Target Gene Expression in Rice T-DNA Insertional Mutants.

Ching-Hsuan Chien, Lan-Ying Huang, Shuen-Fang Lo, Liang-Jwu Chen, Chi-Chou Liao, Jia-Jyun Chen, Yen-Wei Chu

Abstract read
In one paragraph

Article in Frontiers in genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

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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 synthesis or guideline pooled it.

  1. Pooled it
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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.

Ching-Hsuan ChienPh.D. Program in Medical Biotechnology, National Chung Hsing University, Taichung, Taiwan.
Lan-Ying HuangPh.D. Program in Medical Biotechnology, National Chung Hsing University, Taichung, Taiwan.
Shuen-Fang LoBiotechnology Center, National Chung Hsing University, Taichung, Taiwan.
Liang-Jwu ChenInstitute of Molecular Biology, National Chung Hsing University, Taichung, Taiwan.
Chi-Chou LiaoInstitute of Molecular Biology, National Chung Hsing University, Taichung, Taiwan.
Jia-Jyun ChenInstitute of Genomics and Bioinformatics, National Chung Hsing University, Taichung, Taiwan.
Yen-Wei ChuPh.D. Program in Medical Biotechnology, National Chung Hsing University, Taichung, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To change the expression of the flanking genes by inserting T-DNA into the genome is commonly used in rice functional gene research. However, whether the expression of a gene of interest is enhanced must be validated experimentally. Consequently, to improve the efficiency of screening activated genes, we established a model to predict gene expression in T-DNA mutants through machine learning methods. We gathered experimental datasets consisting of gene expression data in T-DNA mutants and captured the PROMOTER and MIDDLE sequences for encoding. In first-layer models, support vector machine (SVM) models were constructed with nine features consisting of information about biological function and local and global sequences. Feature encoding based on the PROMOTER sequence was weighted by logistic regression. The second-layer models integrated 16 first-layer models with minimum redundancy maximum relevance (mRMR) feature selection and the LADTree algorithm, which were selected from nine feature selection methods and 65 classified methods, respectively. The accuracy of the final two-layer machine learning model, referred to as TIMgo, was 99.3% based on fivefold cross-validation, and 85.6% based on independent testing. We discovered that the information within the local sequence had a greater contribution than the global sequence with respect to classification. TIMgo had a good predictive ability for target genes within 20 kb from the 35S enhancer. Based on the analysis of significant sequences, the G-box regulatory sequence may also play an important role in the activation mechanism of the 35S enhancer.

Indexed as

CaMV 35S enhancergene expressionmachine learningriceT-DNA activation tagging

Identifiers

PMID34976025
PMCPMC8718795

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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.