Evidence map›Paper›PMID 30029596›Full record

ArticleBMC genomics2018

RNA-seq assistant: machine learning based methods to identify more transcriptional regulated genes.

Likai Wang, Yanpeng Xi, Sibum Sung, Hong Qiao

Open access · goldAbstract readValidation Study
In one paragraph

Article in BMC genomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

29 citing papers in PubMed, 66 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Likai WangInstitute for Cellular and Molecular Biology, The University of Texas at Austin, 2506 Speedway, NMS 5.324, Austin, TX, 78712, USA.
Yanpeng XiInstitute for Cellular and Molecular Biology, The University of Texas at Austin, 2506 Speedway, NMS 5.324, Austin, TX, 78712, USA.
Sibum SungInstitute for Cellular and Molecular Biology, The University of Texas at Austin, 2506 Speedway, NMS 5.324, Austin, TX, 78712, USA.
Hong QiaoInstitute for Cellular and Molecular Biology, The University of Texas at Austin, 2506 Speedway, NMS 5.324, Austin, TX, 78712, USA. hqiao@austin.utexas.edu.
The University of Texas at Austin · US

Funding

Coordinated regulation of floral transition by protein and long noncoding RNA componentsR01GM100108 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI SUNG, SIBUM · 2012 to 2025
$4.0M
Molecular mechanisms of interplay between ethylene signaling and chromatin regulation in ArabidopsisR01GM115879 · NIGMS · UNIVERSITY OF TEXAS AT AUSTIN · PI QIAO, HONG · 2015 to 2023
$2.9M
National Institutes of Health NIH-1R01GM115879-01National Institutes of Health NIH-2R01GM100108National Science Foundation NSF IOS 1656764NIGMS NIH HHS R01 GM100108NIGMS NIH HHS R01 GM115879
6 · The paper itself

Abstract

backgroundAlthough different quality controls have been applied at different stages of the sample preparation and data analysis to ensure both reproducibility and reliability of RNA-seq results, there are still limitations and bias on the detectability for certain differentially expressed genes (DEGs). Whether the transcriptional dynamics of a gene can be captured accurately depends on experimental design/operation and the following data analysis processes. The workflow of subsequent data processing, such as reads alignment, transcript quantification, normalization, and statistical methods for ultimate identification of DEGs can influence the accuracy and sensitivity of DEGs analysis, producing a certain number of false-positivity or false-negativity. Machine learning (ML) is a multidisciplinary field that employs computer science, artificial intelligence, computational statistics and information theory to construct algorithms that can learn from existing data sets and to make predictions on new data set. ML-based differential network analysis has been applied to predict stress-responsive genes through learning the patterns of 32 expression characteristics of known stress-related genes. In addition, the epigenetic regulation plays critical roles in gene expression, therefore, DNA and histone methylation data has been shown to be powerful for ML-based model for prediction of gene expression in many systems, including lung cancer cells. Therefore, it is promising that ML-based methods could help to identify the DEGs that are not identified by traditional RNA-seq method.

resultsWe identified the top 23 most informative features through assessing the performance of three different feature selection algorithms combined with five different classification methods on training and testing data sets. By comprehensive comparison, we found that the model based on InfoGain feature selection and Logistic Regression classification is powerful for DEGs prediction. Moreover, the power and performance of ML-based prediction was validated by the prediction on ethylene regulated gene expression and the following qRT-PCR.

conclusionsOur study shows that the combination of ML-based method with RNA-seq greatly improves the sensitivity of DEGs identification.

Indexed as

Epigenesis, GeneticMachine LearningArabidopsisGene Expression ProfilingHistone CodeHumansSequence Analysis, RNATranscription, GeneticArabidopsisDifferentially expressed genes (DEGs)EthyleneMachine learning

Identifiers

PMID30029596
PMCPMC6053725
OpenAlexW2884418830

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.