Evidence map›Paper›PMID 38523792›Full record

ArticleiScience2024

KinPred-RNA-kinase activity inference and cancer type classification using machine learning on RNA-seq data.

Yuntian Zhang, Lantian Yao, Chia-Ru Chung, Yixian Huang, Shangfu Li, Wenyang Zhang, Yuxuan Pang, Tzong-Yi Lee

Open access · goldAbstract read
In one paragraph

Article in iScience, 2024. 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
0.7field-weighted citation impact, top 32% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  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

8 authors at 4 institutions in 3 countries.

Yuntian ZhangWarshel Institute for Computational Biology, The Chinese University of Hong Kong, Shenzhen 518172, China.
Lantian YaoSchool of Science and Engineering, The Chinese University of Hong Kong, Shenzhen 518172, China.
Chia-Ru ChungDepartment of Computer Science and Information Engineering, National Central University, Taoyuan 320953, Taiwan.
Yixian HuangWarshel Institute for Computational Biology, The Chinese University of Hong Kong, Shenzhen 518172, China.
Shangfu LiWarshel Institute for Computational Biology, The Chinese University of Hong Kong, Shenzhen 518172, China.
Wenyang ZhangSchool of Medicine, The Chinese University of Hong Kong, Shenzhen 518172, China.
Yuxuan PangDivision of Health Medical Intelligence, Human Genome Center, The Institute of Medical Science, The University of Tokyo, Minato-ku, Tokyo, Japan.
Tzong-Yi LeeInstitute of Bioinformatics and Systems Biology, National Yang Ming Chiao Tung University, Hsinchu 300093, Taiwan.
Chinese University of Hong Kong, Shenzhen · CNNational Central University · TWNational Yang Ming Chiao Tung University · TWThe University of Tokyo · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kinases as important enzymes can transfer phosphate groups from high-energy and phosphate-donating molecules to specific substrates and play essential roles in various cellular processes. Existing algorithms for kinase activity from phosphorylated proteomics data are often costly, requiring valuable samples. Moreover, methods to extract kinase activities from bulk RNA sequencing data remain undeveloped. In this study, we propose a computational framework KinPred-RNA to derive kinase activities from bulk RNA-sequencing data in cancer samples. KinPred-RNA framework, using the extreme gradient boosting (XGBoost) regression model, outperforms random forest regression, multiple linear regression, and support vector machine regression models in predicting kinase activities from cancer-related RNA sequencing data. Efficient gene signatures from the LINCS-L1000 dataset were used as inputs for KinPred-RNA. The results highlight its potential to be related to biological function. In conclusion, KinPred RNA constitutes a significant advance in cancer research by potentially facilitating the identification of cancer.

Indexed as

CancerMachine learning

Identifiers

PMID38523792
PMCPMC10959666
OpenAlexW4392231372

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.