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Jincai Feng

dblp:362/2348 · DBLP profile ↗
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2ranked-venue papers
0as first author
2since 2021 · last 2023
0000-0002-9724-0398ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Human-computer interaction and ubiquitous computing · 1 · 1 since 2021Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 62% Medical and health informatics · 38%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Medical and health informatics
clinical decision support
0.712023
diseaseGPS: auxiliary diagnostic system for genetic disorders based on genotype and phenotype · Bioinform. 2023
Bioinformatics and computational biology › statistical genetics
phenotype-genotype integration
0.712023
diseaseGPS: auxiliary diagnostic system for genetic disorders based on genotype and phenotype · Bioinform. 2023
Bioinformatics and computational biology
genomics
0.212023
diseaseGPS: auxiliary diagnostic system for genetic disorders based on genotype and phenotype · Bioinform. 2023
Bioinformatics and computational biology › statistical genetics
variant prioritization
0.212023
diseaseGPS: auxiliary diagnostic system for genetic disorders based on genotype and phenotype · Bioinform. 2023

Methods — techniques the papers use, named apart from their topics

phenotypic similarity · 0.7ACMG-Bayes · 0.7
YearPublicationVenuePosition
2023 Motivating Online Game Intervention to Enhance Practice Engagement in Children with Functional Articulation Disorder
abstract
The increasing demand for medical services in hospitals has sparked interest in exploring alternative methods to support children with functional articulation disorders. Online speech games have emerged as a promising avenue to motivate children to engage in speech therapy. This study investigates the impact of gamification strategies on children's motivation within the context of speech rehabilitation games. Four distinct game prototypes were developed, with a specific emphasis on stimulating children's motivation to speak. Two sets of experiments involving 48 participants were conducted to assess the influence of (1) time-limitation and (2) interactive imitation objects on children's motivation. The results revealed that time limitation significantly increased motivation, while the effect of imitation objects on motivation was not statistically significant. These findings offer valuable insights into designing effective speech games for children. By leveraging gamification strategies in online speech games, we can address the motivation challenges faced by children with functional articulation disorders and potentially enhance the efficiency of speech therapy interventions.
Naixin Liu, Emilia I. Barakova, Feiran Zhang, Ting Han 0002, Jincai Feng
HAI5
2023 diseaseGPS: auxiliary diagnostic system for genetic disorders based on genotype and phenotype
abstract
SUMMARY: The next-generation sequencing brought opportunities for the diagnosis of genetic disorders due to its high-throughput capabilities. However, the majority of existing methods were limited to only sequencing candidate variants, and the process of linking these variants to a diagnosis of genetic disorders still required medical professionals to consult databases. Therefore, we introduce diseaseGPS, an integrated platform for the diagnosis of genetic disorders that combines both phenotype and genotype data for analysis. It offers not only a user-friendly GUI web application for those without a programming background but also scripts that can be executed in batch mode for bioinformatics professionals. The genetic and phenotypic data are integrated using the ACMG-Bayes method and a novel phenotypic similarity method, to prioritize the results of genetic disorders. diseaseGPS was evaluated on 6085 cases from Deciphering Developmental Disorders project and 187 cases from Shanghai Children's hospital. The results demonstrated that diseaseGPS performed better than other commonly used methods. AVAILABILITY AND IMPLEMENTATION: diseaseGPS is available to freely accessed at https://diseasegps.sjtu.edu.cn with source code at https://github.com/BioHuangDY/diseaseGPS.
Daoyi Huang, Pin Li, Yongfen Lyu, Jincai Feng, Mingyue Wei, Zhixing Zhu, Jianlei Gu, Yongyong Ren, Guangjun Yu, Hui Lu 0004
Bioinform.7