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Ruiting Xu

dblp:134/7679 · DBLP profile ↗
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2ranked-venue papers
1as first author
1since 2021 · last 2024
—ORCID · none

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

Artificial intelligence and machine learning · 1Applied, interdisciplinary, general and emerging computing · 1 · 1 first-author · 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 · 100%

Topics — the 1 heaviest of 1, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › transcriptomics
non-coding RNA analysis
0.812024
Improving ncRNA family prediction using multi-modal contrastive learning of sequence and structure · Bioinform. 2024

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

pre-trained language model · 0.8graph neural network · 0.8contrastive learning · 0.8attention mechanism · 0.8
YearPublicationVenuePosition
2024 Improving ncRNA family prediction using multi-modal contrastive learning of sequence and structure
abstract
MOTIVATION: Recent advancements in high-throughput sequencing technology have significantly increased the focus on non-coding RNA (ncRNA) research within the life sciences. Despite this, the functions of many ncRNAs remain poorly understood. Research suggests that ncRNAs within the same family typically share similar functions, underlining the importance of understanding their roles. There are two primary methods for predicting ncRNA families: biological and computational. Traditional biological methods are not suitable for large-scale data prediction due to the significant human and resource requirements. Concurrently, most existing computational methods either rely solely on ncRNA sequence data or are exclusively based on the secondary structure of ncRNA molecules. These methods fail to fully utilize the rich multimodal information available from ncRNAs, thereby preventing them from learning more comprehensive and in-depth feature representations. RESULTS: To tackle these problems, we proposed MM-ncRNAFP, a multi-modal contrastive learning framework for ncRNA family prediction. We first used a pre-trained language model to encode the primary sequences of a large mammalian ncRNA dataset. Then, we adopted a contrastive learning framework with an attention mechanism to fuse the secondary structure information obtained by graph neural networks. The MM-ncRNAFP method can effectively fuse multi-modal information. Experimental comparisons with several competitive baselines demonstrated that MM-ncRNAFP can achieve more comprehensive representations of ncRNA features by integrating both sequence and structural information. This integration significantly enhances the performance of ncRNA family prediction. Ablation experiments and qualitative analyses were performed to verify the effectiveness of each component in our model. Moreover, since our model is pre-trained on a large amount of ncRNA data, it has the potential to bring significant improvements to other ncRNA-related tasks. AVAILABILITY AND IMPLEMENTATION: MM-ncRNAFP and the datasets are available at https://github.com/xuruiting2/MM-ncRNAFP.
Ruiting Xu, Guohua Wang 0001, Yang Li 0130
Bioinform.1
2015 Using fractional order accumulation to reduce errors from inverse accumulated generating operator of grey model
Lifeng Wu 0001, Sifeng Liu, Ligen Yao, Ruiting Xu, Xunping Lei
Soft Comput.4