Top-k discriminative feature selection with uncorrelated and ℓ2,0-norm equation constraints

判别式 特征选择 不相关 计算机科学 选择(遗传算法) 人工智能 模式识别(心理学) 数学 统计
作者
Jingyu Wang,Zhenyu Ma,Feiping Nie,Xuelong Li
出处
期刊:Neurocomputing [Elsevier]
卷期号:598: 128069-128069
标识
DOI:10.1016/j.neucom.2024.128069
摘要

Supervised feature selection (FS) as an interpretable dimensionality reduction technique has received increasing attention, where linear discriminative analysis (LDA)-based method can select informative features discriminatively and obtain promising performance. When original data has more features than samples, however, LDA-based method generally encounters degradation since the appearance of irreversible scatter matrix. This situation is called the small sample size (SSS) problem. To overcome it and enhance the discriminant power of selected feature subsets, in this paper, we design an elegant LDA-based FS model referred to as Top-k Discriminative FS (TDFS), which is constructed by seamlessly integrating the ℓ2,0-norm equation constraint into uncorrelated LDA model. More concretely, the ℓ2,0-norm equation constraint can explicitly characterize the number of selective features k to ensure the sparsity of projected matrix and select top features. The uncorrelated LDA model aims to improve discriminative ability based on uncorrelated data in projected subspace. Given the formidable nature of solving this non-convex model, a novel optimization algorithm is further developed and the SSS problem can be efficaciously addressed during the optimization process. We first decompose projection matrix into a discrete selection matrix and its corresponding nonzero projection matrix, then concurrently optimize above two matrices by employing a column-by-column update scheme, during which the reversibility of scatter matrix in selective feature subspace can be easily guaranteed to solve SSS problem. The extensive experiments on four synthetic data sets and eight real-world data sets show that the proposed method outperforms eight competitors validated by three classifiers. Moreover, although the theoretical analysis proves that our algorithm has quartic time complexity on the number of selected features k, the running time experiments verify that TDFS is still efficient and applicable in scenarios where only a small number of features need to be selected. From above perspectives, our algorithm shows desirable performance to achieve discriminative FS.

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
落后的山水完成签到,获得积分10
2秒前
欢呼的书南完成签到,获得积分10
3秒前
田様应助小瓦片采纳,获得10
3秒前
不知道叫个啥完成签到 ,获得积分10
5秒前
气人的刘大妈完成签到,获得积分10
6秒前
8秒前
8秒前
8秒前
9秒前
科研通AI2S应助曦月采纳,获得10
11秒前
feishao完成签到,获得积分10
11秒前
replay完成签到,获得积分20
11秒前
11秒前
12秒前
niu完成签到,获得积分10
14秒前
16秒前
斯文败类应助gaobowang采纳,获得10
19秒前
20秒前
chun123完成签到,获得积分20
21秒前
冷酷夜绿发布了新的文献求助10
21秒前
深情安青应助科研通管家采纳,获得10
21秒前
思源应助科研通管家采纳,获得10
21秒前
爆米花应助科研通管家采纳,获得10
21秒前
21秒前
无敌小宽哥应助日升月采纳,获得10
23秒前
深情安青应助源源采纳,获得10
23秒前
Tink完成签到,获得积分10
24秒前
吃土少年发布了新的文献求助10
25秒前
26秒前
26秒前
可爱的函函应助科研小白采纳,获得30
26秒前
27秒前
故里完成签到,获得积分10
28秒前
无敌小宽哥应助yx采纳,获得10
28秒前
酷波er应助Danqi采纳,获得10
29秒前
Ariel完成签到,获得积分10
31秒前
zzzzzzzzzzzz发布了新的文献求助10
31秒前
深情安青应助wp采纳,获得10
31秒前
31秒前
高分求助中
Evolution 2024
Impact of Mitophagy-Related Genes on the Diagnosis and Development of Esophageal Squamous Cell Carcinoma via Single-Cell RNA-seq Analysis and Machine Learning Algorithms 2000
Experimental investigation of the mechanics of explosive welding by means of a liquid analogue 1060
Die Elektra-Partitur von Richard Strauss : ein Lehrbuch für die Technik der dramatischen Komposition 1000
How to Create Beauty: De Lairesse on the Theory and Practice of Making Art 1000
Gerard de Lairesse : an artist between stage and studio 670
CLSI EP47 Evaluation of Reagent Carryover Effects on Test Results, 1st Edition 600
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3006183
求助须知:如何正确求助?哪些是违规求助? 2665373
关于积分的说明 7226641
捐赠科研通 2302402
什么是DOI,文献DOI怎么找? 1220755
科研通“疑难数据库(出版商)”最低求助积分说明 594878
版权声明 593314