Driven by medical radiomics and high-throughput techniques, there has been explosive growth in the amount of advanced multiomics data in modern biomedical research. These data contain abundant information reflecting cellular context, allowing researchers to disentangle biomolecular mechanisms, and gain a more comprehensive understanding of biological processes related to complex diseases. [1,2] Single-omics data provide limited information on biological systems. The systematic study of biomedical objects by integrating and analyzing data at diverse scales is an emerging field. [3][4][5] The integration of multiomics data makes it possible to understand complex biological systems from different perspectives. [5,6] Using multiomics data can identify the best therapeutic targets and address key biomedical objects, including personalized complex disease therapy, [7][8][9][10][11] drug discovery, [12][13][14][15] and drug target discovery. [16][17][18][19][20] However, multiomics data are complex, high dimensional, and heterogeneous. [21,22] By far the most important challenge is how to extract valuable knowledge from these data. Since various omics data are obtained by different measurement techniques, the data distribution for different omics is different. The inconsistency of data distribution is one of the difficulties to be overcome. At the same time, each sample contains data from multiple omics, and exploring potential correlations between these data is also a problem. Biomedical data is also characterized by high dimensionality and few samples, which can generate the curse of dimensionality during data mining and reduce the generalization ability of the model. To address this challenge, researchers have developed methods such as multiple kernel learning, Bayesian approaches, dimensionality reduction approaches, network-based methods, and deep learning (DL) methods. [23][24][25][26][27][28][29][30] With the continuous development of DL, up to now, many DL methods have emerged to integrate multiomics data. The DL methods can be utilized as an efficient framework to process a large amount of multiomics, high-dimensional, and complex data. The DL-based methods can capture the typical nonlinearities and complex relationships in biological data to achieve more accurate predictions. DL, represented by multiomics data modeling, has achieved substantial success in biomedical fields. The combination of DL and multiomics data is significantly beneficial for the development of modern biomedical studies.In this article, we mainly focused on how to effectively extract omics data representations and how to integrate these representations. We classified multiomics integration models into six categories according to the framework of DL-based multiomics data integration methods. In addition, we reviewed and