In a heterogeneous unreliable multiaccess network, wherein terminals share a common wireless channel with distinct error probabilities, existing works have shown that a persistent round-robin (RR-P) scheduling policy can be arbitrarily worse than the optimum in terms of Age of Information (AoI) under standard Automatic Repeat reQuest (ARQ). In this paper, practical Hybrid ARQ (HARQ) schemes which are widely-used in today's wireless networks are considered. We show that RR-P is very close to optimum with asymptotically many terminals in this case, by explicitly deriving tight, closed-form AoI gaps between optimum and achievable AoI by RR-P. In particular, it is rigorously proved that for RR-P, under HARQ models concerning fading channels (resp. finite-blocklength regime), the relative AoI gap compared with the optimum is within a constant of 6.4% (resp. 6.2% with error exponential decay rate of 0.5). In addition, RR-P enjoys the distinctive advantage of implementation simplicity with channel-unaware and easy-to-decentralize operations, making it favorable in practice. A further investigation considering constraint imposed on the number of retransmissions is presented. The performance gap is indicated through numerical simulations.

Recent studies in protein structure prediction such as AlphaFold have enabled deep learning to achieve great attention on the Drug-Target Affinity (DTA) task. Most works are dedicated to embed single molecular property and homogeneous information, ignoring the diverse heterogeneous information gains that are contained in the molecules and interactions. Motivated by this, we propose an end-to-end deep learning framework to perform Molecular Heterogeneous features Fusion (MolHF) for DTA prediction on heterogeneity. To address the challenges that biochemical attributes locates in different heterogeneous spaces, we design a Molecular Heterogeneous Information Learning module with multi-strategy learning. Especially, Molecular Heterogeneous Attention Fusion module is present to obtain the gains of molecular heterogeneous features. With these, the diversity of molecular structure information for drugs can be extracted. Extensive experiments on two benchmark datasets show that our method outperforms the baselines in all four metrics. Ablation studies validate the effect of attentive fusion and multi-group of drug heterogeneous features. Visual presentations demonstrate the impact of protein embedding level and the model ability of fitting data. In summary, the diverse gains brought by heterogeneous information contribute to drug-target affinity prediction.

This letter addresses the problem of space-time adaptive processing (STAP) for airborne nonuniform linear array (NLA) radar using a generalized sidelobe canceller (GSC). Due to the difficulty of determining the spatial nulls for the NLAs, it is a problem to obtain a valid blocking matrix (BM) of the GSC directly. In order to solve this problem and improve the STAP performance, a BM modification method based on the modified Gram-Schmidt orthogonalization algorithm is proposed. The modified GSC processor can achieve the optimal STAP performance and as well a faster convergence rate than the orthogonal subspace projection method. Numerical simulations validate the effectiveness of the proposed methods.