Shabnam Kasra Kermanshahi

Amirmohammad Pasdar, Shabnam Kasra Kermanshahi, Nour Moustafa et al.

The Internet of Battlefield Things (IoBT) relies on heterogeneous, bandwidth-constrained, and intermittently connected tactical networks that face rapidly evolving cyber threats. In this setting, intrusion detection cannot depend on continuous central collection of raw traffic due to disrupted links, latency, operational security limits, and non-IID traffic across zones. We present Zone-Adaptive Intrusion Detection (ZAID), a collaborative detection and model-improvement framework for unseen attack types, where "zero-day" refers to previously unobserved attack families and behaviours (not vulnerability disclosure timing). ZAID combines a universal convolutional model for generalisable traffic representations, an autoencoder-based reconstruction signal as an auxiliary anomaly score, and lightweight adapter modules for parameter-efficient zone adaptation. To support cross-zone generalisation under constrained connectivity, ZAID uses federated aggregation and pseudo-labelling to leverage locally observed, weakly labelled behaviours. We evaluate ZAID on ToN_IoT using a zero-day protocol that excludes MITM, DDoS, and DoS from supervised training and introduces them during zone-level deployment and adaptation. ZAID achieves up to 83.16% accuracy on unseen attack traffic and transfers to UNSW-NB15 under the same procedure, with a best accuracy of 71.64%. These results indicate that parameter-efficient, zone-personalised collaboration can improve the detection of previously unseen attacks in contested IoBT environments.

Sara Jafarbeiki, Raj Gaire, Amin Sakzad et al.

The cost of DNA sequencing has resulted in a surge of genetic data being utilised to improve scientific research, clinical procedures, and healthcare delivery in recent years. Since the human genome can uniquely identify an individual, this characteristic also raises security and privacy concerns. In order to balance the risks and benefits, governance mechanisms including regulatory and ethical controls have been established, which are prone to human errors and create hindrance for collaboration. Over the past decade, technological methods are also catching up that can support critical discoveries responsibly. In this paper, we explore regulations and ethical guidelines and propose our visions of secure/private genomic data storage/processing/sharing platforms. Then, we present some available techniques and a conceptual system model that can support our visions. Finally, we highlight the open issues that need further investigation.

Sara Jafarbeiki, Amin Sakzad, Shabnam Kasra Kermanshahi et al.

Searchable symmetric encryption (SSE) has been used to protect the confidentiality of genomic data while providing substring search and range queries on a sequence of genomic data, but it has not been studied for protecting single nucleotide polymorphism (SNP)-phenotype data. In this article, we propose a novel model, PrivGenDB, for securely storing and efficiently conducting different queries on genomic data outsourced to an honest-but-curious cloud server. To instantiate PrivGenDB, we use SSE to ensure confidentiality while conducting different types of queries on encrypted genomic data, phenotype and other information of individuals to help analysts/clinicians in their analysis/care. To the best of our knowledge, PrivGenDB construction is the first SSE-based approach ensuring the confidentiality of shared SNP-phenotype data through encryption while making the computation/query process efficient and scalable for biomedical research and care. Furthermore, it supports a variety of query types on genomic data, including count queries, Boolean queries, and k'-out-of-k match queries. Finally, the PrivGenDB model handles the dataset containing both genotype and phenotype, and it also supports storing and managing other metadata like gender and ethnicity privately. Computer evaluations on a dataset with 5,000 records and 1,000 SNPs demonstrate that a count/Boolean query and a k'-out-of-k match query over 40 SNPs take approximately 4.3s and 86.4μs, respectively, that outperforms the existing schemes.