Search bioRxiv⌕ Search

Biology subjects

Dajani, R.

Publications and source records attributed to Dajani, R..

3 recordsLinked to original sources

BioVault: A privacy-first data visitation platform for equitable global collaboration in biomedicine

Biomedical datasets representing diverse populations are essential for advancing precision medicine, yet remain siloed due to regulatory, sovereignty, and privacy constraints. Existing data-sharing solutions remain limited. Centralized repositories and Trusted Research Environments (TREs) require data migration into external infrastructure, introducing governance complexities, cost barriers, and constraints on accountable reuse. Secure computation frameworks from modern cryptography, and federated learning models demand deep domain expertise and substantial engineering effort, limiting their accessibility in resource-constrained environments. These barriers disproportionately impact under-resourced institutions, limiting equitable participation in global collaborations. Here, we introduce BioVault (https://www.biovault.net), an open-source platform for privacy-first biomedical collaboration through a peer-to-peer data visitation network, where analysis code travels to data rather than data being transferred to centralized systems. BioVault can be deployed as a desktop application or command-line interface, enabling out-of-the-box use for participants in diverse resource settings. BioVault supports both clinical and research workflows, and with built-in permissioning, audit trails, and local governance controls, it enables data holders and collaborators to retain oversight and control while participating in collaborative research. We demonstrate BioVaults utility in enabling two cross-border collaborations with under-resourced communities: a genome-wide association study of Type 2 Diabetes in Circassian and Chechen populations in Jordan, and allele frequency estimation across Caribbean cohorts. In both cases, analyses were executed locally without data export. We further demonstrate compatibility for user-defined secure, federated computation protocols built on state-of-the-art cryptographic tools (multiparty computation and homomorphic encryption), by lowering barriers to their deployment. Together, these results establish BioVault as a general-purpose framework for decentralized analytics that reduces the technical and financial constraints to biomedical collaboration - enabling diverse institutions to participate as equal partners in global discovery, while preserving privacy and data sovereignty.

genomics↗

Deciphering regulation of FOXP3 expression in human conventional T cells

FOXP3 is a lineage-defining transcription factor (TF) for immune-suppressive regulatory T cells (Tregs). While mice exclusively express FOXP3 in Tregs, humans also transiently express FOXP3 in stimulated conventional CD4+ T cells (Tconvs). Mechanisms governing these distinct expression patterns remain unknown. Here, we performed CRISPR screens tiling the FOXP3 locus and targeting TFs in human Tregs and Tconvs to discover cis-regulatory elements (CREs) and trans-regulators of FOXP3. Tconv FOXP3 expression depended on a subset of Treg CREs and Tconv-selective positive (TcNS+) and negative (TcNS-) CREs. The CREs are occupied and regulated by TFs we identified as critical regulators of FOXP3. Finally, mutagenesis of murine TcNS- revealed that it is critical for restriction of FOXP3 expression to Tregs. We discover CRE and TF circuitry controlling FOXP3 expression and reveal evolution of mechanisms regulating a gene indispensable to immune homeostasis. HighlightsO_LIComprehensive CRISPR maps of CREs and TFs controlling FOXP3 in human Tregs and Tconvs C_LIO_LIKey TFs that control FOXP3 directly occupy and regulate CREs forming TF-CRE circuits C_LIO_LIA previously unknown negative CRE stringently restricts FOXP3 to Tregs in mice C_LI

immunology↗

FAAH, SLC6A4, and BDNF variants are not associated with psychosocial stress and mental health outcomes in a population of Syrian refugee youth

The developmental origins of health and disease (DOHaD) hypothesis posits that early childhood stressors disproportionately impact adult health. Numerous studies have found adult mental health to be associated with childhood adversities and genetic variants, particularly in genes related to neurochemistry. However, few studies have examined the way interactive effects may manifest over time and fewer still include protective factors, like resilience. Our group has previously found associations between the monoamine oxidase A gene, MAOA, and a contextually-specific measure of resilience with a measure of perceived psychosocial stress over time in Syrian refugee youth. In this study, we work with the same sample of adolescents to test genetic variants in three additional candidate genes (FAAH, the 5-HTTLPR region of SLC6A4, and BDNF) for associations with six psychosocial stress and mental health outcomes. Using multi-level modeling, we find no association between variants in these candidate genes and psychosocial stress or mental health outcomes. Our analysis included tests for both direct genetic effects and interactions with lifetime trauma and resilience. Negative results, such as the lack of genetic associations with outcome measures, provides a more complete framework in which to better understand positive results and associations.

genetics↗