bioRxiv Science⌕ Search

Biology subjects

Waldhaus, J.

Publications and source records attributed to Waldhaus, J..

2 recordsLinked to original sources

Developing a general AI model for integrating diverse genomic modalities and comprehensive genomic knowledge

Advances in next-generation sequencing technologies have vastly expanded the availability of diverse genomic, epigenomic and transcriptomic data, presenting the opportunity to develop a general AI model that integrates comprehensive genomic knowledge into a unified model. Unlike previous predictive models, which are typically specialized to certain tasks, our general AI model unifies a wide range of genomic modalities, such as nascent RNA and ultra-high-resolution chromatin organization, within a multi-task architecture. Using ATAC-seq and DNA sequences as inputs, we incorporated diverse genomic modalities as output, and the model exhibits strong generalizability across different cell types and tissues in all tasks we trained. It accurately predicts gene-level transcription measured by various nascent RNA assays, and effectively captures enhancer-associated transcription. Additionally, it also accurately captures the potential functions of non-coding genetic variants and regulatory elements. Additionally, we extended the model trained on human data to a mouse general model, achieving accurate predictions of genomic modalities, such as high resolution chromatin contact maps with limited data availability, which are further validated using an established mouse inner-ear study. This comprehensive approach offers a powerful tool for understanding genome regulation in both human and mouse species.

bioinformatics↗

Mapping the developmental potential of mouse inner ear organoids at single-cell resolution

Inner ear organoids recapitulate development and are intended to generate cell types of the otic lineage for applications such as basic science research and cell replacement strategies. Here, we use single-cell sequencing to study the cellular heterogeneity of late-stage mouse inner ear organoid sensory epithelia, which we validated by comparison with data sets of the mouse cochlea and vestibular epithelia. We resolved supporting cell sub-types, cochlear like hair cells, and vestibular Type I and Type II like hair cells. While cochlear like hair cells aligned best with an outer hair cell trajectory, vestibular like hair cells followed developmental trajectories similar to in vivo programs branching into Type II and then Type I extrastriolar hair cells. These results highlight the transcriptional accuracy of the organoid developmental program but will also inform future strategies to improve synaptic connectivity and regional specification.

developmental biology↗