SPIN-AI: A Deep Learning Model That Identifies Spatially Predictive Genes.
Kevin Meng-LinChoong-Yong UngCheng ZhangTaylor M WeiskittelPhilip WisniewskiZhuofei ZhangShyang-Hong TanKok-Siong YeoShizhen ZhuCristina CorreiaHu LiPublished in: Biomolecules (2023)
Spatially resolved sequencing technologies help us dissect how cells are organized in space. Several available computational approaches focus on the identification of spatially variable genes (SVGs), genes whose expression patterns vary in space. The detection of SVGs is analogous to the identification of differentially expressed genes and permits us to understand how genes and associated molecular processes are spatially distributed within cellular niches. However, the expression activities of SVGs fail to encode all information inherent in the spatial distribution of cells. Here, we devised a deep learning model, Spatially Informed Artificial Intelligence (SPIN-AI), to identify spatially predictive genes (SPGs), whose expression can predict how cells are organized in space. We used SPIN-AI on spatial transcriptomic data from squamous cell carcinoma (SCC) as a proof of concept. Our results demonstrate that SPGs not only recapitulate the biology of SCC but also identify genes distinct from SVGs. Moreover, we found a substantial number of ribosomal genes that were SPGs but not SVGs. Since SPGs possess the capability to predict spatial cellular organization, we reason that SPGs capture more biologically relevant information for a given cellular niche than SVGs. Thus, SPIN-AI has broad applications for detecting SPGs and uncovering which biological processes play important roles in governing cellular organization.
Keyphrases
- artificial intelligence
- bioinformatics analysis
- genome wide
- deep learning
- squamous cell carcinoma
- induced apoptosis
- genome wide identification
- machine learning
- poor prognosis
- big data
- cell cycle arrest
- room temperature
- dna methylation
- density functional theory
- single molecule
- gene expression
- signaling pathway
- single cell
- cell death
- convolutional neural network
- electronic health record
- molecular dynamics
- transcription factor
- social media
- endoplasmic reticulum stress
- rna seq
- data analysis