MAPS: pathologist-level cell type annotation from tissue images through machine learning.
Muhammad ShabanYunhao BaiHuaying QiuShulin MaoJason YeungYao-Yu YeoVignesh ShanmugamHan ChenBokai ZhuJason L WeiratherGarry P NolanMargaret A ShippScott J RodigSizun J JiangFaisal MahmoodPublished in: Nature communications (2024)
Highly multiplexed protein imaging is emerging as a potent technique for analyzing protein distribution within cells and tissues in their native context. However, existing cell annotation methods utilizing high-plex spatial proteomics data are resource intensive and necessitate iterative expert input, thereby constraining their scalability and practicality for extensive datasets. We introduce MAPS (Machine learning for Analysis of Proteomics in Spatial biology), a machine learning approach facilitating rapid and precise cell type identification with human-level accuracy from spatial proteomics data. Validated on multiple in-house and publicly available MIBI and CODEX datasets, MAPS outperforms current annotation techniques in terms of speed and accuracy, achieving pathologist-level precision even for typically challenging cell types, including tumor cells of immune origin. By democratizing rapidly deployable and scalable machine learning annotation, MAPS holds significant potential to expedite advances in tissue biology and disease comprehension.
Keyphrases
- machine learning
- rna seq
- single cell
- big data
- artificial intelligence
- mass spectrometry
- deep learning
- electronic health record
- endothelial cells
- cell therapy
- gene expression
- label free
- induced apoptosis
- amino acid
- high resolution
- stem cells
- protein protein
- cell cycle arrest
- binding protein
- magnetic resonance imaging
- clinical practice
- convolutional neural network
- quantum dots
- risk assessment
- induced pluripotent stem cells
- human health
- signaling pathway
- loop mediated isothermal amplification