Master Explainable AI (XAI) for Single-Cell Multi-Omics Integration in 4 weeks through hands-on, project-based online training with DSTC.
Multi-omics data integration at the single-cell level is revolutionizing our understanding of cellular heterogeneity, disease mechanisms, and therapeutic response. However, integrating high-dimensional datasets from different omics layers (e.g., genomics, transcriptomics, proteomics, epigenomics) presents significant challenges, particularly in terms of model interpretability and biological relevance. Explainable AI (XAI) methods are essential in providing transparency into the complex AI models used to analyze such data, ensuring that results are not only accurate but also biologically interpretable. Every participant receives a verified e-Certificate and e-Marksheet from the Deep Science & Technology Consortium.
Multi-omics data integration at the single-cell level is revolutionizing our understanding of cellular heterogeneity, disease mechanisms, and therapeutic response. However, integrating high-dimensional datasets from different omics layers (e.g., genomics, transcriptomics, proteomics, epigenomics) presents significant challenges, particularly in terms of model interpretability and biological relevance. Explainable AI (XAI) methods are essential in providing transparency into the complex AI models used to analyze such data, ensuring that results are not only accurate but also biologically interpretable.
1. Put biotechnology techniques to work on real datasets and case studies.
2. Build a defensible project you can showcase to supervisors, reviewers, or employers.
β’ Master's and senior undergraduate students specializing in biotechnology
β’ R&D engineers and working professionals applying biotechnology in industry
β’ Academics and educators building research or teaching capacity in biotechnology
β’ Tangible, reproducible biotechnology work to show supervisors or employers.
β’ A verified e-Certificate of competency and e-Marksheet from the Deep Science & Technology Consortium.
β’ scRNA-seq, scATAC-seq and CITE-seq: what each measures and its sparsity
β’ Doublets, ambient RNA and dropout as technical confounders
β’ Paired versus unpaired multi-omic designs
β’ Batch correction and integration methods, and their over-correction risk
β’ Autoencoder and factor-model approaches to joint embedding
β’ Evaluating integration without a ground-truth alignment
β’ Attribution to genes, peaks and proteins driving a latent dimension
β’ Attention and gradient methods and their instability on sparse counts
β’ Distinguishing biological signal from technical covariate
β’ Marker-based sanity checks against known cell biology
β’ Perturbation and held-out validation of proposed mechanisms
β’ Reporting uncertainty in cell-type and state assignment
β’ Regulatory inference linking accessibility to expression
β’ Trajectory and state-transition interpretation, and its assumptions
β’ Communicating an explainable result to experimental collaborators
| Parameter | Requirement |
|---|---|
| Covered Tool / Platform | Python |
| Covered Tool / Platform | TensorFlow |
| Covered Tool / Platform | PyTorch |
| Covered Tool / Platform | Keras |
| Covered Tool / Platform | Scikit-learn |
| Covered Tool / Platform | Jupyter Notebook |
| Covered Tool / Platform | Google Colab |
| Covered Tool / Platform | Hugging Face |
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