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Biraaj Rout

Publications and source records attributed to Biraaj Rout.

3 recordsLinked to original sources

Not All Latents Are Equal: Importance-Weighted Latent Graph Generation

Graph generation has shown tremendous effectiveness in modeling complex scientific tasks ranging from molecule generation to optimized circuit design. Most recent advancements have developed models that learn to denoise noisy graphs using either discrete diffusion or flow matching. However, discrete graph diffusion scales quadratically with the number of nodes, making it difficult to use such models on larger graphs. On the other hand, latent graph generation instead seeks to denoise noisy graph latents, which scale better to more nodes due to their lower dimension. However, in practice, latent graph generation models lag behind their discrete counterparts in performance. We study this problem, finding that it is caused by the unequal distribution of that different latent dimensions have on graph reconstruction. the impact. We observe that the vast majority of impact is contained in only a smaller number of latent dimensions. Since equal emphasis is placed on reconstructing the entire latent in the loss function, existing models are optimized to reconstruct information irrelevant to the downstream task. To tackle this problem, we propose Latent Importance Reweighting ({\bf LIR)} which weights each latent dimensions via it's importance to final graph reconstruction. Importance is calculated as the relative influence of a single latent unit on graph reconstruction, which is represented via the Jacobian of the decoder relative to the latent. Our method is model-agnostic and requires no additional model parameters or hyperparameters. Experiments show that LIR can boost performance and lead to faster training convergence when applied to two different autoencoders on various benchmark datasets. Code: https://github.com/biraaj/GraphGenLatentReweight

cs.LG↗

Predicting Future States with Spatial Point Processes in Single Molecule Resolution Spatial Transcriptomics

In this paper, we introduce a pipeline based on XGboost to predict the future distribution of cells that are expressed by the Sog-D gene (active cells) in both the Anterior to posterior (AP) and the Dorsal to Ventral (DV) axis of the Drosophila in embryogenesis process. This method provides insights about how cells and living organisms control gene expression in super resolution whole embryo spatial transcriptomics imaging at sub cellular, single molecule resolution. An XGboost model was used to predict the next stage active distribution based on the previous one. To achieve this goal, we leveraged temporally resolved, spatial point processes by including Ripley's K-function in conjunction with the cell's state in each stage of embryogenesis, and found average predictive accuracy of active cell distribution. This tool is analogous to RNA Velocity for spatially resolved developmental biology, from one data point we can predict future spatially resolved gene expression using features from the spatial point processes.

q-bio.TO↗

The State of Applying Artificial Intelligence to Tissue Imaging for Cancer Research and Early Detection

Artificial intelligence represents a new frontier in human medicine that could save more lives and reduce the costs, thereby increasing accessibility. As a consequence, the rate of advancement of AI in cancer medical imaging and more particularly tissue pathology has exploded, opening it to ethical and technical questions that could impede its adoption into existing systems. In order to chart the path of AI in its application to cancer tissue imaging, we review current work and identify how it can improve cancer pathology diagnostics and research. In this review, we identify 5 core tasks that models are developed for, including regression, classification, segmentation, generation, and compression tasks. We address the benefits and challenges that such methods face, and how they can be adapted for use in cancer prevention and treatment. The studies looked at in this paper represent the beginning of this field and future experiments will build on the foundations that we highlight.

q-bio.TO↗