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Agyemang, D.

Publications and source records attributed to Agyemang, D..

2 recordsLinked to original sources

Unique molecular identifiers don't need to be unique: a collision-aware estimator for RNA-seq quantification

RNA-sequencing (RNA-seq) relies on Unique Molecular Identifiers (UMIs) to accurately quantify gene expression after PCR amplification. Longer UMIs minimize collisions--where two distinct transcripts are assigned the same UMI--at the expense of increased sequencing and synthesis costs. However, it is not clear how long UMIs need to be in practice, especially given the nonuniformity of the empirical UMI distribution. In this work, we develop a method-of-moments estimator that accounts for UMI collisions, accurately quantifying gene expression and preserving downstream biological insights. We show that UMIs need not be unique: shorter UMIs can be used with a more sophisticated estimator.

bioinformatics↗

Quantifying Interpretation Reproducibility in Vision Transformer Models with TAVAC

The use of deep learning algorithms to extract meaningful diagnostic features from biomedical images holds the promise to improve patient care given the expansion of digital pathology. Among these deep learning models, Vision Transformer (ViT) models have been demonstrated to capture long-range spatial relationships with more robust prediction power for image classification tasks than regular convolutional neural network (CNN) models, and also better model interpretability. Model interpretation is important for understanding and elucidating how a deep learning model makes predictions, especially for developing transparent models for digital pathology. However, like other deep learning algorithms, with limited annotated biomedical imaging datasets, ViT models are prone to poor performance due to overfitting, which can lead to false predictions due to random noise. Overfitting affects model interpretation when predictions are made out of random noise. To address this issue, we introduce a novel metric - Training Attention and Validation Attention Consistency (TAVAC) - for evaluating ViT model degree of overfitting on imaging datasets and quantifying the reproducibility of interpretation. Specifically, the model interpretation is performed by comparing the high-attention regions in the image between training and testing. We test the method on four publicly available image classification datasets and two independent breast cancer histological image datasets. All overfitted models exhibited significantly lower TAVAC scores than the good-fit models. The TAVAC score quantitatively measures the level of generalization of model interpretation on a fine-grained level for small groups of cells in each H&E image, which cannot be provided by traditional performance evaluation metrics like prediction accuracy. Furthermore, the application of TAVAC extends beyond medical diagnostic AI models; it enhances the monitoring of model interpretative reproducibility at pixel-resolution in basic research, to reveal critical spatial patterns and cellular structures essential to understanding biological processes and disease mechanisms. TAVAC sets a new standard for evaluating the performance of deep learning model interpretation and provides a method for determining the significance of high-attention regions detected from the attention map of the biomedical images.

bioinformatics↗