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Biology subjects

Ting, W.

Publications and source records attributed to Ting, W..

2 recordsLinked to original sources

Research on Crop Phenotype Prediction Methods Based on SNP-context and Whole-genome Features Embedding

Modern agriculture demands precise genomic prediction to accelerate elite crop breeding, yet traditional genomic prediction approaches, such as genomic best linear unbiased prediction (GBLUP) and Bayesian methods, focus primarily on the cumulative effect of individual SNPs, thus neglecting the concerted influence that the surrounding sequence context has on the phenotype. To overcome these limitations, we propose two novel feature embedding modes (SNP-context and whole-genome) based on DNABERT-2, a cross-species genomic foundation model that uses self-attention mechanisms and transfer learning to automatically identify conserved sequence features across diverse evolutionary lineages without prior biological assumptions. The whole-genome feature embedding aggregates genomic information at a global scale by pooling vectors from chunked sequences processed by DNABERT-2, whereas the context feature embedding captures local information by directly encoding variable-length (500--3000 bp) sequences centered on target SNPs. To reduce noise in the high-dimensional feature embeddings, we employed principal component analysis (PCA) and partial least squares (PLS) to project the features into a lower-dimensional space. We generated two kinds of feature embedding for three crop datasets (rice413, rice395, and maize301), investigated the impact of 500--3000 bp flanking SNP contexts on phenotypic prediction, and compared prediction accuracy variations across algorithms at 4--768 feature dimensions among the PCA, PLS, and no dimensionality reduction strategies. The results demonstrate that machine learning (ML) algorithms operating under the SNP-context embedding mode achieve greater accuracy and lower mean absolute errors (MAEs) than traditional SNP features do at specific context lengths, particularly for traits with low-to-moderate heritability (h2[isin](0.2, 0.7]). In contrast, using whole-genome embeddings as input for ML can further improve the prediction accuracy for highly heritable traits (h2[isin](0.7, 1.0]), even outperforming state-of-the-art deep learning models (such as DNNGP and ResGS) that rely on SNP markers. Our code is available on https://github.com/oliveSpring/Crop_DNA_Embedding.git

genetics↗

Spatially resolved molecular and cellular atlas of the mouse brain

A comprehensive atlas of genes, cell types, and their spatial distribution across a whole mammalian brain is fundamental for understanding function of the brain. Here, using snRNA-seq and Stereo-seq techniques, we generated a mouse brain atlas with spatial information for 308 cell clusters with single-cell resolution involving over 6 million cells as well as for 29,655 genes. We have identified new astrocyte clusters, and demonstrated that distinct cell clusters exhibit preference for cortical subregions. In addition, we identified 155 genes exhibiting regional specificity in the brainstem, and 513 long non-coding RNA exhibited regional specificity in the adult brain. Parcellation of brain regions based on spatial transcriptomic information showed large overlap with that by traditional method. Furthermore, we have uncovered 411 transcription factor regulons with spatiotemporal specificity during development. Thus, our study has discovered genes and regulon with spatiotemporal specificity, and provided a high-resolution spatial transcriptomic atlas of the mouse brain.

neuroscience↗