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Biology subjects

Simmonds, S. E.

Publications and source records attributed to Simmonds, S. E..

3 recordsLinked to original sources

A Cross-Species Generative Cell Atlas Across 1.5 Billion Years ofEvolution: The TranscriptFormer Single-cell Model

Single-cell transcriptomics has revolutionized our understanding of cellular diversity, yet our understanding of the transcriptional programs across the tree of life remains limited. Here we present TranscriptFormer, a family of generative foundation models trained on up to 112 million cells spanning 1.53 billion years of evolution across 12 species. By jointly modeling gene identities and expression levels using a novel generative architecture, TranscriptFormer encodes multi-scale biological structure, functioning as a queryable virtual cell atlas. We demonstrate state-of-the-art performance on both in-distribution and out-of-distribution cell type classification, with robust performance even for species separated by over 685 million years of evolution. TranscriptFormer can also perform zero-shot disease state identification in human cells and accurately transfers cell state annotations across species boundaries. As a generative model, TranscriptFormer can be prompted to predict cell type-specific transcription factors and gene-gene interactions that align with independent experimental observations. Developmental trajectories, phylogenetic relationships and cellular hierarchies emerge naturally in TranscriptFormers representations without any explicit training on these annotations. This work establishes a powerful framework for quantitative single-cell analysis, and comparative cellular biology, thus demonstrating that universal principles of cellular organization can be learned and predicted across the tree of life.

systems biology↗

CZ ID: a cloud-based, no-code platform enabling advanced long read metagenomic analysis

Metagenomics has enabled the rapid, unbiased detection of microbes across diverse sample types, leading to exciting discoveries in infectious disease, microbiome, and viral research. However, the analysis of metagenomic data is often complex and computationally resource-intensive. CZ ID is a free, cloud-based genomic analysis platform that enables researchers to detect microbes using metagenomic data, identify antimicrobial resistance genes, and generate viral consensus genomes. With CZ ID, researchers can upload raw sequencing data, find matches in NCBI databases, get per-sample taxon metrics, and perform a variety of analyses and data visualizations. The intuitive interface and interactive visualizations make exploring and interpreting results simple. Here, we describe the expansion of CZ ID with a new long read mNGS pipeline that accepts Oxford Nanopore generated data (czid.org). We report benchmarking of a standard mock microbial community dataset against Kraken2, a widely used tool for metagenomic analysis. We evaluated the ability of this new pipeline to detect divergent viruses using simulated datasets. We also assessed the detection limit of a spiked-in virus to a cell line as a proxy for clinical samples. Lastly, we detected known and novel viruses in previously characterized disease vector (mosquitoes) samples.

bioinformatics↗

Seascape genomics reveals population structure and local adaptation in a widespread coral reef snail, Coralliophila violacea (Kiener, 1836)

Local adaptation to different environments may reinforce neutral evolutionary divergence, especially in populations in the periphery of a species geographic range. Seascape genomics (high-throughput genomics coupled with ocean climate databases) facilitates the exploration of neutral and adaptive variation in concert, developing a clearer picture of processes driving local adaptation in marine populations. This study used a seascape genomics approach to test the relative roles of neutral and adaptive processes shaping population divergence of a widespread coral reef snail, Coralliophila violacea. We collected C. violacea from colonies of their coral host (Porites spp.) at ten locations spanning a large portion of their geographic range. We used RAD-seq to investigate possible local adaptation via genetic-environmental associations with five ocean climate variables. Four genetic partitions were concordant with regions previously observed in mtDNA (Indian Ocean, Coral Triangle, and Hawaiian Islands), with the addition of Vietnam and varying isolation and admixture levels. We identified outlier loci (FDR = 0.10, N = 72) among individual localities and between regions (FDR = 0.10, N = 34), suggesting that some loci are putatively under divergent selection. Association analyses showed that the two strongest drivers of local adaptation were the annual range and mean of sea surface temperature. Populations that experience lower sea surface temperatures at the periphery of C. violaceas geographic range drive these associations. Our results show that local adaptation to different environments likely reinforces neutral divergence, especially in peripheral populations.

evolutionary biology↗