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Biology subjects

Czech, E.

Publications and source records attributed to Czech, E..

6 recordsLinked to original sources

GeneCAD: Plant Genome Annotation with a DNA Foundation Model

Accurate genome annotation is fundamental to biological discovery, yet identifying gene structures directly from DNA sequence remains a major challenge in complex genomes. We introduce GeneCAD, a sequence-only framework that predicts biologically coherent gene models without requiring species-matched transcriptomic or proteomic evidence. GeneCAD integrates lineage-specific DNA representations from the PlantCAD2 foundation model with a transformer encoder and a chromosome-scale conditional random field (CRF) to enforce structural constraints, such as splice-phase and feature order. To ensure high-quality supervision, we implement a curation strategy using a sequence-based masked-motif score to filter reference transcripts. As a primary validation across diverse angiosperms, including a complex allotetraploid, GeneCAD improves transcript F1 by approximately 9% over current tools like Helixer and BRAKER3, while sharpening boundary precision and achieving a best-in-class recovery of 86% of classical coding sequences. Furthermore, we demonstrate the frameworks modularity by adapting it to animal lineages through the substitution of the underlying DNA foundation model. While the long introns of vertebrates challenge full transcript reconstruction, the model remains highly effective at identifying individual exons. By connecting evolutionary signals with structured decoding, GeneCAD provides a versatile and scalable solution for high-fidelity genome annotation across the Tree of Life. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=102 SRC="FIGDIR/small/685877v3_ufig1.gif" ALT="Figure 1"> View larger version (33K): org.highwire.dtl.DTLVardef@5dd348org.highwire.dtl.DTLVardef@1da37daorg.highwire.dtl.DTLVardef@188ef17org.highwire.dtl.DTLVardef@108da0c_HPS_FORMAT_FIGEXP M_FIG C_FIG Lay SummaryIdentifying where genes are located within a genome is a major challenge in biology, especially in plants with large and repetitive DNA. Current methods often rely on expensive laboratory data or struggle to find genes in "noisy" regions. We developed GeneCAD, a deep-learning tool that identifies genes using only the raw DNA sequence. By using AI models that recognize patterns shaped by millions of years of evolution, GeneCAD predicts gene structures with high accuracy and consistency. Our tests show that GeneCAD outperforms existing tools in plants and can be easily adapted for use in other species, including animals. By removing the need for costly lab experiments, GeneCAD provides an affordable way for researchers to quickly map the genomes of everything from rare wild plants to essential food crops.

bioinformatics↗

PlantCAD2: A Long-Context DNA Language Model for Cross-Species Functional Annotation in Angiosperms

Understanding how DNA sequence encodes biological function remains a fundamental challenge in biology. Flowering plants (angiosperms), the dominant terrestrial clade, exhibit maximal biochemical complexity, extraordinary species diversity (over 100,000 species), relatively recent origins ([~]160 million years), [~]200-fold variation in genome size and relative compact coding regions compared with other eukaryotes. These features present both a unique challenge and opportunity for pre-training DNA language models to understand plant-specific evolutionary conservation, regulatory architectures and genomic functions. Here, we introduce PlantCAD2, an extended context, plant-specific DNA language model with single-nucleotide resolution, pre-trained on 65 angiosperm genomes, together with a series of public benchmarks for evaluation. Comprehensive zero-shot testing shows that PlantCAD2 (676 million parameters) efficiently captures evolutionary conservation, surpassing the 7-billion-parameter Evo2 model in 10 of 12 tasks. With parameter-efficient fine-tuning, PlantCAD2 also outperforms the 1-billion-parameter AgroNT across seven cross-species tasks including chromatin accessible region, gene expression and protein translation. Moreover, its 8,192bp context window substantially improves accessible chromatin prediction in large genomes such as maize (AUPRC increasing from 0.587 to 0.711), underscoring the importance of long-range context for modeling distal regulation. Together, these results establish PlantCAD2 as a powerful, efficient, and versatile foundation model for plant genomics, enabling accurate genome annotation across diverse species.

bioinformatics↗

Towards a scaled-up T cell-mediated cytotoxicity assay in 3D cell culture using microscopy

Three-dimensional (3D) cell culture systems with tumor spheroids are being adopted for research on the antitumor activity of drug treatments and cytotoxic T cells. Analysis of the cytotoxic effect on 3D tumor cultures within a 3D scaffold, such as collagen, is challenging. Image-based approaches often use confocal microscopy, which greatly limits the sample size of tumor spheroids that can be assayed. We explored a system where tumor spheroids growing in a collagen gel within a microfluidics chip can be treated with drugs or co-cultured with T cells. We attempted to adapt the system to measure the death of cells in the tumor spheroids directly in the microfluidics chip via automated widefield fluorescence microscopy. We were able to successfully measure drug-induced cytotoxicity in tumor spheroids, but had difficulties extending the system to measure T cell-mediated tumor killing. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=193 SRC="FIGDIR/small/842039v1_ufig1.gif" ALT="Figure 1"> View larger version (44K): org.highwire.dtl.DTLVardef@c95725org.highwire.dtl.DTLVardef@785728org.highwire.dtl.DTLVardef@a23dceorg.highwire.dtl.DTLVardef@187bd74_HPS_FORMAT_FIGEXP M_FIG C_FIG

immunology↗

Computational and experimental optimization of T cell activation

Bead-based activation is widely-used for ex vivo expansion of T cells for either research or clinical purposes. Despite its wide use, culture conditions that can potentially affect the efficiency of bead-based T cell activation has not been extensively documented. With the help of computationally-driven experimental investigations of basic culturing factors, we found that culture density, bead-to-cell ratio, and debeading time can have a major impact on the efficiency of bead-based T cell activation for short-term cultures. Furthermore, discrepancies across expected and observed activation efficiencies helped discover interesting artifacts of bead-based T cell activation.\n\n\n\nO_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=152 SRC=\"FIGDIR/small/629857v1_ufig1.gif\" ALT=\"Figure 1\">\nView larger version (104K):\norg.highwire.dtl.DTLVardef@107140corg.highwire.dtl.DTLVardef@1b52475org.highwire.dtl.DTLVardef@16c95cborg.highwire.dtl.DTLVardef@1de5184_HPS_FORMAT_FIGEXP M_FIG Human primary T cells were imaged together with activation beads at 20X magnification after three hours of culturing at varying confluencies and bead-to-cell ratios.\n\nC_FIG

immunology↗

Electroporation characteristics of human primary T cells

Electroporation is the most feasible non-viral material delivery system for manipulating human T cells given its time- and cost-effectiveness. However, efficient delivery requires electroporation settings to be optimized for different devices, cellular states, and materials to be delivered. Here, we used electroporation to either induce exogenous gene expression in human primary T cells by plasmids or in vitro transcribed (IVT) mRNA and also target endogenous genes by Cas9 ribonucleoproteins (RNPs). We characterized the electroporation conditions both for activated and unstimulated human T cells. Although naive cells are non-dividing and therefore their genetic manipulation is harder compared to activated T cells, we developed the technical ability to manipulate both naive and memory cells within the unstimulated T cell population by IVT mRNA and Cas9 RNP electroporation. Here, we outline the best practices for achieving highly-efficient genetic manipulation in primary T cells without causing significant cytotoxicity to the cells. Because there is increasing evidence for \"less-differentiated\" T cells to have better anti-tumor activity for immunotherapy, manipulating naive T cells with high efficiency is also of high importance to clinical applications and to study the biology of these cells.

immunology↗

Cytokit: A single-cell analysis toolkit for high dimensional fluorescent microscopy imaging

BackgroundMultiplexed in-situ fluorescent imaging offers several advantages over single-cell assays that do not preserve the spatial characteristics of biological samples. This spatial information, in addition to morphological properties and extensive intracellular or surface marker profiling, comprise promising avenues for rapid advancements in the understanding of disease progression and diagnosis. As protocols for conducting such imaging experiments continue to improve, it is the intent of this study to provide and validate software for processing the large quantity of associated data in kind.\n\nResultsCytokit offers (i) an end-to-end, GPU-accelerated image processing pipeline; (ii) efficient input/output (I/O) strategies for operations specific to high dimensional microscopy; and (iii) an interactive user interface for cross filtering of spatial, graphical, expression, and morphological cell properties within the 100+ GB image datasets common to multiplexed immunofluorescence. Image processing operations supported in Cytokit are generally sourced from existing deep learning models or are at least in part adapted from open source packages to run in a single or multi-GPU environment. The efficacy of these operations is demonstrated through several imaging experiments that pair Cytokit results with those from an independent but comparable assay. A further validation also demonstrates that previously published results can be reproduced from a publicly available multiplexed image dataset.\n\nConclusionCytokit is a collection of open source tools for quantifying and analyzing properties of individual cells in large fluorescent microscopy datasets that are often, but not necessarily, generated from multiplexed antibody labeling protocols over many fields of view or time periods. This project is best suited to bioinformaticians or other technical users that wish to analyze such data in a batch-oriented, high-throughput setting. All source code, documentation, and data generated for this article are available under the Apache License 2.0 at https://github.com/hammerlab/cytokit.

bioinformatics↗