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Builds, tests, diagnoses, upgrades, deploys and verifies Power Apps component framework (PCF) code components for model-driven apps and Power Pages — field and dataset controls, standard and virtual (React) — from Microsoft-maintained templates and recipes pinned to a tested version matrix. Runs quality gates (manifest and host lint, source checks, lint, unit tests, production build), deploys with pac pcf push, verifies registration and form bindings, and guides Power Pages enablement, with guided setup for canvas apps. Use when the user wants to build, fix, upgrade, deploy or check a PCF control or code component, or asks why one fails to build, import, update or render. For a whole page use /model-apps:genpage; for a whole app use /model-apps:app-builder.

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Use when finished Scenario assets have to give something back: a caption for a dataset or alt text, a reusable style description, a verdict against a brief, a canny, depth, pose, or segmentation control map for the next model, or the asset itself found again by text, tags, or visual similarity and filed into a collection. Keywords: caption, describe, analyze, QA, control map, find similar, reverse image search, semantic search, tag, collection.

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Access Google Data Commons public datasets and statistics

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Query NCBI Gene Expression Omnibus for transcriptomics datasets

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Access NCI Imaging Data Commons for medical imaging datasets

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Fine-tunes LLMs and trains custom models using LoRA/QLoRA adapters, JSONL training datasets, hyperparameter configuration, RLHF, DPO, and model quantization.

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Use when the user has evaluation principles or a dataset but needs help choosing the right graders, designing evaluation metrics, creating LLM-as-judge prompts, combining multiple metrics into a composite score, or building an automated evaluation pipeline. Also use when the user mentions grader selection, metric design, judge prompt engineering, rubric design, evaluation pipeline code, or "how to evaluate [X] automatically." Outputs executable OpenJudge pipeline code.

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Arbitrator research tool for investor-State dispute settlement (ISDS). The tool can summarize arbitrators' experience, with deliverables grounded in primary documents; it can also help find arbitrators based on the issues faced in a particular case. Use when the user asks about an arbitrator ("tell me about arbitrator X", "X, Y and Z"), wants help choosing or shortlisting arbitrators for a case, or asks about appointments, dissents, issue track records (e.g. FET, expropriation), challenge risk, double-hatting, or tribunal composition. Profiles are grounded in the UNCTAD ISDS Navigator dataset plus targeted live lookups (ICSID); deep verification retrieves the actual decisions. Sibling of isds-research.

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Train a character/identity LoRA locally on FLUX.1-dev via the comfyui-mcp train_* tools (GPU Docker + ostris ai-toolkit). Use when the user wants to train a LoRA of a person/character from their photos on the local GPU. Covers dataset prep, launch, monitoring, and using the result in ComfyUI. For WAN/Z-Image training via the ai-toolkit UI see ai-toolkit-trainer.

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Train custom LoRAs with ostris AI-Toolkit. Covers WAN 2.2/2.1 (people, styles, video motion) and Z-Image (Turbo & Base, low-VRAM image LoRAs). Use when the user wants to train a WAN or Z-Image LoRA; covers local + RunPod setup, dataset prep, key params, and using the result in a ComfyUI workflow.

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Train a custom anime LoRA on the ANIMA base model with Citron's local Gradio trainer (kohya sd-scripts), <6GB VRAM, character/style LoRAs; covers setup, dataset prep, training params, and using the result in the anima-base workflow

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Method for scalable identification of spatially variable genes (SVGs) in spatially-resolved transcriptomics data. The method is based on nearest-neighbor Gaussian processes and uses the BRISC algorithm for model fitting and parameter estimation. Allows identification and ranking of SVGs with flexible length scales across a tissue slide or within spatial domains defined by covariates. Scales linearly with the number of spatial locations and can be applied to datasets containing thousands or more

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SimBu can be used to simulate bulk RNA-seq datasets with known cell type fractions. You can either use your own single-cell study for the simulation or the sfaira database. Different pre-defined simulation scenarios exist, as are options to run custom simulations. Additionally, expression values can be adapted by adding an mRNA bias, which produces more biologically relevant simulations.

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The package comprises a set of pretrained machine learning models to predict basic immune cell types. This enables all users to quickly get a first annotation of the cell types present in their dataset without requiring prior knowledge. scAnnotatR also allows users to train their own models to predict new cell types based on specific research needs.

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Performs unbiased cell type recognition from single-cell RNA sequencing data, by leveraging reference transcriptomic datasets of pure cell types to infer the cell of origin of each single cell independently.

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performing all the steps of gene expression meta-analysis considering the possible existence of missing genes. It provides the necessary functions to be able to perform the different methods of gene expression meta-analysis. In addition, it contains functions to apply quality controls, download GEO datasets and show graphical representations of the results.

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Implements a variety of methods for combining p-values in differential analyses of genome-scale datasets. Functions can combine p-values across different tests in the same analysis (e.g., genomic windows in ChIP-seq, exons in RNA-seq) or fo

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This package encapsulate many functions to conduct a differential topology analysis. It focuses on analyzing an 'omic dataset with multiple conditions. While the package is mostly geared toward scRNASeq, it does not place any restriction on the actual input format.

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Dino normalizes single-cell, mRNA sequencing data to correct for technical variation, particularly sequencing depth, prior to downstream analysis. The approach produces a matrix of corrected expression for which the dependency between sequencing depth and the full distribution of normalized expression; many existing methods aim to remove only the dependency between sequencing depth and the mean of the normalized expression. This is particuarly useful in the context of highly sparse datasets such

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Fit linear models to overdispersed count data. The package can estimate the overdispersion and fit repeated models for matrix input. It is designed to handle large input datasets as they typically occur in single cell RNA-seq experiments.

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MEM, Marker Enrichment Modeling, automatically generates and displays quantitative labels for cell populations that have been identified from single-cell data. The input for MEM is a dataset that has pre-clustered or pre-gated populations with cells in rows and features in columns. Labels convey a list of measured features and the features' levels of relative enrichment on each population. MEM can be applied to a wide variety of data types and can compare between MEM labels from flow cytometry,

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HiContacts provides a collection of tools to analyse and visualize Hi-C datasets imported in R by HiCExperiment.

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Curated trending across GitHub repos and the Hugging Face Hub (models, datasets, spaces) - filtered, clustered, and labeled by momentum with a one-line why-notable per pick.

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Reverse-engineer raw materials (Sparse idea, Dense idea, experimental log) from an existing AI research paper to build a benchmark case for evaluating paper-writing pipelines. Replicates the PaperWritingBench dataset construction procedure from arXiv:2604.05018 §3 / App. C. TRIGGER when the user asks to "build a benchmark case from this paper", "reverse-engineer raw materials", or "evaluate my pipeline against PaperWritingBench".

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