<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Experimental on Cytomining</title><link>https://cytomining.github.io/experimental/</link><description>Recent content in Experimental on Cytomining</description><generator>Hugo</generator><language>en</language><atom:link href="https://cytomining.github.io/experimental/index.xml" rel="self" type="application/rss+xml"/><item><title>buscar</title><link>https://cytomining.github.io/experimental/buscar/</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://cytomining.github.io/experimental/buscar/</guid><description>&lt;img class="logo-light" src="https://raw.githubusercontent.com/WayScience/buscar/main/logo/with-text-for-light-bg.png" alt="buscar logo" width="400"&gt;
&lt;img class="logo-dark" src="https://raw.githubusercontent.com/WayScience/buscar/main/logo/with-text-for-dark-bg.png" alt="buscar logo" width="400"&gt;
&lt;p&gt;buscar is a Python package for reproducible hit calling in high-content screening.
Rather than averaging cells into population-level summaries, it operates on individual cell distributions to preserve biological heterogeneity and identify perturbations with on-target morphological signatures.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key capabilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Define on-target and off-target morphology signatures from reference profiles&lt;/li&gt;
&lt;li&gt;Score perturbation efficacy via Earth Mover&amp;rsquo;s Distance&lt;/li&gt;
&lt;li&gt;Assess specificity with off-target scoring to reduce false positives&lt;/li&gt;
&lt;li&gt;Preserve single-cell heterogeneity throughout hit calling&lt;/li&gt;
&lt;li&gt;Integrates directly with pycytominer, coSMicQC, and CytoTable workflows&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;a href="https://github.com/WayScience/buscar" target="_blank" rel="noreferrer"&gt;View on GitHub →&lt;/a&gt;&lt;/strong&gt;&lt;/p&gt;</description></item><item><title>iceberg-bioimage</title><link>https://cytomining.github.io/experimental/iceberg-bioimage/</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://cytomining.github.io/experimental/iceberg-bioimage/</guid><description>&lt;img src="https://raw.githubusercontent.com/WayScience/iceberg-bioimage/main/docs/src/_static/iceberg-bioimage-logo.png" alt="iceberg-bioimage logo" width="400"&gt;
&lt;p&gt;iceberg-bioimage is a Python package that catalogs bioimaging data using Apache Iceberg.
It scans image stores across formats, publishes structured metadata tables, and exports layouts compatible with the Cytomining profiling ecosystem — bridging raw image archives and downstream analysis pipelines.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key capabilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Scan image stores into canonical &lt;code&gt;ScanResult&lt;/code&gt; objects&lt;/li&gt;
&lt;li&gt;Publish image metadata with PyIceberg for versioned, queryable catalogs&lt;/li&gt;
&lt;li&gt;Export Cytomining-compatible Parquet warehouses for profiling workflows&lt;/li&gt;
&lt;li&gt;Validate profile tables against microscopy join contracts&lt;/li&gt;
&lt;li&gt;Supports Zarr, OME-TIFF, and Parquet source formats&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;a href="https://wayscience.github.io/iceberg-bioimage/" target="_blank" rel="noreferrer"&gt;View documentation →&lt;/a&gt;&lt;/strong&gt;&lt;/p&gt;</description></item><item><title>OME-arrow</title><link>https://cytomining.github.io/experimental/ome-arrow/</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://cytomining.github.io/experimental/ome-arrow/</guid><description>&lt;img src="https://raw.githubusercontent.com/WayScience/OME-arrow/main/docs/src/_static/ome-arrow-logo.png" alt="OME-arrow logo" width="400"&gt;
&lt;p&gt;OME-arrow brings Open Microscopy Environment (OME) specifications to Apache Arrow, enabling microscopy images to be stored directly in data tables alongside their metadata and derived features as multilayer structs.
This makes bioimaging data fast to query, easy to share, and compatible with modern tensor-based ML workflows.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key capabilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Store images, metadata, and derived features together in a single table&lt;/li&gt;
&lt;li&gt;Support for TIFF, OME-Zarr, NumPy, and Parquet source formats&lt;/li&gt;
&lt;li&gt;Lazy reading and region-of-interest (ROI) access for large datasets&lt;/li&gt;
&lt;li&gt;Tensor-focused output compatible with PyTorch, JAX, and DLPack&lt;/li&gt;
&lt;li&gt;Visualization integrations for matplotlib, PyVista, and Napari&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;a href="https://wayscience.github.io/ome-arrow/" target="_blank" rel="noreferrer"&gt;View documentation →&lt;/a&gt;&lt;/strong&gt;&lt;/p&gt;</description></item><item><title>zedprofiler</title><link>https://cytomining.github.io/experimental/zedprofiler/</link><pubDate>Mon, 01 Jan 0001 00:00:00 +0000</pubDate><guid>https://cytomining.github.io/experimental/zedprofiler/</guid><description>&lt;p&gt;zedprofiler is a CPU-first toolkit for extracting morphological features from 3D volumetric microscopy images.
It is designed for high-content and high-throughput workflows where classical segmentation-and-measurement pipelines need to scale to single-cell features in z-stacks.&lt;/p&gt;
&lt;p&gt;&lt;strong&gt;Key capabilities:&lt;/strong&gt;&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Extract features from 3D volumetric (z-stack) single-cell images&lt;/li&gt;
&lt;li&gt;Multi-channel fluorescence microscopy support&lt;/li&gt;
&lt;li&gt;Anisotropic voxel spacing correction for accurate 3D measurements&lt;/li&gt;
&lt;li&gt;Modular, extensible architecture for custom feature sets&lt;/li&gt;
&lt;li&gt;CPU-optimized for high-throughput processing without GPU dependency&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;&lt;strong&gt;&lt;a href="https://github.com/WayScience/zedprofiler" target="_blank" rel="noreferrer"&gt;View on GitHub →&lt;/a&gt;&lt;/strong&gt;&lt;/p&gt;</description></item></channel></rss>