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update language to roadmap and a few other tweaks (#11)
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content/about/_index.md

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@@ -27,6 +27,7 @@ In 2016, members of this community co-founded the [CytoData Society](https://www
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The following year, the team contributed the landmark [Caicedo et al. 2017](https://doi.org/10.1038/nmeth.4397) review in _Nature Methods_ that established the field's foundational analysis standards.
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Since 2021, the [Way Lab](https://www.waysciencelab.com/) has driven a major expansion of the ecosystem — migrating from R to Python with `Pycytominer` and building a modern infrastructure stack including `CytoTable` and `coSMicQC`.
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In 2026, members of the CytoData community published an updated review, [Serrano et al.](https://doi.org/10.1038/s44320-026-00197-7) in _Molecular Systems Biology_, surveying progress and new challenges in image-based profiling.
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Today, Cytomining tools are used by research groups worldwide for drug discovery, functional genomics, and cell biology.
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## Community

content/experimental/_index.md

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---
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title: "Experimental"
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description: "Next-generation tools under active development in the WayScience organization."
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description: "Tools under active development in the WayScience organization, forming the foundation of the next Cytomining ecosystem."
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---
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The following tools are under active development in the [WayScience](https://github.com/WayScience) organization and represent the next generation of the Cytomining ecosystem.
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The following tools are under active development in the [WayScience](https://github.com/WayScience) organization and form the backbone of the Cytomining roadmap.

content/experimental/buscar.md

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title: "buscar"
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description: "Hit calling — identifies biologically active perturbations from single-cell morphological profiles using distribution-level scoring."
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description: "Hit calling — identifies biologically active perturbations from single-cell morphology profiles using distribution-level scoring."
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problem: "Population-level hit calling averages away cell-to-cell variation, hiding heterogeneous responses and rare subpopulations."
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showDate: false
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showAuthor: false

content/tools/copairs.md

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showAuthor: false
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`copairs` is a Python package for evaluating the quality of morphological profiles by measuring how well a perturbation's profile can be retrieved relative to controls.
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`copairs` is a Python package for evaluating the quality of morphology profiles by measuring how well a perturbation's profile can be retrieved relative to controls.
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It implements mean Average Precision (mAP) and related metrics widely used in the image-based profiling community.
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**Key capabilities:**

content/tools/cytodataframe.md

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title: "CytoDataFrame"
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description: "Interactive exploration — view and inspect morphological profiles alongside their source cell images directly in Jupyter notebooks."
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description: "Interactive exploration — view and inspect morphology profiles alongside their source cell images directly in Jupyter notebooks."
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showDate: false
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logoUrl: "https://raw.githubusercontent.com/cytomining/CytoDataFrame/main/logo/just-icon.png"
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<img class="logo-light" src="https://raw.githubusercontent.com/cytomining/CytoDataFrame/main/logo/with-text-for-light-bg.png" alt="CytoDataFrame logo" width="400">
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<img class="logo-dark" src="https://raw.githubusercontent.com/cytomining/CytoDataFrame/main/logo/with-text-for-dark-bg.png" alt="CytoDataFrame logo" width="400">
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`CytoDataFrame` extends the familiar pandas DataFrame interface to let researchers view and analyze single-cell morphological profiles alongside their corresponding microscopy images and segmentation masks — all within a Jupyter notebook.
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`CytoDataFrame` extends the familiar pandas DataFrame interface to let researchers view and analyze single-cell morphology profiles alongside their corresponding microscopy images and segmentation masks — all within a Jupyter notebook.
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**Key capabilities:**
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content/tools/cytotable.md

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<img class="logo-dark" src="https://raw.githubusercontent.com/cytomining/CytoTable/main/logo/with-text-for-dark-bg.png" alt="CytoTable logo" width="400">
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`CytoTable` harmonizes output from different high-content image analysis tools — including CellProfiler, `DeepProfiler`, and IN Carta — into a single, analysis-ready format.
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It scales to large datasets using Apache Parquet and DuckDB under the hood.
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It scales to large datasets using Apache Parquet, DuckDB, and Parsl under the hood.
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**Key capabilities:**
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content/tools/pycytominer.md

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title: "Pycytominer"
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description: "Core processing pipeline — aggregates, normalizes, and feature-selects morphological profiles for downstream analysis."
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description: "Core processing pipeline — aggregates, normalizes, and feature-selects morphology profiles for downstream analysis."
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showDate: false
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logoUrl: "https://raw.githubusercontent.com/cytomining/pycytominer/main/logo/just-icon.png"
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<img class="logo-dark" src="https://raw.githubusercontent.com/cytomining/pycytominer/main/logo/with-text-for-dark-bg.png" alt="Pycytominer logo" width="400">
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`Pycytominer` is the core Python package in the Cytomining ecosystem.
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It provides a clean, composable API for processing single-cell morphological profiles produced by tools like CellProfiler.
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It provides a clean, composable API for processing single-cell morphology profiles produced by tools like CellProfiler.
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**Key capabilities:**
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layouts/experimental/list.html

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<h1 class="hero-fade-1 text-4xl font-extrabold mb-2">Experimental Tools</h1>
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<p class="hero-fade-2" style="color: #6b7280; font-size: 1.05rem; margin-bottom: 2.5rem; line-height: 1.65;">
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Next-generation tools under active development in the <a href="https://github.com/WayScience" style="color: inherit; text-decoration: underline; text-decoration-color: #d1d5db;">WayScience</a> organization,
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designed to become the foundation of Cytomining v2.
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forming the foundation of the Cytomining roadmap.
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</p>
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{{/* V2 pitch */}}
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{{/* Roadmap pitch */}}
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<div class="hero-fade-3 v2-callout" style="border-left: 3px solid #2563eb; padding: 1rem 1.25rem; background: #eff6ff; border-radius: 0 8px 8px 0; margin-bottom: 2rem;">
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<p style="font-weight: 700; font-size: 1rem; margin: 0 0 0.5rem; color: #1e40af;">What does Cytomining v2 solve?</p>
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<p style="font-weight: 700; font-size: 1rem; margin: 0 0 0.5rem; color: #1e40af;">What gaps does our roadmap address?</p>
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<p style="margin: 0; font-size: 0.92rem; color: #1e3a5f; line-height: 1.65;">
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The current Cytomining stack was designed around 2D single-cell data from CellProfiler.
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As the field moves toward <strong>3D organoid imaging</strong>, <strong>larger-scale archives</strong>, and <strong>deep learning feature extraction</strong>,
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several gaps have emerged: no standardized image catalog, images and features stored separately, no 3D support, and hit calling that collapses single-cell heterogeneity.
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The tools below are purpose-built to close each of these gaps — together forming a fully traceable, format-agnostic, 3D-capable profiling pipeline.
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As the field moves toward <strong>3D organoid imaging</strong>, <strong>single-cell profiling</strong>, <strong>larger-scale screens</strong>, and <strong>deep learning feature extraction</strong>,
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several gaps have emerged: no standardized image catalog, images and features stored separately, limited 3D support, and hit calling that collapses single-cell heterogeneity.
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We are building the tools below to close each of these gaps and raise the computational pipeline to support the demands of data collection and goals of the moment.
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</p>
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</div>
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</div>
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{{/* V2 pipelines */}}
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<h2 class="hero-fade-5" style="font-size: 1.15rem; font-weight: 700; margin-top: 3rem; margin-bottom: 1.25rem;">Cytomining v2 pipelines</h2>
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<h2 class="hero-fade-5" style="font-size: 1.15rem; font-weight: 700; margin-top: 3rem; margin-bottom: 1.25rem;">Roadmap pipelines</h2>
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{{/* Pipeline 1: standard (2D) */}}
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<div class="hero-fade-6" style="margin-bottom: 1.5rem;">

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