Nucleoli Segmentation & Feature Extraction using CellProfiler

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# Nucleoli Segmentation <br> & <br> Feature Extraction <br> using CellProfiler

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  <a href="/training-material/hall-of-fame/beatrizserrano/" class="contributor-badge contributor-beatrizserrano"><img src="/training-material/assets/images/orcid.png" alt="orcid logo" width="36" height="36"/><img src="https://avatars.githubusercontent.com/beatrizserrano?s=36" alt="Beatriz Serrano-Solano avatar" width="36" class="avatar" />
    Beatriz Serrano-Solano</a>
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## Requirements

Before diving into this slide deck, we recommend you to have a look at:

- [Introduction to Galaxy Analyses](/training-material/topics/introduction)

- [FAIR Data, Workflows, and Research](/training-material/topics/fair)
    - FAIR Bioimage Metadata: [<i class="fas fa-laptop" aria-hidden="true"></i><span class="visually-hidden">tutorial</span> hands-on](/training-material/topics/fair/tutorials/bioimage-metadata/tutorial.html)
    - REMBI - Recommended Metadata for Biological Images – metadata guidelines for bioimaging data: [<i class="fas fa-laptop" aria-hidden="true"></i><span class="visually-hidden">tutorial</span> hands-on](/training-material/topics/fair/tutorials/bioimage-REMBI/tutorial.html)

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### <i class="far fa-question-circle" aria-hidden="true"></i><span class="visually-hidden">question</span> Questions

- How do I run an image analysis pipeline on public data using CellProfiler?

- How do I analyse the DNA channel of fluorescence siRNA screens?

- How do I download public image data into my history?

- How do I segment and label cell nuclei?

- How do I segment nucleoli (as the absence of DNA)?

- How do I combine nuclei and nucleoli into one segmentation mask?

- How do I extract the background of an image?

- How do I relate the nucleoli to their parent nucleus?

- How do I measure the image and object features?

- How do I measure the image quality?

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### <i class="fas fa-bullseye" aria-hidden="true"></i><span class="visually-hidden">objectives</span> Objectives

- How to download images from a public image repository.

- How to segment cell nuclei using CellProfiler in Galaxy.

- How to segment cell nucleoli using CellProfiler in Galaxy.

- How to extract features for images, nuclei and nucleoli.

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### What is the nucleoli?

- Membrane-less organelle in the nucleus of the cell
- Functions: ribosome biogenesis and cell cycle regulation

.image-55[
  ![image of four cells, one is dividing, and red arrows point to the 5 nucleii](../../images/tutorial-CP/img_dna_channel.png)
]

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In the DNA channel, the nucleoli is shown as the absence of DNA (red arrows).
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### Data

- The data can be downloaded from the Image Data Resource ([IDR](http://idr.openmicroscopy.org/))

.image-65[
  ![screenshot of a complex tool interface showing an array of images (1) and then two selected images below it (2) and a configuration panel on the right (3)](../../images/tutorial-CP/IDR_interface.jpg)
]

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In the IDR the images can be selected in the user interface (1). The images will then show up at the bottom (2) where they need to be selected once again and then copy the URL from the link icon on the top left (3). That URL contains the image ids that will be downloaded.
You can also bring your images by uploading the DNA channel of your images to your Galaxy history.
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### General Workflow

- The workflow contains 4 basic parts:
  - Segmentation of the nuclei
  - Segmentation of the nucleoli that fall inside the nuclei
  - Background detection
  - Feature extraction of the images and objects

![screenshot of a galaxy workflow with four sections highlighted by boxes reading nuclei, nucleoli, background, and feature extraction.](../../images/tutorial-CP/wf.jpg "High-level view of the workflow")

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- Segmentation of the nucleoli: since there is no staining for the nucleoli, the holes need to be detected and segmented.
- Feature extraction: the order of the tools does not affect the outcome.
- Background detection: Detection of the foreground and subtraction from the image.
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### 1) Segment nuclei

![Inset to the first portion of the above overview image showing nuclei with 5 steps, starting modules, segment complete nuclei, segmentation mask complete nuclei, label nuclei, and save labelled nuclei.](../../images/tutorial-CP/subwf_nuclei.jpg)

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Every CellProfiler pipeline needs to start by processing the metadata with the tool "Starting modules".

- Segment complete nuclei: this tool identifies the nuclei within a certain size and excludes those cells that are touching the borders of the image.
- Segmentation mask complete nuclei: gathers all the nuclei identified in the previous step in one mask.
- Label and save labelled nuclei: adds the id of each nucleus on top of it. This can be useful later for a proper interpretation of the data analysis.---

### Segmentation and labelling of the nuclei

![a photo of cells in black and white, several cells have red numbers written atop them.](../../images/tutorial-CP/img_nuclei_labels.png "Identified nuclei with labels")

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Resulting image after the first logical step of the workflow in which the nuclei were segmented and labelled.
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### 2) Segment nucleoli

![Inset of the nucleoli portion of the workflow with the following steps: detect dark holes in nuclei, segment nucleoli that fall inside nuclei, segment nucleoli, convert the segmented nucleoli into an image, combine masks (nuclei+nucleoli), and finally save combined segmentation masks.](../../images/tutorial-CP/subwf_nucleoli.jpg)

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To identify the nucleoli the first step is to enhance the dark holes so that they can be segmented.
The segmentation of the dark holes will take place only when the dark holes fall inside a nucleus. This is to avoid the detection of wrong objects outside the cell.
At this step, the segmentation of the nucleoli can be performed.
It will be useful for visual exploration that the masks of the nuclei and nucleoli are saved together into one segmentation mask.
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### Combined mask: nuclei + nucleoli

![image of the cells again, but now cells are blue and nuclei/nucleoli are red.](../../images/tutorial-CP/img_combined_masks.png "Nuclei and nucleoli masks combined in which the nuclei are in blue and nucleoli in magenta.")

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The combination of both masks gives an image with the nuclei in blue and the nucleoli in magenta.
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### Background extraction

![third inset workflow, background extraction, with steps segment all nuclei, segmentation mask nucleoli including cells touching borders, and extract background.](../../images/tutorial-CP/subwf_background.jpg)

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The extraction of the background can be useful to measure features that indicate that the images are artefacts.
To get the background we first select the foreground and subtract it from the original image.
We have partially detected the foreground in the nuclei segmentation in previous steps. However, that mask only included just those objects within a max and a min pixel size. We also discarded the images touching the borders. Here, we get rid of the constraints and segment all the nuclei.

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### Feature extraction

![The final inset, feature extraction with very small steps.](../../images/tutorial-CP/subwf_feature_extraction.jpg)

- **Important:** Relate nucleoli and parent nucleus

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The features can be extracted from the images and the objects. Depending on which type of object and the interest of the study, different parameters can be measured.
The module that relates the objects is useful to export a table with the ids of the nucleoli in relation with their parent nuclei. That's useful for a meaningful interpretation of the data.

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### <i class="fas fa-key" aria-hidden="true"></i><span class="visually-hidden">keypoints</span> Key points

- Galaxy workflows can download images from the IDR, selecting specific channels, time points, z-stack positions and crop the image in different ways.

- CellProfiler in Galaxy can segment and extract features of any object of interest.

- The features and masks can be exported for further analysis.

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## Thank You!

This material is the result of a collaborative work. Thanks to the [Galaxy Training Network](https://training.galaxyproject.org) and all the contributors!

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		<td><abbr title="These people wrote the bulk of the tutorial, they may have done the analysis, built the workflow, and wrote the text themselves.">Author(s)</abbr></td>
		<td>
			
  <a href="/training-material/hall-of-fame/beatrizserrano/" class="contributor-badge contributor-beatrizserrano"><img src="/training-material/assets/images/orcid.png" alt="orcid logo" width="36" height="36"/><img src="https://avatars.githubusercontent.com/beatrizserrano?s=36" alt="Beatriz Serrano-Solano avatar" width="36" class="avatar" />
    Beatriz Serrano-Solano</a>
  
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  <a href="/training-material/hall-of-fame/bgruening/" class="contributor-badge contributor-bgruening">
    <img src="https://avatars.githubusercontent.com/bgruening?s=36" alt="Björn Grüning avatar" width="36" class="avatar" />
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  <a href="/training-material/hall-of-fame/beatrizserrano/" class="contributor-badge contributor-beatrizserrano">
    <img src="https://avatars.githubusercontent.com/beatrizserrano?s=36" alt="Beatriz Serrano-Solano avatar" width="36" class="avatar" />
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  <a href="/training-material/hall-of-fame/annefou/" class="contributor-badge contributor-annefou">
    <img src="https://avatars.githubusercontent.com/annefou?s=36" alt="Anne Fouilloux avatar" width="36" class="avatar" />
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  <a href="/training-material/hall-of-fame/shiltemann/" class="contributor-badge contributor-shiltemann">
    <img src="https://avatars.githubusercontent.com/shiltemann?s=36" alt="Saskia Hiltemann avatar" width="36" class="avatar" />
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  <a href="/training-material/hall-of-fame/gallardoalba/" class="contributor-badge contributor-gallardoalba">
    <img src="https://avatars.githubusercontent.com/gallardoalba?s=36" alt="Cristóbal Gallardo avatar" width="36" class="avatar" />
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Tutorial Content is licensed under <a rel="license" href="http://creativecommons.org/licenses/by/4.0/">Creative Commons Attribution 4.0 International License</a>.<br/>