Trajectory Analysis using Python (Jupyter Notebook) in Galaxy


question Questions
  • How can I infer lineage relationships between single cells based on their RNA, without a time series?

objectives Objectives
  • Execute multiple plotting methods designed to maintain lineage relationships between cells

  • Interpret these plots

requirements Requirements

time Time estimation: 2 hours

Supporting Materials

last_modification Last modification: Apr 29, 2021


You’ve done all the hard work of preparing a single cell matrix, processing it, plotting it, interpreting it, finding lots of lovely genes, all within the glorious Galaxy interface. Now you want to infer trajectories, or relationships between cells… and you’ve been threatened with learning Python to do so! Well, fear not. If you can have a run-through of a basic python coding introduction such as this one, then that will help you make more sense of this tutorial, however you’ll be able to make and interpret glorious plots even without understanding the Python coding language. This is the beauty of Galaxy - all the ‘set-up’ is identical across computers, because it’s browser based. So fear not!

Traditionally, we thought that differentiating or changing cells jumped between discrete states, so ‘Cell A’ became ‘Cell B’ as part of its maturation. However, most data shows otherwise, that generally there is a spectrum (a ‘trajectory’, if you will…) of small, subtle changes along a pathway of that differentiation. Trying to analyse cells every 10 seconds can be pretty tricky, so ‘pseudotime’ analysis takes a single sample and assumes that those cells are all on slightly different points along a path of differentiation. Some cells might be slightly more mature and others slightly less, all captured at the same ‘time’. We ‘assume’ or ‘infer’ relationships between cells.

We will use the same sample from the previous two tutorials, which contains largely T-cells in the thymus. We know T-cells differentiate in the thymus, so we would assume that we would capture cells at slightly different time points within the same sample. Furthermore, our cluster analysis alone showed different states of T-cell. Now it’s time to look further!


In this tutorial, we will cover:

  1. Get data
  2. Filtering for T-cells
  3. Launching Jupyter
  4. Run the tutorial!
  5. Tutorial Plot Answers
  6. After Jupyter

Get data

We’ve provided you with experimental data to analyse from a mouse dataset of fetal growth restriction Bacon et al. 2018. This is the full dataset generated from this tutorial (see the study in Single Cell Expression Atlas here and the project submission here). You can find the final dataset in this input history or download from Zenodo below.

hands_on Hands-on: Data upload

  1. Create a new history for this tutorial
  2. Import the AnnData object from Zenodo
    • Copy the link location
    • Open the Galaxy Upload Manager (galaxy-upload on the top-right of the tool panel)
    • Select Paste/Fetch Data
    • Paste the link into the text field
    • Press Start
    • Close the windowBy default, Galaxy uses the URL as the name, so rename the files with a more useful name.
  3. Rename galaxy-pencil the .h5ad object as Final cell annotated object

    Tip: Renaming a dataset

    • Click on the galaxy-pencil pencil icon for the dataset to edit its attributes
    • In the central panel, change the Name field to Final cell annotated object
    • Click the Save button
  4. Check that the datatype is h5ad

    Tip: Changing the datatype

    • Click on the galaxy-pencil pencil icon for the dataset to edit its attributes
    • In the central panel, click on the galaxy-chart-select-data Datatypes tab on the top
    • Select h5ad
    • Click the Change datatype button
  5. Rename galaxy-pencil the .ipynb object as Trajectories_Instructions.ipynb

  6. Check that the datatype is .ipynb

Filtering for T-cells

One problem with our current dataset is that it’s not just T-cells: we found in the previous tutorial that it also contains macrophages and red blood cells. This is a problem, because trajectory analysis will generally try to find relationships between all the cells in the sample. We need to remove those cell types to analyse the trajectory.

hands_on Hands-on: Removing macrophages and RBCs

  1. Manipulate AnnData Tool: with the following parameters:
    • param-file “Annotated data matrix”: Final cell annotated object
    • “Function to manipulate the object”: Filter observations or variables
    • “What to filter?”: Observations (obs)
    • “Type of filtering?”: By key (column) values
    • “Key to filter”: cell_type
    • “Type of value to filter”: Text
    • “Filter”: not equal to
    • “Value”: RBC
  2. Manipulate AnnData Tool: with the following parameters:
    • param-file “Annotated data matrix”: (output of Manipulate AnnData tool)
    • “Function to manipulate the object”: Filter observations or variables
    • “What to filter?”: Observations (obs)
    • “Type of filtering?”: By key (column) values
    • “Key to filter”: cell_type
    • “Type of value to filter”: Text
    • “Filter”: not equal to
    • “Value”: Macrophages
  3. Rename galaxy-pencil output h5ad T-cell_object.h5ad

You should now have 7795 cells, as opposed to the 7874 you started with. You’ve only removed a few cells (the contaminants!), but it makes a big difference in the next steps.

Take note of what # this dataset is in your history, as you will need that shortly!

Launching Jupyter

hands_on Hands-on: Downloading the directions

  1. Click the Trajectories_Instructions.ipynb dataset and the download galaxy-save button to get the file onto your computer

JupyterLab is a bit like RStudio but for other coding languages. What, you’ve never heard of RStudio? Then don’t worry, just follow the instructions!

warning Please note: this is only currently available on the and sites.

hands_on Hands-on: Launching JupyterLab

  1. Interactive Jupyter Notebook Tool: interactive_tool_jupyter_notebook with the following parameters:
    • “Do you already have a notebook?”: Start with a fresh notebook
    • param-file “Include data into the environment”: Nothing selected

    This may take a moment, but once the Executed notebook in your dataset is orange, you are up and running!

  2. Either click on the blue User menu, or go to the top of the screen and choose User and then Active InteractiveTools

  3. Click on the newest Jupyter Interactive Tool.


warning Danger: You can lose data!

Do NOT delete or close this notebook dataset in your history. YOU WILL LOSE IT!

hands_on Hands-on: Creating a notebook

  1. Click the Python 3 icon under Notebook
Python 3 icon
Figure 1: Python 3 Button
  1. Save your file (File: Save, or click the galaxy-save Save icon at the top left)

  2. If you right click on the file in the folder window at the left, you can rename your file whateveryoulike.ipynb

Cool! Now you know how to create a file! Helpfully, however, we have created one for you, and you’ve downloaded it onto your computer already!

hands_on Hands-on: Uploading the tutorial notebook

  1. In the folder window, galaxy-upload Upload the Trajectories_Instructions.ipynb from your computer. It should appear in the file window.

  2. Open it by double clicking it in the file window.

warning You should galaxy-save Save frequently!

This is both for good practice and to protect you in case you accidentally close the browser. Your environment will still run, so it will contain the last saved notebook you have. You might eventually stop your environment after this tutorial, but ONLY once you have saved and exported your notebook (more on that at the end!) Note that you can have multiple notebooks going at the same time within this JupyterLab, so if you do, you will need to save and export each individual notebook. You can also download them at any time.

Run the tutorial!

At this point, to prevent you having to switch back and forth between browsers, the directions for the rest of tutorial are all in the notebook you input! Go to data and double click Trajectories_Instructions.ipynb You may have to change certain numbers in the code blocks, so do read carefully. You will be able to run each step be clicking on the code block and pressing the workflow-run Run the selected cells and advance step. You will want to keep a tab open with your Galaxy history showing (so just launch another browser of your instance), so that you can see when your files appear there. The tutorial is adapted from the Scanpy Trajectory inference tutorial.

Tutorial Plot Answers

Just in case, we’ve put the plots you should generate in the tutorial here. If things have gone wrong, you can also download this answer key tutorial.

Plot1-Force-Directed Graph
Figure 2: Plot1-Force-Directed Graph
Diffusion Map
Figure 3: Diffusion Map
Figure 4: PAGA
Force-Directed + PAGA - Cell type
Figure 5: Force-Directed + PAGA - Cell type
Force-Directed + PAGA - Genotype
Figure 6: Force-Directed + PAGA - Genotype
Force-Directed + PAGA - Markers
Figure 7: Force-Directed + PAGA - Markers
Force-Directed + Pseudotime
Figure 8: Force-Directed + Pseudotime

After Jupyter

congratulations Congratulations! You’ve made it through Jupyter!

hands_on Hands-on: Closing JupyterLab

  1. Click User: Active Interactive Tools

  2. Tick galaxy-selector the box of your Jupyter Interactive Tool, and click Stop

If you want to run this notebook again, or share it with others, it now exists in your history. You can use this ‘finished’ version just the same way as you downloaded the directions file and uploaded into the Jupyter environment.


congratulations Congratulations! You’ve made it to the end! You might be interested in the Answer Key History

In this tutorial, you moved from called clusters to inferred relationships and trajectories using pseudotime analysis. You found an alternative to PCA (diffusion map), an alternative to tSNE (force-directed graph), a means of identifying cluster relationships (PAGA), and a metric for pseudotime (diffusion pseudotime) to identify early and late cells. If you were working in a group, you found that such analysis is slightly more sensitive to your decisions than the simpler filtering/plotting/clustering is. We are inferring and assuming relationships and time, so that makes sense!

To discuss with like-minded scientists, join our Gitter channel for all things Galaxy-single cell! Gitter

keypoints Key points

  • Trajectory analysis is less robust than pure plotting methods, as such ‘inferred relationships’ are a bigger mathematical leap

  • As always with single-cell analysis, you must know enough biology to deduce if your analysis is reasonable, before exploring or deducing novel insight

Frequently Asked Questions

Have questions about this tutorial? Check out the FAQ page for the Transcriptomics topic to see if your question is listed there. If not, please ask your question on the GTN Gitter Channel or the Galaxy Help Forum

Useful literature

Further information, including links to documentation and original publications, regarding the tools, analysis techniques and the interpretation of results described in this tutorial can be found here.


  1. Bacon, W. A., R. S. Hamilton, Z. Yu, J. Kieckbusch, D. Hawkes et al., 2018 Single-Cell Analysis Identifies Thymic Maturation Delay in Growth-Restricted Neonatal Mice. Frontiers in Immunology 9: 10.3389/fimmu.2018.02523


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Citing this Tutorial

  1. Wendi Bacon, Mehmet Tekman, 2021 Trajectory Analysis using Python (Jupyter Notebook) in Galaxy (Galaxy Training Materials). /training-material/topics/transcriptomics/tutorials/scrna-JUPYTER-trajectories/tutorial.html Online; accessed TODAY
  2. Batut et al., 2018 Community-Driven Data Analysis Training for Biology Cell Systems 10.1016/j.cels.2018.05.012

details BibTeX

    author = "Wendi Bacon and Mehmet Tekman",
    title = "Trajectory Analysis using Python (Jupyter Notebook) in Galaxy (Galaxy Training Materials)",
    year = "2021",
    month = "04",
    day = "29"
    url = "\url{/training-material/topics/transcriptomics/tutorials/scrna-JUPYTER-trajectories/tutorial.html}",
    note = "[Online; accessed TODAY]"
        doi = {10.1016/j.cels.2018.05.012},
        url = {},
        year = 2018,
        month = {jun},
        publisher = {Elsevier {BV}},
        volume = {6},
        number = {6},
        pages = {752--758.e1},
        author = {B{\'{e}}r{\'{e}}nice Batut and Saskia Hiltemann and Andrea Bagnacani and Dannon Baker and Vivek Bhardwaj and Clemens Blank and Anthony Bretaudeau and Loraine Brillet-Gu{\'{e}}guen and Martin {\v{C}}ech and John Chilton and Dave Clements and Olivia Doppelt-Azeroual and Anika Erxleben and Mallory Ann Freeberg and Simon Gladman and Youri Hoogstrate and Hans-Rudolf Hotz and Torsten Houwaart and Pratik Jagtap and Delphine Larivi{\`{e}}re and Gildas Le Corguill{\'{e}} and Thomas Manke and Fabien Mareuil and Fidel Ram{\'{\i}}rez and Devon Ryan and Florian Christoph Sigloch and Nicola Soranzo and Joachim Wolff and Pavankumar Videm and Markus Wolfien and Aisanjiang Wubuli and Dilmurat Yusuf and James Taylor and Rolf Backofen and Anton Nekrutenko and Björn Grüning},
        title = {Community-Driven Data Analysis Training for Biology},
        journal = {Cell Systems}

congratulations Congratulations on successfully completing this tutorial!