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jkanche authored Jul 22, 2024
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13 changes: 6 additions & 7 deletions howto.qmd
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Then checkout the [notebook](https://github.com/BiocPy/BiocWorkshop2024/tree/master/notebook) directory that contain Jupyter notebooks.

## Option 2: Using Google colab
## Option 2: Using Google Colab

To open the session in Google colab
To open the session in Google Colab:

1. Open [Google colab](https://colab.research.google.com/) in a new tab.
2. On the page, It should open up a dialog to "Open notebook" as shown in the screenshot below. If not, go to file -> Open Notebook from the menu in the top left.
2. On the page, it should open up a dialog to "Open notebook" as shown in the screenshot below.
* If no dialog appears, go to File -> Open Notebook from the menu (in the top left).
3. Choose Github and enter the repository url for the workshop: `https://github.com/BiocPy/BiocWorkshop2024`. This will automatically find the python notebooks available in the repository.

![](./assets/colab_session.png)
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![](./assets/colab_open_notebook.png)

:::{.callout-important}
This process does not download the [RDS file](https://github.com/BiocPy/BiocWorkshop2024/tree/master/notebook) available in the repository. Folks might have to manually download this to their colab sessions.
:::

and thats it!
This process does not download the [RDS file](https://github.com/BiocPy/BiocWorkshop2024/tree/master/notebook) available in the repository. Folks might have to manually download this to their Google Colab sessions.
:::
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## Welcome

Welcome to our workshop on exploring the data structures and packages
Welcome to our workshop on exploring the data structures and methods
available in [BiocPy](https://github.com/biocpy), a project that aims
to facilitate Bioconductor workflows in Python.

In this workshop, we will focus on interoperability between R and Python, covering two main topics:

- Reading an RDS file containing `GenomicRanges` and performing downstream range-based analyses.
- Annotating single-cell RNA-seq data using the [scrnaseq](https://github.com/biocpy/scrnaseq) package.
- Perform range-based analyses using [GenomicRanges](https://github.com/BiocPy/GenomicRanges).
- Annotate cell types in single-cell RNA-seq data stored as [SingleCellExperiment](https://github.com/BiocPy/SingleCellExperiment) object.

Attendees will learn how to represent and manipulate their datasets in Python
in the same manner as in R/Bioconductor.
All packages in BiocPy are published to PyPI, and the code is open-source
on [GitHub](https://github.com/BiocPy).

![](./assets/workshop.png)
<!-- ![](./assets/workshop.png) -->

### Core contributors
## Core contributors

- [Jayaram Kancherla](https://github.com/jkanche)
- [Aaron Lun](https://github.com/LTLA)
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## Developer notes

This is a reproducible Quarto book with reusable snippets. Check out [sessioninfo](./tutorials/sessioninfo.qmd) for packages installed during the build.
This is a reproducible Quarto book with reusable snippets. Check out the [session information](./tutorials/sessioninfo.qmd) for versions of installed packages.
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