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layout, title, description
| layout | title | description |
|---|---|---|
| default | FAQ | Frequently Asked Questions |
Data formatting
What file formats can I use with cellxgene?
Currently, you can go straight into cellxgene launch with your own analyzed data in h5ad format, after you have performed dimenstionality reduction (tsne, umap) and clustering (louvain).
If your data is in a different format, and/or you still need to perform dimensionality reduction and clustering, cellxgene can do that for you with the prepare command. cellxgene prepare runs scanpy under the hood and can read in any format that is currently supported by scanpy (including mtx, loom, and more listed here).
The output of cellxgene prepare is a h5ad file with your computed clusters and tsne/umap projections that can be used in cellxgene launch.
I have a directory of 10X-Genomics data with mtx files and I've never used scanpy, can I use cellxgene?
Yep! This should only take a couple steps. We'll assume your data is in a folder called data/ and you've successfully installed cellxgene with the louvain packages as described above. Just run
cellxgene prepare data/ --output=data-processed.h5ad --layout=umap
Depending on the size of the dataset, this may take some time. Once it's done, call
cellxgene launch data-processed.h5ad --layout=umap --open
And your web browser should open with an interactive view of your data.
I have extra metadata that I want to add to my dataset
Currently this is not supported directly, but you should be able to do this yourself using scanpy. For example, this notebook shows adding the contents of a csv file with metadata to an anndata object. For now, you could do this manually on your data in the same way and then save out the result before loading into cellxgene.
What part of the anndata objects does cellxgene pull in for visualization?
.obsand.varannotations are use to extract metadata for filtering.Xis used to display expression (histograms, scatterplot & colorscale) and to compute differential expression.obsmis used for layout
Algorithms
How are you computing and sorting differential expression results?
We use a Welch's t-test implementation including the same variance overestimation correction as used in scanpy. We sort the tscore to identify the top N genes, and then filter to remove any that fall below a cutoff log fold change value, which can help remove spurious test results. The default threshold is 0.01 and can be changed using the option --diffexp-lfc-cutoff.
Problems, errors, & bugs
How do I create a Python 3.6 environment for cellxgene?
If you use conda and want to create a conda environment for cellxgene you can use the following commands
conda create --yes -n cellxgene python=3.6
conda activate cellxgene
pip install cellxgene
Or you can create a virtual environment by using
ENV_NAME=cellxgene
python3.6 -m venv ${ENV_NAME}
source ${ENV_NAME}/bin/activate
pip install cellxgene
In my prepare command I received the following error Warning: louvain module is not installed, no clusters will be calculated. To fix this please install cellxgene with the optional feature louvain enabled
Louvain clustering requires additional dependencies, so we don't include them by default. For now, you need to specify that you want these packages by using
pip install cellxgene[louvain]
I ran prepare and I'm getting results that look unexpected
You might want to try running one of the preprocessing recipes included with scanpy (read more about them here). You can specify this with the --recipe option, such as
cellxgene prepare data/ --output=data-processed.h5ad --recipe=zheng17
It should be easy to run prepare then call cellxgene launch a few times with different settings to explore different behaviors. We may explore adding other preprocessing options in the future.
I tried to pip install cellxgene and got a weird error I don't understand
This may happen, especially as we work out bugs in our installation process! Please create a new Github issue, explain what you did, and include all the error messages you saw. It'd also be super helpful if you call pip freeze and include the full output alongside your issue.
I'm following the developer instructions and get an error about "missing files and directories” when trying to build the client
This is likely because you do not have node and npm installed, we recommend using nvm if you're new to using these tools.