Open wjddyd66 opened 3 years ago
HI @wjddyd66 , I am not sure what is going on, but please update to MOFA2 (https://github.com/bioFAM/MOFA2), as stated in the README file. The second version is much improved and this repository is no longer mantained.
See the "Getting started vignette" for Python. In addition, we now have a downstream analysis package coded in Python (https://github.com/gtca/mofax). It is less comprehensive though than the R package
Regarding SNPs, they are unlikely to be succesful in MOFA. This is because the genome does not show display many sources of variation between the features, except for population structure and related variables. This is unlike the transcriptome, which works in the form of a large number of gene regulatory networks that can vary massively across cell states, tissues, etc.
My Dataset is Like this...
SNP![image](https://user-images.githubusercontent.com/37298751/94503365-3d545980-0241-11eb-9a7b-0411ac7b1b8e.png)
Gene Expression
![image](https://user-images.githubusercontent.com/37298751/94503383-4c3b0c00-0241-11eb-8eea-947350714bc4.png)
Other Dataset
![image](https://user-images.githubusercontent.com/37298751/94503403-5bba5500-0241-11eb-855e-b87d427e5a16.png)
I have two question to mofapy/run/python_template.py
First
When the above code is executed, the following result window appears.
Is this warning code to group each sample together with the same samples based on the Pandas Index?
Second
When the above code is executed, the following result window appears.
Which dimension should be matched?
For reference, in the case of other datasets (complete data, the number of samples is the same in all modalities), no error occurred.
In the case of Incomplete Data, what additional work should be done?