Closed chrisprobert closed 7 years ago
Closed with #13. Thanks a ton @chrisprobert for the suggestion! I have included your name + a citation to this issue in the proposal. Please let me know by Sunday if you would prefer that I remove it.
A recent arxiv paper describes this idea, with code implemented in tensorflow here.
Note, the model is evaluated with 720 genes
Looks awesome!
On Fri, Sep 8, 2017 at 12:58 PM Greg Way notifications@github.com wrote:
A recent arxiv paper https://arxiv.org/abs/1709.02082 describes this idea, with code implemented in tensorflow here https://github.com/YosefLab/ZINB-VAE.
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Single-cell RNA-seq data is sparse/zero-inflated. There are several works [1-3] showing advantages of modeling zero-inflated distances between cells over L-1/L-2 distances.
For the VAE in aim 1, I expect that using zero inflated loss rather than euclidean reconstruction loss would work significantly better.
[1] https://genomebiology.biomedcentral.com/articles/10.1186/s13059-015-0805-z [2] https://arxiv.org/abs/1610.05857 [3] https://genomebiology.biomedcentral.com/articles/10.1186/s13059-017-1188-0