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predicting expression effects of human genome variants ab initio from sequence

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Hi, thanks for the great tool! I notice that expecto takes a sequence around TSS to predict the tissue-specific expression values and calculate the expression difference between ref and alt...

How does Beluga handle sequences < 1,000bp? Does it center on the input sequence and pad it with N's, or does it do something else? Thanks!

Hi, Could you provide the python script to produce Xreducedall.2002.npy file, pls? Maybe we can use the pipeline for another organisms analysis, such as FLY. Thansk in advance!!! Best Wishes,

For other purposes I wanted to get a single chromatin effect score for each SNP from what I can tell if X = num_variants then for each SNP i then...

I'm interested in the method to get the representative TSS site you provided in "Deep learning sequence-based ab initio prediction of variant effects on expression and disease risk". In the...

Hi, I used the script "predict.py" to do the prediction of a vcf file, and I find that there is some difference between these results and the results from ExPecto...

Hi, I want to get 2002 narrow-peak files of matin features, but I did not provide the link in the file "deepsea_beluga_2002_features.tsv". I can only download 874 of them through...

I am running this program on a shared cluster and using data for ~1,000 variant mutations worked within the constraints of system/memory usage for jobs on this cluster; however, trying...

Hello, I'm trying to replicate the features in `resources/Xreducedall.2002.npy`. I am able to get within 99% spearman correlation, but I'm not able to replicate the features exactly. Would you be...

Thank you for making your code and model available! I just wanted to bring it to your attention that there appears to be a discrepancy between the architecture specified in...