interactive variant tables for easy filtering
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Updated
Jun 24, 2021 - R
interactive variant tables for easy filtering
Master's Thesis Project
An explorative tool to identify functional hotspots
Transcriptional variant verification to validate predicted variants from genomic data in expressed transcripts
Experimenting with protein language model predictions
Implementation of evolutionary model of variant effect (EVE), a deep generative model of evolutionary data, in PyTorch.
A Haskell script that performs basic parsing on the default output of ensembl-vep and variant-calling format (vcf) files.
Preliminary analysis of a combined DMS dataset, including clustering and VEP benchmark
Deep learning model for non-coding regulatory variants
Deep learning framework to predict functional effects of missense variants in human
Pipeline for variant annotation using Variant Effect Predictor (VEP)
Implementation of SpliceAI, Illumina's deep neural network to predict variant effects on splicing, in PyTorch.
CADD-SV – a framework to score the effect of structural variants
We present Envision, an accurate predictor of protein variant molecular effect, trained using large-scale experimental mutagenesis data. All data and software in this study are freely available. The training data set and all code used to train the models and generate the figures presented in this manuscript are available here. Envision predictio…
Clinical Whole Genome and Exome Sequencing Pipeline
Predicting the effect of mutations on protein stability and protein binding affinity using pretrained neural networks and a ranking objective function.
Fully convolutional deep learning variant effect predictor architecture
Tissue-specific variant effect predictions on splicing
Genomic Pre-trained Network
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