arvkevi / clinvar-kaggleLinks
Scripts used to generate the ClinVar conflicting classifications dataset on Kaggle
☆15Updated 4 years ago
Alternatives and similar repositories for clinvar-kaggle
Users that are interested in clinvar-kaggle are comparing it to the libraries listed below
Sorting:
- Implementation of LSTM for detecting regions of Neanderthal introgression in modern human genomes☆9Updated 5 years ago
- Here I show how to use Deep Learning for biological and biomedical Data Integration.☆11Updated 4 years ago
- Applied Statistics for High-Throughput Biology☆16Updated 10 months ago
- Sequence data label generation and ingestion into deep learning models☆12Updated 3 years ago
- This repository contains all the source files required to run DeLUCS, a deep learning clustering algorithm for DNA sequences.☆25Updated 2 years ago
- GECO (Gene Expression Clustering Optimization; theGECOapp.com) is a minimalistic GUI app that utilizes non-linear reduction techniques to…☆9Updated last year
- Github Repository for multiOmics Integration project involving genomics, epigenomics and transcriptomics☆12Updated 4 years ago
- Deep learning methods for feature selection in gene expression autism data.☆36Updated 3 years ago
- End-to-End learning framework for circular RNA classification from other long non-coding RNA using multimodal deep learning☆24Updated 5 years ago
- Multifactorial modeling of response to checkpoint inhibitor immunotherapy from tumor, immune, and clinical features☆14Updated 6 years ago
- Large-scale automatic feature selection for biomarker discovery in high-dimensional OMICs data☆30Updated last year
- Main codes for AD epigenetics paper by Nativio et al.☆11Updated 5 years ago
- DSDE Deep Learning Club☆40Updated 6 years ago
- mRNN is an implementation of a Gated Recurrent Unit (GRU) network for classification of transcripts as either coding or noncoding.☆21Updated 6 years ago
- GenoML (genoml2) is an open source Python package. It is an automated machine learning (autoML) platform for genomics data☆32Updated last week
- Jupyter notebook for the application of convolutional neural nets to toy DNA sequence data☆15Updated 3 years ago
- BioBombe: Sequentially compressed gene expression features enhances biological signatures☆65Updated 11 months ago
- TeraPCA is a multithreaded C++ software suite based on Intel's MKL library (or any other BLAS and/or LAPACK distribution). TeraPCA featur…☆15Updated 2 years ago
- Coursera MOOC Algorithms for DNA Sequencing by Ben Langmead, PhD, Jacob Pritt☆13Updated 9 years ago
- iDeep: integrated prediction of RNA-protein binding sites using deep learning☆39Updated 4 years ago
- Data Integration tool utilizing network information for predictive analyses☆16Updated last month
- deep learning toolkit (written on top of tensorflow) to streamline computational biology analysis☆23Updated 2 years ago
- CNN based classifier for detecting viral sequences among metagenomic contigs☆33Updated 4 years ago
- jupyter notebook; perform differential gene expression analysis using DESeq2 on TCGA RNAseq data☆32Updated 6 years ago
- MOVIS: A Multi-Omics Software Solution for Multi-modal Time-Series Clustering, Embedding, and Visualizing Tasks, by Aleksandar Anžel, Dom…☆10Updated 3 years ago
- Find bimodal, unimodal, and multimodal features in your data☆27Updated 6 years ago
- Getting started guide to using GPUs for nCoV2019 research☆14Updated 5 years ago
- The Pathway Interaction Database (PID) is software supporting the access and display of information about bio-molecular interactions and …☆15Updated 9 years ago
- DeepNovo workflow of neoantigen discovery by personalized de novo sequencing.☆12Updated 4 years ago
- Ultrafast consensus module for raw de novo genome assembly of long uncorrected reads☆17Updated 4 years ago