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deeplift
Public facing deeplift repodragonn
A toolkit to learn how to model and interpret regulatory sequence data using deep learning.atac_dnase_pipelines
ATAC-seq and DNase-seq processing pipelinebpnet
Toolkit to train base-resolution deep neural networks on functional genomics data and to interpret themtfmodisco
TF MOtif Discovery from Importance SCOreschrombpnet
Bias factorized, base-resolution deep learning models of chromatin accessibility (chromBPNet)chipseq_pipeline
AQUAS TF and histone ChIP-seq pipelinedfim
Deep Feature Interaction Maps (DFIM)ChromDragoNN
Code for the paper "Integrating regulatory DNA sequence and gene expression to predict genome-wide chromatin accessibility across cellular contexts"3DChromatin_ReplicateQC
Software to compute reproducibility and quality scores for Hi-C dataalzheimers_parkinsons
Collaboration with Montine, Chang, and Montgomery labs on Alzheimers / Parkinson's ATAC-seq analysisgenomelake
Simple and efficient access to genomic data for deep learning models.simdna
A python library for creating simulated regulatory DNA sequencesabstention
Algorithms for abstention, calibration and domain adaptation to label shift.coda
Coda: a convolutional denoising algorithm for genome-wide ChIP-seq datacs273b
CS273B Deep Learning for Genomics Course MaterialsENCODE_downloader
Downloader for ENCODEcoessentiality
Companion to "A genome-wide almanac of co-essential modules assigns function to uncharacterized genes" (https://doi.org/10.1101/827071)genomedisco
Software for comparing contact maps from HiC, CaptureC and other 3D genome data.training_camp
Genetics training campgkmexplain
Accompanying repository for GkmExplain paperfastISM
In-silico Saturation Mutagenesis implementation with 10x or more speedup for certain architectures.ataqc
basepairmodels
labelshiftexperiments
Label shift experimentsseqdataloader
Sequence data label generation and ingestion into deep learning modelsbpnet-manuscript
BPNet manuscript code.higlass-dynseq
Dynamic sequence track for HiGlassDeepBindToKeras
Convert DeepBind models to KerasProCapNet
Repository for modeling PRO-cap data with the BPNet-like model, ProCapNet.MPRA-DragoNN
Code accompanying the paper "Deciphering regulatory DNA sequences and noncoding genetic variants using neural network models of massively parallel reporter assays"mpra
Deep learning MPRAsENCODE_scatac
variant-scorer
A framework to score and analyze variant effects genome-wide using ChromBPNet modelstronn
Transcriptional Regulation (Optimized) Neural Nets (TRoNN)Cardiogenesis_Repo
Cardiogenesis Repodeepbind
I have put my modified version of the deepbind code here.scATAC-reprog
Code for the analysis performed in the paper "Transcription factor stoichiometry, motif affinity and syntax regulate single-cell chromatin dynamics during fibroblast reprogramming to pluripotency" by Nair, Ameen et al.veryolddontuse_deeplift_modisco_tutorial
chromovar3d
Code from the chromatin variation 3d projectchip-nexus-pipeline
ChIP-nexus pipelinekerasAC
keras accessibility models: code to train, predict, interpretDART-Eval
DMSO
mesoderm
Scripts for dataset processing and QC for the mesoderm differentiation project.1kg_ld_utils
utils/notes for LD calculation from 1000 genomes panelkeras-genomics
Genomics layers for Keras 2lsgkm-svr
lsgkm+gkmexplain with regression functionality. Builds off kundajelab/lsgkm (which has gkmexplain), which in turn builds off Dongwon-Lee/lsgkm (the original lsgkm repo)yuzu
yuzu is a compressed-sensing based approach for quickly calculating in-silico mutagenesis saliency.PFBoost
modular 2D boosting code with stabilization and hierarchiescoessentiality-browser
Gene browser using coessentiality and related datazenodo_upload
Python script to upload files to Zenodoneural_motif_discovery
Framework for interrogating transcription-factor motifs and their syntax/grammars from neural-network interpretationsvizsequence
Collecting commonly-repeated sequence visualization code hereav_scripts
A place to track my scripts with git.bpnet-refactor
dynseq-pages
locusselect
extraction of data embeddings from deep learning model layers; computation of embedding distance and visualization with umap/tsneatlas_resources
A nucleotide-resolution, context-specific sequence annotation of the dynamic regulatory landscape of the human and mouse genomestf_binding_challenge
scoring/ranking code for tf binding challengebulk-rna-seq
Pipeline for gecco RNA-seq analysispython_reading_group
higlass-multi-tileset
Multi-tileset data fetcher for HiGlassretina-models
BPNet models for retina single-cell multiome dataTF-Atlas
Code repository for the TF-Atlas projectcrispr_safe_targeting_regions
Repository for creating the CRISPR controls termed "safe harbor" regions from Morgens et al., 2017, Nat Comms.interpret-benchmark
Benchmarking interpretation methodskCCA
momma_dragonn
Flexible deep learning frameworkfeature_interactions
bds_pipeline_modules
BigDataScript (BDS) pipelines and modulesmseqgen
Multi task batch generator for training deep learning models on CHIP-seq, CHIP-exo, CHIP-nexus, ATAC-seq, RNA-seq (or any other -seq)SVM_pipelines
jamboree-toolkit
toolkit for setting up compute environment on gcp for jamboreesgenomics-DL-archsandlosses
A collection of Deep Learning architectures and loss functions from across the genomics literatureaffinity_distillation
SeqPriorizationCATLAS
Sequence priorization using gkm-explain.chromBPNet-tutorial
How to train BPNets on ATAC-seq data using the Basepairmodels repo from Stanford's Kundaje Lab.PREUSS
PREUSS: predicting RNA editing using sequence and structureCTCFMutants
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