There are no reviews yet. Be the first to send feedback to the community and the maintainers!
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)phantompeakqualtools
This package computes informative enrichment and quality measures for ChIP-seq/DNase-seq/FAIRE-seq/MNase-seq data. It can also be used to obtain robust estimates of the predominant fragment length or characteristic tag shift values in these assays.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 analysishiglass-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
Love Open Source and this site? Check out how you can help us