CriticalSci's Stars
gambalab/DREEP
Drug Response Estimation from single-cell Expression Profiles
stjude/ChIPseqSpikeInFree
A Spike-in Free ChIP-Seq Normalization Approach for Detecting Global Changes in Histone Modifications
yancychy/DiffChIPL
10XGenomics/supernova
10x Genomics Linked-Read Diploid De Novo Assembler
vierstralab/footprint-tools
A toolset to analyze genomic footprinting data
alelagana/MM-PSN
Multiple Myeloma Patient Similarity Network
jsh58/Genrich
Detecting sites of genomic enrichment
dahn-zk/zsh-jupyter-kernel
Z shell kernel for Jupyter Notebook
jdidion/biotools
A list of useful bioinformatics resources
loosolab/TOBIAS
Transcription factor Occupancy prediction By Investigation of ATAC-seq Signal
hyulab/PINTS
CshlSiepelLab/DENR
Select the most actively transcribed transcript model using PRO-seq
tuxera/ntfs-3g
NTFS-3G Safe Read/Write NTFS Driver
LHentges/LanceOtron
soimort/translate-shell
:speech_balloon: Command-line translator using Google Translate, Bing Translator, Yandex.Translate, etc.
zwang-bioinformatics/GOGO
An Improved Algorithm to Measure the Semantic Similarity of Gene Ontology Terms
Ayllonbe/gsan
stefanofranzini/essHIC
essHIC is a python module to compare HiC matrices by computing a metric distance between them
ktan8/ModTect
ModTect is a tool for identifying sites of RNA modifications that disrupts base-pairing using typical RNA-sequencing datasets
ChristopherWilks/megadepth
BigWig and BAM utilities
jupyterlab/jupyterlab-git
A Git extension for JupyterLab
meuleman/epilogos
Methods for summarizing and visualizing multi-biosample functional genomic annotations
genepattern/genepattern-notebook
Platform for integrating genomic analysis with Jupyter Notebooks.
deeptools/pyGenomeTracks
python module to plot beautiful and highly customizable genome browser tracks
GangCaoLab/CoolBox
Jupyter notebook based genomic data visualization toolkit.
tylermorganwall/rayshader
R Package for 2D and 3D mapping and data visualization
HillLab/SomaticSiMu
SomaticSiMu generates single and double base pair substitutions, and single base pair insertions and deletions of biologically representative mutation signature probabilities and combinations.
ay-lab/mustache
Multi-scale Detection of Chromatin Loops from Hi-C and Micro-C Maps using Scale-Space Representation
koszullab/chromosight
Computer vision based program for pattern recognition in chromosome (Hi-C) contact maps
clinicalml/ml_mmrf
Machine Learning with data from the Multiple Myeloma Research Foundation