seharvey2012's Stars
TrinityCTAT/CTAT-LR-fusion
fusion transcript detection using long reads, leveraging ctat-minimap2 and FusionInspector
ratschlab/pancanatlas_code_public
Public repository containing research code for the TCGA PanCanAtlas Splicing project
jlevy44/AutoParisX
ksugar/qupath-extension-sam
QuPath extension for Segment Anything Model (SAM)
pmqs/Fix-OneDrive-Zip
Fix OneDrive Zip files >4Gig
IrinaVKuznetsova/CirGO
andreped/NoCodeSeg
🔬 Code-free deep segmentation for computational pathology
HenriquesLab/ZeroCostDL4Mic
ZeroCostDL4Mic: A Google Colab based no-cost toolbox to explore Deep-Learning in Microscopy
PingjunChen/pycontour
Contour python toolkit
williamritchie/IRFinder
Detecting intron retention from RNA-Seq experiments
ksahlin/pyinfor
some of my codes on bioinformatics with python
JohnUrban/LexoNSseq2015
Contains notes and custom scripts used to analyze Illumina reads for our NS-seq paper.
YeoLab/gffutils
GFF and GTF file manipulation and interconversion
ChangLab/FAST-iCLIP
Fully Automated and Standardized (FAST) iCLIP analysis pipeline.
YeoLab/clipper
A tool to identify CLIP-seq peaks
alexdobin/STAR
RNA-seq aligner
joshuagryphon/plastid
Position-wise analysis of sequencing and genomics data
zqfang/GSEApy
Gene Set Enrichment Analysis in Python
tanghaibao/goatools
Python library to handle Gene Ontology (GO) terms
mandel01/programming-for-biologists
Programming for Biologists workshop series at Northwestern University Chicago Campus