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Showing results 8000

Complex trait regulatory architectures

Python 1 Updated Nov 11, 2017

UC Santa Cruz Computational Genomics Lab's Toil-based RNA-seq pipeline

Python 41 10 Updated Aug 17, 2020
Python 5 2 Updated May 1, 2018

Community-curated list of software packages and data resources for single-cell, including RNA-seq, ATAC-seq, etc.

3,427 1,022 Updated Jun 24, 2025

A collection of video resources for machine learning

1,547 214 Updated Jan 23, 2021

code for Structured Variational Autoencoders

Python 350 88 Updated Aug 22, 2018

Preprocessing of single-cell RNA-Seq (deprecated)

Jupyter Notebook 62 26 Updated Jul 5, 2019

Gaussian processes in TensorFlow

Python 1,878 430 Updated May 29, 2025

A small library for automatically adjustment of text position in matplotlib plots to minimize overlaps.

Jupyter Notebook 1,587 92 Updated Apr 22, 2025

📍 Repel overlapping text labels away from each other in your ggplot2 figures.

R 1,236 96 Updated Jun 16, 2025

Patsy Adaptors for Scikit-learn

Python 48 11 Updated Apr 17, 2019

pythonic wrapper for libhts (moved to: https://github.com/quinlan-lab/hts-python)

Python 49 18 Updated Mar 3, 2017

cyclone

HTML 18 12 Updated Jul 21, 2015

Near-optimal RNA-Seq quantification

C 692 175 Updated Apr 9, 2025

This repository is retired software

R 12 3 Updated Oct 29, 2015

Curve reconstruction from noisy points

R A0AB 1 Updated Mar 18, 2015

Gaussian processes framework in python

Python 2,102 566 Updated Jun 19, 2025

R package to model time series accounting for noise in the temporal dimension. Specifically designed for single cell transcriptome experiments.

TeX 15 4 Updated Sep 24, 2021

Maximum likelihood demultiplexing

C++ 47 14 Updated Feb 14, 2025

🐟 🍣 🍱 Highly-accurate & wicked fast transcript-level quantification from RNA-seq reads using selective alignment

C++ 811 168 Updated May 29, 2024

python / numpy / pandas / patsy version of ComBat for removing batch effects.

Python 105 44 Updated Dec 31, 2018

Fast, flexible and easy to use probabilistic modelling in Python.

Python 3,460 594 Updated Mar 6, 2025

scLVM is a modelling framework for single-cell RNA-seq data that can be used to dissect the observed heterogeneity into different sources, thereby allowing for the correction of confounding sources…

HTML 106 45 Updated Dec 16, 2022

Reproducible machine learning analysis of gene expression and alternative splicing data

Jupyter Notebook 126 25 Updated Apr 15, 2023

IsFinder find virus insertion site in host genomic DNA from pair end NGS data

Python 1 1 Updated Jul 31, 2014

The K-mer Analysis Toolkit (KAT) contains a number of tools that analyse and compare K-mer spectra.

C++ 216 50 Updated Nov 25, 2022

Rapid Mapping-based Isoform Quantification from RNA-Seq Reads

C++ 126 45 Updated Jun 9, 2022

GeneExpressMap makes possible the rapid, three-dimensional analysis of multiplex fluorescent whole mount in situ hybridizartion (F-WMISH) data at single cell resolution. It relies on the assignment…

Objective-C 1 Updated Jun 21, 2011

Mixture Models for Single Cell Assays

R 7 2 Updated Jun 1, 2021
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