A collection of Python modules equivalent to R ReQTL Toolkit aims to identify the association between expressed SNVs with their gene expression using RNA-sequencing data.
-
Updated
Jan 20, 2022 - Python
A collection of Python modules equivalent to R ReQTL Toolkit aims to identify the association between expressed SNVs with their gene expression using RNA-sequencing data.
Use R snippets as python functions. Manage R dependencies separately.
Code and writings for my internship project at the Transcriptomic Bioinformatics research group at University Medical Center Groningen.
Graphical user interface allows easy access to the multiscale model-free idealization methods in the R-package clampSeg (https://cran.r-project.org/package=clampSeg). It supports the model-free segmentation methods JSMURF (https://ieeexplore.ieee.org/document/6655999), JULES (https://ieeexplore.ieee.org/document/8374882) and HILDE (https://arxiv…
Algorithm in python to determine how many people had stroke by age using linear regression
A complete python interface to Racmacs via rpy2
Instant Data Report using R packages 'DataExplorer' in Python
Advanced scanpy environment with R support (rpy2)
Python and R scripts written to perform some cleaning work on a dataset of Smithsonian Trinomials taken from American Antiquity issues ranging from 2004 to 2013.
NBA Player of the Week Visualizations using ggplot
COVID 19 state wise + India + International prediction with data visualization and live curve prediction
PROFILE RNA-seq binarization technique.
Add a description, image, and links to the rpy2 topic page so that developers can more easily learn about it.
To associate your repository with the rpy2 topic, visit your repo's landing page and select "manage topics."