Roy Granit, PhD's Projects
Infer copy number variation (CNV) from scRNA-seq data. Plays nicely with Scanpy.
Create beautiful, publication-quality books and documents from computational content.
Run the bedtools merge command on multiple files
An R script to do some QC on MinION data
Script that converts MSigDB '.gmt' files into a tab-delimited gene-set ready for use in 'Genomica'
Aggregate results from bioinformatics analyses across many samples into a single report.
Pathoscope: Species identification and strain attribution with unassembled sequencing data
Calculate the Pearson correlation between all genes in a given matrix
Config files for my GitHub profile.
An R shiny based tool used for single cell RNA-seq data visualization and analysis.
A parser for Google Scholar, written in Python
💫 Industrial-strength Natural Language Processing (NLP) in Python
A simple tags input with typeahead (autocomplete) built with Vue.js 2.