Simulate Variants for provided genomic coordinates
-
Updated
Feb 21, 2022 - Python
Simulate Variants for provided genomic coordinates
An R package designed for generalized linear mixed model inference in genomic sequencing studies
Basic string utilities for Solidity
Enrichment analysis of motifs with ancient and recent CNEs
Biblioteca para análise de genômica de resistência a antibióiticos.
We are taking existing orthoMcl Software Written Perl and Translating it to Python
R package with sourced, original, and wrappers to functions I like and find recurrently useful.
Package to genomic prediction focused on GE genomic models
Short Sequence Rastreator allows genetic diversity analysis and preparation of input files for other softwares such as STRUCTURE, DARwin and SPAGeDi.
The R code was developed to draw the genomic track of signals for next-generation sequencing data.
This repository contains the answers for coursera 's "Bioconductor for Genomic Data Science"
A tool for calculating the Burrows-Wheeler transform (BWT) in a Map-Reduce fashion on Apache Spark Framework.
Comparison of sequencing read mapping to pangenome graphs
Add a description, image, and links to the genomic topic page so that developers can more easily learn about it.
To associate your repository with the genomic topic, visit your repo's landing page and select "manage topics."