A tutorial on structural variant calling for short read sequencing data
-
Updated
Oct 24, 2024 - R
A tutorial on structural variant calling for short read sequencing data
Comprehensive design of CRISPR gRNAs for nucleases and base editors
This repository serves as a valuable resource for individuals engaged in data exploration, statistical analysis, and research within the domains of plant breeding, genetics, statistics, and genomics. The purpose of this repository is to share a collection of R codes that can be utilized by others for their own data analysis projects
Structural variant calling tutorial using long-reads.
R package for annotating and parsing transposable elements-associated data
Genetic Algorithm implementation to study haplotypes of genomic features
This repository is the current repository for our Jones et al. 2024 manuscript titled Long-read RNA sequencing identifies region- and sex-specific C57BL/6J mouse brain mRNA isoform expression and usage.
Framework for investigation of cell-type-specific regulation and expression in rare disease
Scripts used for analysis of single cell RNA-Seq data presented in Markos 2024 paper.
Data for Smith et al. 2021 in Ecology and Evolution
This is a TxDb package created for Coffea arabica (coffee).
Sparse factorization framework to integrate GWAS studies and identify shared latent genetic components
To perform RNA-Seq data analysis and calculate length-scaled transcripts per million (TPM) values using the Salmon tool and the GenomicFeatures package in R.
Add a description, image, and links to the genomics-analysis topic page so that developers can more easily learn about it.
To associate your repository with the genomics-analysis topic, visit your repo's landing page and select "manage topics."