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FluentDNA allows you to browse sequence data of any size using a zooming visualization similar to Google Maps. You can use FluentDNA as a standalone program or as a python module for your own bioinformatics projects.
A fast and efficient tool for converting chromatin interaction data between genome assemblies
🚀 LiftOn: Accurate annotation mapping for GFF/GTF across assemblies
This toolkit deals with GEnomic sequence and genome structure ANnotation files between inbreeding lines and species.
Lifterover copy number segments in whole
An efficient genetic data imputation pipeline
A crate for working with genomics chain files.
a python pipeline to generate chain files between different genome assemblies for LiftOver.
Repository for miscellaneous bioinformatics scripts that may be useful to others.
A Snakemake Workflow for using PolyA_DB and UCSC LiftOver with CellRanger
A Go-written server for 23andMe-formatted raw data liftover
Convert genomic coordinates from the Human Genome version 19 (hg19) to version 38 (hg38)
Inter-sample analysis of SQANTI classifications