Repository for miscellaneous bioinformatics scripts that may be useful to others.
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Updated
Feb 7, 2017 - Python
Repository for miscellaneous bioinformatics scripts that may be useful to others.
Lift same species genome co-ordinates from one assembly to another
work for creating hg38 database files from hg19 sources
Inter-sample analysis of SQANTI classifications
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 Snakemake Workflow for using PolyA_DB and UCSC LiftOver with CellRanger
An efficient genetic data imputation pipeline
This toolkit deals with GEnomic sequence and genome structure ANnotation files between inbreeding lines and species.
Same species annotation lift over pipeline.
Lifterover copy number segments in whole
🚀 LiftOn: Accurate annotation mapping for GFF/GTF across assemblies
Convert genomic coordinates from the Human Genome version 19 (hg19) to version 38 (hg38)
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