A genome visualization python package for comparative genomics
-
Updated
Jun 14, 2026 - Python
A genome visualization python package for comparative genomics
Python programs for processing GFF3 files
convert various features into a GFF-like file for use in genome browsers
Efficiently keep track of changes to genomes
scripts for RNA-Seq analysis
command lines tool to annotate miRNAs with a standard mirna/isomir naming
Convert sequence IDs between ucsc/refseq/genbank
CRISPR/Cas-directed HDR genome editing suite: finds+scores gRNA targets, generates donor DNAs, & produces optimal cPCR primer designs.
🧬 GFFBase — Rust+DuckDB GFF3/GTF engine
Gff-toolbox is a toolbox of commands that enables one to get the gist of their GFF annotation files, as well as to analyse them in different ways.
Bio-Wrangler is a Python package for bioinformatics data wrangling. It helps load, filter, merge, and summarize bioinformatics datasets from formats like FASTA, FASTQ, VCF, and GFF.
This pipeline infers exon functional annotations using coordinates from a .gff file and derives corresponding intron coordinates along with relevant annotations. Users can optionally specify the length of intronic fragments to extract. The pipeline is suited for splicing code analyses.
Predicting Transcription Factor Binding Sites from ENCODE data using Machine Learning
To associate your repository with the gff topic, visit your repo's landing page and select "manage topics."