De novo construction of isoforms from long-read data
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Updated
Sep 9, 2026 - Rust
De novo construction of isoforms from long-read data
Bioinformatics 101 tool for counting unique k-length substrings in DNA
Make phylogenetic trees and lineages from the NCBI Taxonomy database
A Rust library and CLI tool to handle genomic transcripts
Eidolon is a Rust implementation of the next-gen sequencing toolkit (NEAT). Eidolon features expanded features, including the ability to model cancer genetics, complex variants, location aware variant placement, and allele dosage.
A fast and memory-efficient FASTX PCR deduplication tool.
A small fasta CLI toolkit developed in Rust
A WASM genbank viewer to look through your sequences!
Bioinformatics Dependencies Platform - A better way to manage your bioinformatics data sources, search and query across multiple bioinformatics databases, tooling. Properly version and reproduce your research, generate citation and data acessibility statement.
Fast and accurate sample swap identification
A synthetic FASTQ record generator with pattern spiking
Lossless, biologically aware compression for sequence-containing files in FASTA format (e.g. .fasta, .fna)
Bioinformatics CLI tool for analysis and visualization
Rust-based implementation of grpaf.py from Truvari. Can do AF calculation, can not do HWE calculation.
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