Reference-based consensus creation
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Updated
Sep 15, 2026 - Nextflow
Reference-based consensus creation
The BiomolecularStructures package provides several Bioinformatics-related modules for Julia.
Auditable agent skill for resolving protein queries, selecting references, and planning reproducible phylogenetic trees.
Some scripts to make your bioinformatics analyses reproducible and a bit easy 🤓
Automated maximum-likelihood phylogeny pipeline for viral families. Discovers species via NCBI Taxonomy, downloads from GenBank, aligns with MAFFT, builds trees with FastTree (broad) and IQ-TREE (refined), and annotates internal nodes by LCA. Supports multi-marker concatenation for large DNA virus families.
DesignLab — conservation-aware PCR/qPCR primer design: NCBI search, MAFFT alignment, conserved-block Primer3 design and in-silico validation, with every binding site visualised
Modular Python bioinformatics library for genomic sequence analysis. Read preparation, assembly, homology search, clustering, multiple sequence alignment, and mapping as installable CLIs and importable modules.
DNA pairwise alignment, difference analysis, coordinate mapping and visualization tool.
Representative sequence selection for large bioinformatics datasets
A Python script that align SARS-CoV-2 genomes identifying and reporting pointwise variations.
This pipeline automates the process of generating phylogenetic trees from sequence data, specifically designed for high-throughput and efficient analysis.
🦇🦠🌳Study on detection of Brno loanvirus in Southern Russia
A bioinformatics pipeline for the systematic identification and evolutionary analysis of MADS-box gene families. Utilizes advanced genomic screening to trace plant developmental genetics and evolutionary lineages.
GUI and CLI workflow for phylogenetic tree construction, tanglegram comparison, and optional Foldseek protein-structure similarity.
Codon-aware phylogenetic pipeline with Snakemake
Graph-based pangenomic and synteny analysis of Helicobacter pylori (n=41 complete RefSeq genomes) using PPanGGOLiN, with reproducible workflows for annotation (Prokka), ANI quality control (FastANI), core-genome phylogeny (MAFFT + IQ-TREE 2), resistome profiling (AMRFinderPlus), and publication-grade visualizations.
Influenza antiviral resistance interpretation pipeline using amino acid sequences and WHO mutation rules.
Developed a bioinformatics workflow for the classification and functional characterization of the CAZy GH5 glycoside hydrolase family, a highly diverse enzyme family involved in carbohydrate metabolism.
This project performs an automated phylogenetic analysis of nucleotide sequences retrieved from NCBI. The pipeline includes sequence alignment, concatenation, phylogenetic inference (maximum likelihood, maximum parsimony, and Bayesian), and formatting for visualization.
Python toolkit for interpretable influenza HA mutation-tree analysis
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