a framework for training sequence-level deep learning networks
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Updated
Dec 16, 2024 - Jupyter Notebook
a framework for training sequence-level deep learning networks
A modular annotation tool for genomic variants
PANDORA 💻
The Visualization Multitool for Molecular Epidemiology and Bioinformatics
Fast and precise comparison of genomes and metagenomes (in the order of terabytes) on a typical personal laptop
H.E.L.E.N. (Homopolymer Encoded Long-read Error-corrector for Nanopore)
memory efficient, fast & precise taxnomomic classification system for metagenomic read mapping
RADseq Data Exploration, Manipulation and Visualization using R
Phigaro is a scalable command-line tool for predicting phages and prophages
The AnnSQL package enables SQL based queries on AnnData objects.
Shiny app for making and annotating Volcano plots
R package: Simulate Expression data from igraph network using mvtnorm (CRAN; JOSS)
(current) A NGS analysis framework for WGS data, which automates the entire process of spinning up AWS EC2 spot instances and processing FASTQ to snvVCF in <60m, for dollars a sample and achieving Fscores of 0.998.
Genome Contact Map Explorer - gcMapExplorer. Visit:
Differential Privacy Protection against MembershipInference Attack on Machine Learning for Genomic Data
Cartography of Genomic Interactions Enables Deep Analysis of Single-Cell Expression Data (Nature Communications, 2023)
genomic alignment similarity search tool
Collection of statistical scripts, image analysis workflows, data used in publications by the Misteli Lab.
[G]enomic [P]ositioning with [Py]thon
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