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
PANDORA 💻
A modular annotation tool for genomic variants
The Visualization Multitool for Molecular Epidemiology and Bioinformatics
H.E.L.E.N. (Homopolymer Encoded Long-read Error-corrector for Nanopore)
RADseq Data Exploration, Manipulation and Visualization using R
Fast and precise comparison of genomes and metagenomes (in the order of terabytes) on a typical personal laptop
memory efficient, fast & precise taxnomomic classification system for metagenomic read mapping
Phigaro is a scalable command-line tool for predicting phages and prophages
stackr: an R package to run stacks software pipeline
R package: Simulate Expression data from igraph network using mvtnorm (CRAN; JOSS)
Shiny app for making and annotating Volcano plots
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:
genomic alignment similarity search tool
Collection of statistical scripts, image analysis workflows, data used in publications by the Misteli Lab.
Cartography of Genomic Interactions Enables Deep Analysis of Single-Cell Expression Data (Nature Communications, 2023)
Differential Privacy Protection against MembershipInference Attack on Machine Learning for Genomic Data
The AnnSQL package enables SQL based queries on AnnData objects.
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