An Easy to Use Analysis System for All Human Public bulk RNAseq Data!
Disease Clustering from Literature Based on Minimal Training Data
A complete rewrite of the original PhenVar to enhance functionality and maintainability
A web framework for interacting with drug safety data
A simple command line tool to map SRA reads with high accuracy
Automated combinatorial epitope analysis from TCR clones
Visualize cancer genomes with FAIR single-cell RNA-seq data
FAIRness assessment for NCBI Hackathon products
An automated protocol to extract variation or expression from public NGS datasets
Novel Discovery of Phages from Salmonella Sequences
The goal of this project is use natural language processing to extract exclusion and inclusion criteria from free form text fields to match patients with clinical trials.
NovoGraph: building whole genome graphs from long-read-based de novo assemblies
Virulence Factor Characterization in Metagenomes
Self-guided educational workshop for ChIP-Seq and RNA-Seq
An Automated Pipeline to Classify Gene Families based on Protein Domain Organization using Auxin Response Factors in Legumes as an Example
A Strategy for Building and Using a Human Reference Pangenome
A Pilot Project for Read Counts, Novel Transcripts and Population Level Functions in Metatranscriptomes
A Simple pipeline to use to predict metagenome medication interaction
Indexing and Visualization for AMRs and Virulence Genes in Genomes and Metagenomes
Software, architecture, and data index design for the 2018/2019 Virus Discovery Project
Develop a function to be incorporated into the R package 'icd' that will convert International Classification of Diseases codes from Ninth to Tenth revisions
A Robotic Encapsulation of a variant calling robot that can return deidentified results
Tutorial content for NCBI cloud data and computing
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