NCBI Hackathons!


Events

June 19-21 New York Genome Center
August 17-19, NIH Campus
September 25-27, Pittsburgh, PA
January 8-10, NIH Campus
February 19-21, Baylor College of Medicine
March 11-14, NIH Campus
May 15-17, 2018, Ann Arbor, MI

Github Hackathon Webpage Updates

DangerTrack
A system for evaluating difficult to assess regions that uses SV calls and mappability to generate a genome-wide score
Master_gff3_parser
SeqIDMapper provides naming consistency in these input files by converting the sequence feature IDs in the entire file to the desired ID format using a single command
ga4gh-ncbi-api
Making NCBI data available using GA4GH methods
Graph_Extraction
Motivate the transition to graph genomes, we developed a simple graph-based genome browser that is accessible at http://graphymcbrowserface.umbc.in
Virus_Detection_SRA
Sidearm searches the SRA database for viruses using the NCBI magicBLAST tool
Scan2CNV
Generate CNV calls from raw SNP array data using the command line.
Epigenomics_CWL
A CWL Pipeline and Docker Image for Performing Standard Single-Cell DNA Methylation Analyses
PhenVar
PubMed2GenePairs
Text-driven identification and ranking of associated gene pairs in PubMed
Visualizing_MeSH_Term_Interaction_Over_Time
A tool to visually browse co-occurrence of MeSH terms in PubMeb
PubRunner
Framework for running text mining tools on latest publications.
svcompare
Comparison and estimation of breakpoints for SVs across different technologies and resources.
Structural_Variant_Comparison
Tools to compare structural variants to those in public databases!
Structural_Variants_CSHL
10x genomics read simulator, topsorter and danger track.
SRA2R
An R package for using the SRA toolki
Ultrafast_Mapping_CSHL
Finding expressed variants while streaming data.
RNA_mapping
A self-guided hands-on RNAseq tutorial designed to run for free on cloud services.
rnaseqview
An ideogram-based viewer for whole transcriptome RNAseq experiments.
Code_in_PubMed_Abstracts
This tool searches for code cited in PubMed abstracts by searching for popular repositories such as GitHub and Bitbucket.
Network_SNPs
MetaNetVar is a pipeline for applying network analysis tools for genomic variant analysis.
Network_Stats_Acc_Interop
SNP FSA is a pipeline for applying statistical analysis tools to identify interactions between SNPs and their effects on phenotypic expression.
3D_2D_Rep_Structure
Tool to create 2D diagrams from 3D protein structures and render them side by side.
iCN3D-MMTF
Ultrafast transfer of protein structure information from pdb to the NCBI iCN3D viewer
PDB2Genome
Mapping PDB structures to gene-level in genome browsers, and visualizing SNPs
Metadata_categorization
A crowdsourcing/expert curation platform for metadata categorization
TCGA_dbGaP
The repository contains scripts to automatically fetch related dbGaP studies and subsequently the specific sequence files for given TCGA data.
Machine_Learning_Immunogenicity
A pipeline to learn about the immunogenicity of peptides based on prior data using TensorFlow.
Cancer_Epitopes_CSHL
A pipeline to approximate the immunogenicity of peptides resulting from cancer mutations based on structure and other factors.

Representative manuscripts
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