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EDirectCookbook
TheHumanPangenome
A Strategy for Building and Using a Human Reference PangenomeCommunity_Software_Tools_for_NGS
NovoGraph
NovoGraph: building whole genome graphs from long-read-based de novo assembliesrnaseqview
RNA-seq Viewer Team at the NCBI-assisted Boston Genomics HackathonConsensusML
Machine Learning to Detect Cancer Biomarkers from RNAseq DataVirusDiscoveryProject
Software, architecture, and data index design for the 2018/2019 Virus Discovery Projectdrugdisco
A high throughput automated drug discovery pipeline.Pharmacogenomics_Prediction_Pipeline_P3
NCBIComputationalCookbook
Jupyter notebooks to more effectively leverage computational resources at NCBI.ViruSpy
A pipeline for viral identification from metagenomic samplesSPeW
Automatic Packaging and Distribution of Bioinformatics PipelinesMR_BACOn
Mendelian Randomization with Biomarker Associations for Causality with OutcomesMachine_Learning_Immunogenicity
This is a repo for the Machine Learning Immunogenicity Team in the August 2016 NCBI HackathonLabPype
Framework for Creating Pipeline SoftwareMetagenomicAntibioticResistance
NastyBugs: a simple method for extracting antimicrobial resistance information from metagenomesCTEligible
Use machine learning to find patterns of similar eligibility protocol criteria for clinical trialsRNA-Seq-in-the-Cloud
An Easy to Use Analysis System for All Human Public bulk RNAseq Data!Design-of-ICD-9-to-10-conversion-function-for-the-R-package-icd
Develop a function to be incorporated into the R package 'icd' that will convert International Classification of Diseases codes from Ninth to Tenth revisionsNetwork_SNPs
A framework for network analysis and display of SNPsSRA_Tinder
Find hot data sets in your area (of research)!ncbi-cloud-tutorials
Tutorial content for NCBI cloud data and computingMaster_gff3_parser
Convert sequence IDs between ucsc/refseq/genbankGoodDoc
A Template for Clear and Simple Documentation of Bioinformatics Codeseqacademy
Self-guided educational workshop for ChIP-Seq and RNA-SeqATACFlow
An ATAC-seq pipeline wrapped in NextFlow that can be run by Jupytersvcompare
Structural_Variant_Comparison
SVSemantic-search-log-analysis-pipeline
Classify web visitor queries so you can chart, and respond to, trends in information seekingPubRunner
Framework for running text mining tools on latest publications. Main page at:deVoReaNN
A virtual reality environment for physically assembling deep learning models to solve data science problems.seqr
HLAClustRView
R package specialized in HLA typing clustering and visualization based on specific similarity metricsphenotypeXpression
Subclassification of disease states based on the intersection of literature and expressionhackathon_v001_metagenomics
Metagenomics Pipeline Repository for January, 2015 NCBI/ADDS Hackathon at NIHFlowBio
A fast, easy way to present complex bioinformatics pipelines to biologistsGeneExpressionAging
Gene expression viewer templateThe-Broad-Institute-Single-Cell-RNA-Seq-Data-Set
Visualize cancer genomes with FAIR single-cell RNA-seq dataBiological-structure-segmentation-in-microscopy-images-using-deep-learning
TCGA_dbGaP
Virus_Detection_SRA
PrecisionMedicineToolkit
Search public databases for given genotypic informationBringing-the-Power-of-Synthetic-Data-Generation-to-the-Masses
We aim to make it easier for biomedical researchers to access and customize synthetic sequence data for the purpose of sharing and testing analysis methods as well as training and collaborationSimpleGeneExpression
Programs to quantify expression of transcripts from public datasetsMetabolomics-Data-Portal
R shiny application for the visualization and analysis of untargeted metabolomics datasets.deSRA
An automated protocol to extract variation or expression from public NGS datasetschervil
A detection algorithm for expression features that correspond to previous viral infectionStructural_Variants_CSHL
Kipoi-GWAS
VirusFriends
VirusFriends: discover viral sequences in the NCBI Sequence Read Archive!Got_Plasmid
Retreive and visualize plasmid sequences from SRA and Next Generation Sequencing data.Mutation_burden
Building a pipeline to assess effects of mutation burdenEpigenomics_CWL
SCREW: A Reproducible Workflow for Single-Cell EpigenomicsPhenVar
ClusterDuck
Disease Clustering from Literature Based on Minimal Training DataAssesSV
Code_in_PubMed_Abstracts
GeneHummus
An Automated Pipeline to Classify Gene Families based on Protein Domain Organization using Auxin Response Factors in Legumes as an ExampleClustering-autism-phenotypes-by-automated-text-analysis
A versatile tool to classify diseases using cluster analysis of published phenotypic dataHidden-Figures
A pipeline for inferring gender for acknowledged individuals in scientific literature on a massive scaleCancer_Epitopes_CSHL
A pipeline to approximate the immunogenicity of peptides resulting from cancer mutations based on structure and other factors.HASSL_Homogeneous_Analysis_of_SRA_rnaSequencing_Libraries
PubCode
An app platform for CLI Apps that engage NCBI/NLM Data and ServicesVirulence_Factor_Characterization
Virulence Factor Characterization in MetagenomesOnlineAdapterDatabase
Linking publicly deposited data to sequencing adapters.CapNetProtStruct
Capsule Networks for improving protein secondary structure prediction accuracyNCBI_Jupyter
A variety of NCBI Computational Tools Distributed as Jupyter NotebooksPSST
Polygenic SNP Search ToolEndoVir
Discovery of Novel Endogenous VirusesUPWARD
UPWARD: Uniting People Working Against Rare Diseasesclint
Linking clinical questions with fMRI research literatureTumor_sim
Simulation of Tumor Genomes -- Initiated at the 2017 NYGC-NCBI Hackathonhackathon_v001_rnaseq
RNAseq Pipeline Repository for January, 2015 NCBI/ADDS Hackathon at NIHRun_an_NCBI-style_hackathon
Collaborative Computational Development, or, How to Run an NCBI-Style HackathonSRA2R
SRA2R, a package to import SRA data directly into RTCRecePy
A python tool that uses Machine Learning to identify cancer targeting T-CellsAwesome_enhancer_promoter_dbs
A semi-curated list of enhancer and promoter databases. If you know of others, please put them in issues!CakeCell
Segmenting cells (and other objects!) in microscopy images via neural networks.ContainerInception
Gerber: Generalized Easy Reproducible Bioinformatics Environment wRapperMetadata_categorization
A crowdsourcing/expert curation platform for metadata categorization.DiseaseCluster
Disease prediction based on transcriptomics clusteringPuRSSE
Pubmed Research Search String Extraction (PuRSSE)Complex_Phenogeno
Mapping complex genotypes to phenotypic subclustersTriFECTA
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.RetroSpotter
A computational pipeline to find Human Endogenous Retroviruses in RNA Seq DataLNCPEP
A machine learning approach to detect micropeptides from noncoding RNAsVisualizing_MeSH_Term_Interaction_Over_Time
A tool to visually browse co-occurrence of MeSH terms in PubMebHistoloMaps
The fastest gigascale image annotation system in the world!ScrubSV
A QC pipeline for SVs calls based on coverage and SNP callsUltrafast_Mapping_CSHL
TraIN
Graph_Extraction
BarcSeek
BarcSeek: A Flexible Barcode Partitioning Tool for Demultiplexing Genomic Sequencing DataNCBI_August_Hackathon_Push_Button_Genomics_Solution
HAQmap
Push button solution for setting up an NCBI-style HackathonMutPredMerge
Consolidation of tools in the MutPred Suite to work with VCF filesPyClonal
Jupyter Notebooks to analyze T-cell Receptor SequencingViral-VDAP
Viral VDAP: a viral alignment, variant discovery, and annotation pipeline launched at the NCBI-Hackathon 2019ContamFilter
Implements NCBI Contamination Screen Publicly in CWLPubMed2GenePairs
Text-driven identification and ranking of associated gene pairs in PubMedLove Open Source and this site? Check out how you can help us