GenomicDataCommonsProvide R access to the NCI Genomic Data Commons portal.
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bystroBystro genetic analysis (annotation, filtering, statistics)
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mcscanCommand-line program to wrap dagchainer and combine pairwise results into multi-alignments in column format
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reg-genRegulatory Genomics Toolbox: Python library and set of tools for the integrative analysis of high throughput regulatory genomics data.
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catchA package for designing compact and comprehensive capture probe sets.
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tiptoftPredict plasmids from uncorrected long read data
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dagger2-ktxKotlin extension bridge library for Dagger2 (proof-of-concept)
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annotated research papersThis repo contains annotated research papers that I found really good and useful
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companionThis repository has been archived, currently maintained version is at https://github.com/iii-companion/companion
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WinAnalyticsA light-weight android library that can be quickly integrated into any app to use analytics tools.
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netSmoothnetSmooth: A Network smoothing based method for Single Cell RNA-seq imputation
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saffrontreeSaffronTree: Reference free rapid phylogenetic tree construction from raw read data
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jupyter-bbox-widgetA Jupyter widget for annotating images with bounding boxes
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SingleFile-LiteFeel the power of the Manifest V3. The future, right now!
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fermikitDe novo assembly based variant calling pipeline for Illumina short reads
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grenade[DEPRECATED] Annotation based intent builder for Android activities and services
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mapcompGenetic Map Comparison
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gff3toemblConverts Prokka GFF3 files to EMBL files for uploading annotated assemblies to EBI
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dropClustVersion 2.1.0 released
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switchdeInference of switch-like differential expression along single-cell trajectories
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IntDefsAndroid constants wrapped in @IntDef annotations
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dna-traitsA fast 23andMe genome text file parser, now superseded by arv
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pandas-stubsPandas type stubs. Helps you type-check your code.
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ntHashFast hash function for DNA sequences
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23andme2vcfconvert your 23andme raw file to VCF | DEPRECATED, please see https://github.com/plantimals/2vcf
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chromapFast alignment and preprocessing of chromatin profiles
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GenomeAnalysisModuleWelcome to the website and github repository for the Genome Analysis Module. This website will guide the learning experience for trainees in the UBC MSc Genetic Counselling Training Program, as they embark on a journey to learn about analyzing genomes.
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py2pumlGenerate PlantUML class diagrams to document your Python application.
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coolpuppyA versatile tool to perform pile-up analysis on Hi-C data in .cool format.
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plasmidtronAssembling the cause of phenotypes and genotypes from NGS data
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viralrecallDetection of NCLDV signatures in 'omic data
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alfresco-mvcGlue between SpringMVC @controllers and Alfresco
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videojs-annotation-commentsA plugin for video.js to add support for timeline moment/range comments and annotations
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bacnetBACNET is a Java based platform to develop website for multi-omics analysis
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CAMSACAMSA: a tool for Comparative Analysis and Merging of Scaffold Assemblies
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FALDOFeature Annotation Location Description Ontology
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PHANOTATEPHANOTATE: a tool to annotate phage genomes.
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smartas📓Notebook of Climente-González et al. (2017), The Functional Impact of Alternative Splicing in Cancer.
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memoAndroid processing and secured library for managing SharedPreferences as key-value elements efficiently and structurally.
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staramrScans genome contigs against the ResFinder, PlasmidFinder, and PointFinder databases.
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EarlGreyEarl Grey: A fully automated TE curation and annotation pipeline
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calN50Compute N50/NG50 and auN/auNG
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MAGMA CelltypingFind causal cell-types underlying complex trait genetics
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rare-disease-wf(WIP) best-practices workflow for rare disease
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coreThe XP Framework is an all-purpose, object oriented PHP framework.
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AutoBindingsSet of annotations that aims to make your Android development experience easier along with lint checks.
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OntologiesHome of the Genomic Feature and Variation Ontology (GFVO)
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arcsvComplex structural variant detection from WGS data
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the schema isActiveRecord schema annotations done right
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cloud-genomicsIntroduction to Cloud Computing for Genomics
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SubstanceA JavaScript library for web-based content editing.
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mccortexDe novo genome assembly and multisample variant calling
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awesome-geneticsA curated list of awesome bioinformatics software.
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