Personal Website with Blogposts, Achievements and Ideas
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Updated
Jun 3, 2024 - HTML
Personal Website with Blogposts, Achievements and Ideas
An R package for detecting copy number variants from SNPs data
Supporting material to the study of "The behavior of mean fitness during range expansions in different dimensions". You can find the full link at .
VarFish: comprehensive DNA variant analysis for diagnostics and research
Genome annotation based on Rust and RocksDB
Open Targets python framework for post-GWAS analysis
GORpipe is a tool based on a genomic ordered relational architecture and allows analysis of large sets of genomic and phenotypic tabular data using declarative query language, in a parallel execution engine.
This repository is dedicated to advancing precision medicine through Python-based bioinformatics analyses. It emphasizes genomic data processing, analysis of genetic variability, and the development of predictive models that tailor healthcare to individual genetic profiles.
Clinvar data builds for annonars
Get standard bioinformatics stats, and more, for your DNA or RNA sequence.
Making Structural Equation Modeling (SEM) in R quick & powerful
The home of the FlyBase miscellaneous ontologies - incorporating the Drosophila Phenotype Ontology (see also FlyBase/drosophila-phenotype-ontology)
Pipeline for variant annotation using Variant Effect Predictor (VEP)
VEP-like tool for sequence ontology and HGVS annotation of VCF files
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