DupFinder: A tools to detect the duplicated genes using Illumina and Nanopore sequencing data
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Updated
Sep 13, 2023 - Nextflow
DupFinder: A tools to detect the duplicated genes using Illumina and Nanopore sequencing data
Automated Tool for Global Screening Array analysis
Code related to immunogenomics projects
Presentation delivered at the 2017 EUPHRESCO workshop in Edinburgh, 1st November 2017
Jackson Labs Summer Student Program 2018, Bar Harbor, ME. Statistically analyzing the effect of genetic diversity on the aging heart. Final paper: https://docs.google.com/document/d/1rkDRjnS6XhkFGk6EpzB4V24XqJdfN_JaM4vh5cc3iBA/edit
Hilbert Mapper is a C++ implementation of Hilbert's space filling curve to represent read coverage on genomic sequences. Although it can be used to represent any unidimensional vector of positive numerical data.
A collection of classes and methods for the analysis of 3C-based sequencing data.
Web application for HBV-GLUE
A nextflow pipeline to run phylogenetic analyses using SNPs
Computer Science Infotainment. Tribute to the Article Series in Scientific American and their german release Spektrum der Wissenschaft
Converts DNA input to amino acid sequence.
A small repo that eases use of google's deepvariant with GWA metastudies about hypertension
An R package to generate heatbox and scatter plots from a feature matrix.
pedigree file parsing and relatedness calculations for nim
Clincal Biospecimen Portal
Scientific workflow engine designed for simplicity & scalability. Trivially transition between one off use cases to massive scale production environments
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