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Justin Bedő

I am a researcher at the Walter and Eliza Hall institute in the Papenfuss lab. I work on machine learning and am interested in developing techniques for knowledge discovery in biological data. In particular, I'm interested in precision medicine.

=> Gemlog

Projects

=> Git repositories | GitHub

Machine learning methods for somatic genome rearrangement detection

Structural variants (SVs) are large-scale genomic changes and are an important type of mutation in cancer. SVs can occur through a variety of biological mechanisms leading to insertions, deletions, duplications, inversions, and translocations in the genome. These mutations can cause cancers and affect response to therapy. A student project is available to develop machine learning methods that generate the best possible results from whole genome tumour-normal sequencing data for each patient.

=> Papenfuss lab student projects

BioNix

BioNix is a tool for reproducible bioinformatics that unifies workflow engines, package managers, and containers. It is implemented as a lightweight library on top of the Nix deployment system. BioNix is currently in use at WEHI and is actively developed.

=> Git repository

svaRetro & svaNUMT

svaRetro and svaNUMT are R packages for detecting retrotransposed transcripts and mitocondrial insertions into the nuclear genome (NUMT) from structural variant calls.

=> svaRetro | svaNUMT

Recent publications

=> Google Scholar

Contact

=> GPG key | Matrix (@jb:vk3.wtf) | ORCID iD: 0000-0001-5704-0212

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