Unix, R and python tools for genomics and data science
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Updated
Dec 19, 2024 - Shell
Unix, R and python tools for genomics and data science
Bioinformatics on GCP, AWS or Azure
A neoantigen calling pipeline begins from variants record file (MAF) (Not maintain now)
Set of commandline tools for analysis of tumor variants without a matching normal. Method described in Genome Research: http://genome.cshlp.org/content/25/9/1382.full
Docker container to download dbNSFP 'database' and wrangle it into a format suitable for pipeline annotation process
Pipeline to filter whole exome vcf files and generate a report document for clinical diagnostics.
Downloading and processing pipelines used for single cell gene expression assays of human tumor biopsies
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