Pinned Repositories
grantn5
Config files for my GitHub profile.
infercnvpy
Infer copy number variation (CNV) from scRNA-seq data. Plays nicely with Scanpy.
maftools
Summarize, Analyze and Visualize MAF files from TCGA or in-house studies.
modules
Repository to host tool-specific module files for the Nextflow DSL2 community!
sarek
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
website
Code and files for the main nf-core website.
infercnvpy
Infer copy number variation (CNV) from scRNA-seq data. Plays nicely with Scanpy.
sarek
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
maftools
Summarize, Analyze and Visualize MAF files from TCGA or in-house studies.
varlociraptor
Flexible, uncertainty-aware variant calling with parameter free filtration via FDR control.
grantn5's Repositories
grantn5/grantn5
Config files for my GitHub profile.
grantn5/infercnvpy
Infer copy number variation (CNV) from scRNA-seq data. Plays nicely with Scanpy.
grantn5/maftools
Summarize, Analyze and Visualize MAF files from TCGA or in-house studies.
grantn5/modules
Repository to host tool-specific module files for the Nextflow DSL2 community!
grantn5/sarek
Analysis pipeline to detect germline or somatic variants (pre-processing, variant calling and annotation) from WGS / targeted sequencing
grantn5/website
Code and files for the main nf-core website.