Pinned Repositories
CNprep
CNprep Package - Pre-process DNA Copy Number (CN) Data for Detection of CN Events
CNVMetrics
R Package to compare copy number variant (CNV) results from multiple samples/methods
conda-recipes
NormaFlyze
OrganoidsToolBox
Enabling organoid analyses using drug sreening, RNA-seq, exome-seq
p53-LOH-figures
RAIDS
Accurate and robust inference of genetic ancestry from cancer-derived molecular data across genomic platforms
SCclust
Segmentation and Clustering of Single Cell Sequencing Copy Number Profiles
SCGV
SCGV is an interactive graphical tool for single-cell genomics data, with emphasis on single-cell genomics of cancer
sgains
Sparse Genomic Analysis of Individual Nuclei by Sequencing
KrasnitzLab's Repositories
KrasnitzLab/SCGV
SCGV is an interactive graphical tool for single-cell genomics data, with emphasis on single-cell genomics of cancer
KrasnitzLab/RAIDS
Accurate and robust inference of genetic ancestry from cancer-derived molecular data across genomic platforms
KrasnitzLab/CNVMetrics
R Package to compare copy number variant (CNV) results from multiple samples/methods
KrasnitzLab/CNprep
CNprep Package - Pre-process DNA Copy Number (CN) Data for Detection of CN Events
KrasnitzLab/OrganoidsToolBox
Enabling organoid analyses using drug sreening, RNA-seq, exome-seq
KrasnitzLab/sgains
Sparse Genomic Analysis of Individual Nuclei by Sequencing
KrasnitzLab/conda-recipes
KrasnitzLab/NormaFlyze
KrasnitzLab/p53-LOH-figures
KrasnitzLab/SCclust
Segmentation and Clustering of Single Cell Sequencing Copy Number Profiles
KrasnitzLab/sgains_docker