KrasnitzLab

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1. SCGV SCGV Public

   SCGV is an interactive graphical tool for single-cell genomics data, with emphasis on single-cell genomics of cancer

   Python 8 2

2. RAIDS RAIDS Public

   Accurate and robust inference of genetic ancestry from cancer-derived molecular data across genomic platforms

   R 7 4

3. CNVMetrics CNVMetrics Public

   R Package to compare copy number variant (CNV) results from multiple samples/methods

   R 4 2

4. CNprep CNprep Public

   CNprep Package - Pre-process DNA Copy Number (CN) Data for Detection of CN Events

   R 3 2

5. sgains sgains Public

   Sparse Genomic Analysis of Individual Nuclei by Sequencing

   Python 1 1

6. SCclust SCclust Public

   Segmentation and Clustering of Single Cell Sequencing Copy Number Profiles

   R 1 1