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

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

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

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

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Enabling organoid analyses using drug sreening, RNA-seq, exome-seq

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Sparse Genomic Analysis of Individual Nuclei by Sequencing

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Segmentation and Clustering of Single Cell Sequencing Copy Number Profiles

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