Hi, thank you for developing such a great tool. I have single-cell long-read and short-read RNA-seq data from same cells using 10X 5' kit and want to utilize SNV called from long-read and CNV called from short-read to conduct phylogeny analysis of tumor cells. Do you think this would work on COMPASS?
Hi, thank you for developing such a great tool. I have single-cell long-read and short-read RNA-seq data from same cells using 10X 5' kit and want to utilize SNV called from long-read and CNV called from short-read to conduct phylogeny analysis of tumor cells. Do you think this would work on COMPASS?