Genome biologyBioinformaticsPeer-reviewed journal article
SlideCNA: Spatial copy number alteration detection from Slide-seq-like spatial transcriptomics data
Diane ZhangiD, Åsa SegerstolpeiD, Michal SlyperiD, Julia WaldmaniD, Evan M. MurrayiD, Ralf Strasser, Jan WatteriD, Ofir CoheniD, Orr AshenbergiD, Daniel L. AbravaneliD, Judit Jané‐ValbuenaiD, Simon MagesiD, Ana LakoiD, Karla E. HelvieiD, Orit Rozenblatt–RoseniD, Scott J. RodigiD, Fei CheniD, Nikhil WagleiD, Aviv RegeviD, Johanna KlughammeriD
Abstract
Solid tumors are spatially heterogeneous in their genetic, molecular and cellular composition, and this variation can be meaningful for diagnosis, prognosis and therapy. Recent spatial profiling studies have mostly charted genetic and RNA variation in tumors separately. To leverage the potential of RNA to identify copy number alterations (CNAs), we developed SlideCNA, a computational tool to extract sparse spatial CNA signals from spatial transcriptomics data, using expression-aware spatial binning. We test SlideCNA on simulated and real Slide-seq data of metastatic breast cancer (MBC) and demonstrate its potential for spatial sub-clone detection.
- organism: human
- assay: spatial transcriptomics
- research focus: clustering
- research focus: differential expression
- research focus: cell type annotation
- approach: statistical model
- Citations
- 4
- FWCI
- 1.20
- Field percentile
- top 25%
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