Published December 11, 2023
| Version v2
Dataset
Open
scSNV-seq data and code
Authors/Creators
- 1. Cellular and Gene Editing Research and Development, Wellcome Sanger Institute, Hinxton, Cambridge CB10 1SA, UK
- 2. Translational Cancer Genomics, Wellcome Sanger Institute, Hinxton, Cambridge, CB10 1SA, UK; Open Targets, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SD, UK
- 3. EMBL-European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SD, UK
- 4. Translational Cancer Genomics, Wellcome Sanger Institute, Hinxton, Cambridge, CB10 1SA, UK
- 5. EMBL-European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SD, UK;Cellular Genetics, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SD, UK;Cancer Research UK Cambridge Institute, University of Cambridge, Robinson Way, Cambridge, CB2 0RE, UK
- 6. Cellular and Gene Editing Research and Development, Wellcome Sanger Institute, Hinxton, Cambridge CB10 1SA, UK; Open Targets, Wellcome Genome Campus, Hinxton, Cambridge, CB10 1SD, UK
Description
Processed data and code from base editing and scSNV-seq experiments.
The code has been deposited on GitHub (https://github.com/MarioniLab/scSNV-seq).
Notes
This research was funded by the Wellcome Trust Grant 206194 and Open Targets (OTAR2061). M.S. is supported by the Wellcome Trust (220442/Z/20/Z).