CRISPR-Cas Systems for RNA and Genome Editing Part A

1. Massively parallel genomic perturbations with multi-target CRISPR interrogates Cas9 activity and DNA repair at endogenous sites
TJ Ha

2. Genome oligopaint via local denaturation fluorescence in situ hybridization
TJ Ha

3. TBD
Osamu Nureki

4. Biochemical reconstitution of a type I-B CRISPR-associated transposon
Leifu Chang

5. TBD
Yibei Xiao

6. Visualising the conformational landscape of of CRISPR-Cas9 through kinetics-informed structural studies
David W. Taylor

7. Analysis of metal-dependent DNA nicking activities by Cas endonucleases
Dipali G. Sashital

8. Biochemically characterizing the accessory proteins and ribonucleoprotein complexes of Type IV CRISPR systems.
Ryan Jackson

9. HYER
Junjie (Gogo) liu

10. focused on the purification and characterization of gRAMP, as well as its application in GFP knockdown in E. coli.
Chunyi Hu

11. TBD
Peter Fineran

12. Cas12a2 ?
Chase Beisel

13. Prime editing in bacteria with BacPE
Quanjiang Ji

14. TBD
Jia Chen

15. Preparation of high-purity CRISPR-based DNA base editor RNPs
Audrone Lapinaite

16. Bacterial directed evolution of CRISPR base editors
Shannon Miller

17. Cloning and validating systems for high throughput molecular recording
Michelle Chan

18. TBD
Samagya Banskota

19. Using CRISPR-Cas13 for viral nucleic acid detection
Cameron Myhrvold

20. CRISPR-based epigenetic editing for programmable gene silencing in mammalian cells
James Nuñez

21. Genome editing with programmable base editors in human cells” – explaining how to pick out and validate BE:gRNA combinations for a given target, with tips and tricks for maximizing editing efficiencies
Alexis Komor

22. High-throughput evaluation of genetic variants using base/prime editing sensor libraries
Francisco J. Sánchez Rivera

23. TBD
Jia Chen