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File Set Type

Assay

8 items
IGVFDS3774FYIW
  • gary-hon:differentited_H9_CM_Pilot2_Mini_PB9_HTO_LW433
cell hashing barcode sequencing
preview
cell hashing barcode sequencing for CRISPR interference Perturb-seq integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci
IGVFDS3919NBFE
  • gary-hon:differentited_H9_CM_Pilot2_Mini_PB9_sgRNA_LW433
gRNA sequencing
preview
gRNA sequencing for CRISPR interference Perturb-seq integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci
IGVFDS1340IBKW
  • gary-hon:differentited_H9_CM_Pilot2_Mini_PB9_HTO_LW434
cell hashing barcode sequencing
preview
cell hashing barcode sequencing for CRISPR interference Perturb-seq integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci
IGVFDS1182KBMU
  • gary-hon:differentited_H9_CM_Pilot2_Mini_PB9_sgRNA_LW431
gRNA sequencing
preview
gRNA sequencing for CRISPR interference Perturb-seq integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci
IGVFDS0785CQUX
  • gary-hon:differentited_H9_CM_Pilot2_Mini_PB9_sgRNA_LW434
gRNA sequencing
preview
gRNA sequencing for CRISPR interference Perturb-seq integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci
IGVFDS6475OLUM
  • gary-hon:differentited_H9_CM_Pilot2_Mini_PB9_HTO_LW432
cell hashing barcode sequencing
preview
cell hashing barcode sequencing for CRISPR interference Perturb-seq integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci
IGVFDS5403GYDH
  • gary-hon:differentited_H9_CM_Pilot2_Mini_PB9_sgRNA_LW432
gRNA sequencing
preview
gRNA sequencing for CRISPR interference Perturb-seq integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci
IGVFDS2275IPCJ
  • gary-hon:differentited_H9_CM_Pilot2_Mini_PB9_HTO_LW431
cell hashing barcode sequencing
preview
cell hashing barcode sequencing for CRISPR interference Perturb-seq integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci