Showing 200 of 598 results
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- MPRA in WTC11Elements cloned into the lentiMPRA vector upstream of a minimal promoter, with barcode located in the 5' UTR of the reporter. Elements test neuronal enhancers and promoters.Lab: Nadav Ahituv, UCSFProject: ENCODE
- CRISPRi FACS screen in activated CD4-positive, CD25-positive, alpha-beta regulatory T cell with fluorescence activated cell sorting readout of Tnfrsf18Mus musculus strain Rosa26-LSL-dCas9-KRAB activated CD4-positive, CD25-positive, alpha-beta regulatory T cell genetically modified (CRISPRi) using CRISPRElements selection method: accessible genome regionsTiling modality: peak tilingLab: Tim Reddy, DukeProject: ENCODE
- CRISPRi screen in WTC11WTC11 cell line genetically modified (insertion) using transduction, genetically modified (CRISPRi) using CRISPRAssays: CRISPR screenLab: Bing Ren, UCSDProject: ENCODE
- proliferation CRISPR screen in DNA cloning sampleFunctional characterization series for tiling CRIPSRi proliferation screens at genome-wide cCREs essential for neuronal differentiationAssays: proliferation CRISPR screenLab: Yin Shen, UCSFProject: ENCODEElements selection method: accessible genome regions, histone modifications, essential genes
- MPRA in SK-N-SHHomo sapiens SK-N-SH, 24 hours post-nucleic acid delivery time genetically modified (episome) using transient transfectionLab: Ryan Tewhey, JAXProject: ENCODE
- MPRA in HepG2Homo sapiens HepG2, 24 hours post-nucleic acid delivery time genetically modified (episome) using transient transfectionLab: Ryan Tewhey, JAXProject: ENCODE
- MPRA in K562Homo sapiens K562, 24 hours post-nucleic acid delivery time genetically modified (episome) using transient transfectionLab: Ryan Tewhey, JAXProject: ENCODE
- MPRA in HepG2Homo sapiens HepG2, 24 hours post-nucleic acid delivery time genetically modified (episome) using transient transfectionLab: Ryan Tewhey, JAXProject: ENCODE
- MPRA in K562Homo sapiens K562, 24 hours post-nucleic acid delivery time genetically modified (episome) using transient transfectionLab: Ryan Tewhey, JAXProject: ENCODE
- MPRA in K562Homo sapiens K562, 24 hours post-nucleic acid delivery time genetically modified (episome) using transient transfectionLab: Ryan Tewhey, JAXProject: ENCODE
- MPRA in WTC11Elements cloned into the lentiMPRA vector upstream of a minimal promoter, with barcode located in the 5' UTR of the reporter. Elements test potential HepG2, K562, and WTC11 enhancers and promoters of all protein-coding genes.Lab: Nadav Ahituv, UCSFProject: ENCODE
- MPRA in HepG2Elements cloned into the lentiMPRA vector upstream of a minimal promoter, with barcode located in the 5' UTR of the reporter. Elements test potential HepG2, K562, and WTC11 enhancers and promoters of all protein-coding genes.Lab: Nadav Ahituv, UCSFProject: ENCODE
- MPRA in K562Elements cloned into the lentiMPRA vector upstream of a minimal promoter, with barcode located in the 5' UTR of the reporter. Elements test potential HepG2, K562, and WTC11 enhancers and promoters of all protein-coding genes.Lab: Nadav Ahituv, UCSFProject: ENCODE
- MPRA in WTC11Elements cloned into the lentiMPRA vector upstream of a minimal promoter, with barcode located in the 5' UTR of the reporter. Elements test potential WTC11 enhancers and promoters of protein-coding genes.Lab: Nadav Ahituv, UCSFProject: ENCODE
- STARR-seq in K562Homo sapiens K562 genetically modified (episome) using transient transfectionLab: Tim Reddy, DukeProject: ENCODE
- STARR-seq in glutamatergic neuronHomo sapiens glutamatergic neuron, 7 days post differentiation genetically modified (episome) using transient transfection, (insertion) using TALEN inserting M. musculus Neurog2Lab: Kevin White, UChicagoProject: ENCODE
- perturbation followed by snATAC-seq in K562K562 cell line genetically modified (insertion) using transduction, genetically modified (CRISPRi) using CRISPRAssays: perturbation followed by snATAC-seqLab: Will Greenleaf, StanfordProject: ENCODE
- CRISPR cutting screen of GATA1 locus in K562Homo sapiens K562 genetically modified (insertion) using transduction (low MOI), using CRISPR cutting (sgRNA) for GATA1 locus
- MPRA in HepG2Elements cloned into the lentiMPRA vector upstream of a minimal promoter, with barcode located in the 5' UTR of the reporter. Elements test HepG2 enhancers and promoters of all protein-coding genes.Elements selection method: synthetic elementsLab: Nadav Ahituv, UCSFProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- MPRA of SHH locus in NIH3T3Elements cloned into the pGL4Z vector upstream of a minimal promoter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the ZRS enhancer.
- MPRA of SHH locus in NIH3T3Elements cloned into the pGL4Z vector upstream of a minimal promoter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the ZRS enhancer.
- MPRA of ZFAND3 locus in MIN6Elements cloned into the pGL4.23 vector upstream of a minimal promoter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the ZFAND3 enhancer.
- MPRA in Neuro-2aElements cloned into the pGL4.23 vector upstream of a minimal promoter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the ultra conserved element UC88.Lab: Nadav Ahituv, UCSFProject: ENCODE
- MPRA of TERT locus in glial cellElements cloned into the pGL4.11 vector upstream of the reporter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the TERT promoter.
- MPRA of TERT locus in glial cellElements cloned into the pGL4.11 vector upstream of the reporter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the TERT promoter.
- MPRA of TERT locus in glial cellElements cloned into the pGL4.11 vector upstream of the reporter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the TERT promoter.
- MPRA of TERT locus in HEK293TElements cloned into the pGL4.11 vector upstream of the reporter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the TERT promoter.
- MPRA of TCF7L2 locus in MIN6Elements cloned into the pGL4.23 vector upstream of a minimal promoter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the TCF7L2 enhancer.
- MPRA of SORT1 locus in HepG2Elements cloned into the pGL4.23 vector upstream of a minimal promoter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the SORT enhancer, using 3' to 5' direction.
- MPRA of SORT1 locus in HepG2Elements cloned into the pGL4.23 vector upstream of a minimal promoter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the SORT1 enhancer.
- MPRA of SORT1 locus in HepG2Elements cloned into the pGL4.23 vector upstream of a minimal promoter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the SORT1 enhancer.
- MPRA of RET locus in Neuro-2aElements cloned into the pGL3 vector upstream of a minimal promoter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the RET enhancer.
- MPRA of PKLR locus in K562Elements cloned into the pGL4.11 vector upstream of the reporter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the PKLR promoter.
- MPRA of PKLR locus in K562Elements cloned into the pGL4.11 vector upstream of the reporter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the PKLR promoter.
- MPRA of MYC locus in HEK293TElements cloned into the pGL4.23 vector upstream of a minimal promoter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the MYC enhancer around SNP rs6983267.
- MPRA of MYC locus in LNCAPElements cloned into the pGL4.23 vector upstream of a minimal promoter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the MYC enhancer around SNP rs11986220.
- MPRA of MSMB locus in HEK293TElements cloned into the pGL4.11 vector upstream of the reporter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the MSMB promoter.
- MPRA of LDLR locus in HepG2Elements cloned into the pGL4.11 vector upstream of the reporter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the LDLR promoter.
- MPRA of LDLR locus in HepG2Elements cloned into the pGL4.11 vector upstream of the reporter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the LDLR promoter.
- MPRA of IRF6 locus in HaCaTElements cloned into the pGL4.23 vector upstream of a minimal promoter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the IRF6 enhancer.
- MPRA of IRF4 locus in SK-MEL-28Elements cloned into the pGL4.23 vector upstream of a minimal promoter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the IRF4 enhancer.
- MPRA of HNF4A locus in HEK293TElements cloned into the pGL4.11 vector upstream of the reporter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the HNF4A promoter.
- MPRA of HBG1 locus in HELElements cloned into the pGL4.11 vector upstream of the reporter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the HBG1 promoter.
- MPRA of HBB locus in HELElements cloned into the pGL4.11 vector upstream of the reporter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the HBB promoter.
- MPRA of GP1BB locus in HELElements cloned into the pGL4.11 vector upstream of the reporter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the GP1BB promoter.
- MPRA of FOXE1 locus in HeLaElements cloned into the pGL4.11 vector upstream of the reporter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the FOXE1 promoter.
- MPRA of F9 locus in HepG2Elements cloned into the pGL4.11 vector upstream of the reporter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the F9 promoter.
- MPRA of BCL11A locus in HELElements cloned into the pGL4.23 vector upstream of a minimal promoter, with barcode located in the 3' UTR of the reporter. Elementas are generated by error-prone PCR of the BCL11A enhancer.
- CRISPR cutting FACS screen of Sox2 locus in F123 with endogenous protein Sort-seq readout of Sox2Mus musculus F123 genetically modified (insertion) using transduction, using CRISPR cutting (sgRNA) for Sox2 locus
- CRISPR cutting FACS screen of Esrrb locus in F123 with endogenous protein Sort-seq readout of EsrrbMus musculus F123 genetically modified (insertion) using transduction, using CRISPR cutting (sgRNA) for Esrrb locus
- CRISPR cutting FACS screen of Dppa2 locus in F123 with endogenous protein Sort-seq readout of Dppa2Mus musculus F123 genetically modified (insertion) using transduction, using CRISPR cutting (sgRNA) for Dppa2 locus
- MPRA in DNA cloning sampleThese MPRA datasets test a mix of short, medium, and long elements cloned into the pGL4 vector upstream of a minimal promoter.Assays: MPRALab: Nadav Ahituv, UCSFProject: ENCODEElements selection method: DNase hypersensitive sites
- MPRA in DNA cloning sampleThese MPRA datasets test the same set of elements cloned into the pGL4 vector upstream of a minimal promoter in both the forward and reverse orientations in parallel.Assays: MPRALab: Nadav Ahituv, UCSFProject: ENCODEElements selection method: DNase hypersensitive sites
- MPRA in DNA cloning sampleThese MPRA datasets screen a library of 2,440 candidate liver enhancers and controls for regulatory activity in HepG2 cells using nine different MPRA designs.Assays: MPRALab: Nadav Ahituv, UCSFProject: ENCODEElements selection method: DNase hypersensitive sites
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- enhancer reporter assay in whole organismstrain FVB/NCrl whole organism embryo (11.5 days) genetically modified (insertion) using mouse pronuclear microinjectionLab: Len Pennacchio, LBNLProject: ENCODE
- CRISPRi proliferation screen of multiple loci in WTC11Homo sapiens WTC11 genetically modified (insertion) using transduction, using CRISPRi (sgRNA) for multiple loci
- CRISPR cutting proliferation screen of multiple loci in WTC11Homo sapiens WTC11 genetically modified (insertion) using transduction, using CRISPR cutting (sgRNA) for multiple loci
- CRISPRi proliferation screen of multiple loci in PC-3Homo sapiens PC-3 genetically modified (insertion) using transduction, using CRISPRi (pgRNA) for multiple loci
- CRISPRi proliferation screen of multiple loci in DU 145Homo sapiens DU 145 genetically modified (insertion) using transduction, using CRISPRi (pgRNA) for multiple loci
- CRISPRi proliferation screen of multiple loci in NCI-H460Homo sapiens NCI-H460 genetically modified (insertion) using transduction, using CRISPRi (pgRNA) for multiple loci
- CRISPRi proliferation screen of multiple loci in A549Homo sapiens A549 genetically modified (insertion) using transduction, using CRISPRi (pgRNA) for multiple loci
- CRISPRi proliferation screen of multiple loci in MDA-MB-231Homo sapiens MDA-MB-231 genetically modified (insertion) using transduction, using CRISPRi (pgRNA) for multiple loci
- CRISPRi proliferation screen of multiple loci in MCF-7Homo sapiens MCF-7 genetically modified (insertion) using transduction, using CRISPRi (pgRNA) for multiple loci
- CRISPRi proliferation screen of multiple loci in HepG2Homo sapiens HepG2 genetically modified (insertion) using transduction, using CRISPRi (pgRNA) for multiple loci
- CRISPRi proliferation screen of multiple loci in SW620Homo sapiens SW620 genetically modified (insertion) using transduction, using CRISPRi (pgRNA) for multiple loci
- CRISPRi proliferation screen of multiple loci in HCT116Homo sapiens HCT116 genetically modified (insertion) using transduction, using CRISPRi (pgRNA) for multiple loci
- CRISPRi proliferation screen of multiple loci in K562Homo sapiens K562 genetically modified (insertion) using transduction, using CRISPRi (pgRNA) for multiple loci
- MPRA in K562Homo sapiens K562, 24 hours post-nucleic acid delivery time genetically modified (episome) using transient transfectionElements selection method: sequence variantsLab: Ryan Tewhey, JAXProject: ENCODE
- CRISPRi proliferation screen in OCI-AML2Functional characterization series of CRISPRi (dCas9-KRAB) growth screen targeting putative essential DHSs in K562. (validation screen in OCI-AML2).Assays: proliferation CRISPR screenLab: Tim Reddy, DukeProject: ENCODETiling modality: sparse peak
- CRISPRi proliferation screen in K562Functional characterization series of CRISPRi (dCas9-KRAB) growth screen targeting putative essential DHSs in K562 .(validation screen in K562).Assays: proliferation CRISPR screenLab: Tim Reddy, DukeProject: ENCODETiling modality: sparse peak
- CRISPRi proliferation screen in K562Functional characterization series of CRISPRi (dCas9-KRAB) growth screen targeting all previously identified open chromatin regions (DHSs) in K562. (Discovery screen).Assays: proliferation CRISPR screenLab: Tim Reddy, DukeProject: ENCODETiling modality: peak tiling
- CRISPRi Flow-FISH screen in K562 with HCR-FlowFISH readout of HBS1LFunctional characterization series for the gene target HBS1L.Assays: Flow-FISH CRISPR screenLab: Pardis Sabeti, BroadProject: ENCODETiling modality: full tiling
- CRISPRi Flow-FISH screen in K562 with HCR-FlowFISH readout of MYBFunctional characterization series for the gene target MYB.Assays: Flow-FISH CRISPR screenLab: Pardis Sabeti, BroadProject: ENCODETiling modality: full tiling
- CRISPRi Flow-FISH screen in K562 with HCR-FlowFISH readout of HBE1Functional characterization series for the gene target HBE1.Assays: Flow-FISH CRISPR screenLab: Pardis Sabeti, BroadProject: ENCODETiling modality: full tiling
- CRISPRi Flow-FISH screen in K562 with HCR-FlowFISH readout of HBG2Functional characterization series for the gene target HBG2.Assays: Flow-FISH CRISPR screenLab: Pardis Sabeti, BroadProject: ENCODETiling modality: full tiling
- CRISPRi Flow-FISH screen in K562 with HCR-FlowFISH readout of HBG1Functional characterization series for the gene target HBG1.Assays: Flow-FISH CRISPR screenLab: Pardis Sabeti, BroadProject: ENCODETiling modality: full tiling
- CRISPRi proliferation screen in K562Functional characterization series for CRISPRi/dCas9-RYBP sparse-tiling proliferation screens at ~7500 cCREs around ~450 essential genes in K562Assays: proliferation CRISPR screenLab: Will Greenleaf, StanfordProject: ENCODEElements selection method: DNase hypersensitive sitesTiling modality: sparse peak
- CRISPRi proliferation screen in K562Functional characterization series for CRISPRi/dCas9-KRAB-WSR7EEE sparse-tiling proliferation screens at ~7500 cCREs around ~450 essential genes in K562Assays: proliferation CRISPR screenLab: Will Greenleaf, StanfordProject: ENCODEElements selection method: DNase hypersensitive sitesTiling modality: sparse peak
- CRISPRi proliferation screen in K562Functional characterization series for CRISPRi/dCas9-KRAB-MGA1-MGA2 sparse-tiling proliferation screens at ~7500 cCREs around ~450 essential genes in K562Assays: proliferation CRISPR screenLab: Will Greenleaf, StanfordProject: ENCODEElements selection method: DNase hypersensitive sitesTiling modality: sparse peak
- CRISPRi proliferation screen in K562Functional characterization series for dCas9-ZNF705-KRAB/CRISPRi tiling proliferation screens at a subset of cCREs around essential genesAssays: proliferation CRISPR screenLab: Will Greenleaf, StanfordProject: ENCODEElements selection method: DNase hypersensitive sitesTiling modality: peak tiling
- CRISPRi proliferation screen in K562Functional characterization series for dCas9-RYBP/CRISPRi tiling proliferation screens at a subset of cCREs around essential genesAssays: proliferation CRISPR screenLab: Will Greenleaf, StanfordProject: ENCODEElements selection method: DNase hypersensitive sitesTiling modality: peak tiling
- CRISPRi proliferation screen in K562Functional characterization series for dCas9-KRAB-WSR7EEE/CRISPRi tiling proliferation screens at a subset of cCREs around essential genesAssays: proliferation CRISPR screenLab: Will Greenleaf, StanfordProject: ENCODEElements selection method: DNase hypersensitive sitesTiling modality: peak tiling
- CRISPRi proliferation screen in K562Functional characterization series for dCas9-KRAB/CRISPRi tiling proliferation screens at a subset of cCREs around essential genesAssays: proliferation CRISPR screenLab: Will Greenleaf, StanfordProject: ENCODEElements selection method: DNase hypersensitive sitesTiling modality: peak tiling
- CRISPR dCas proliferation screen in K562Functional characterization series for dCas9 tiling proliferation screens at a subset of cCREs around essential genesAssays: proliferation CRISPR screenLab: Will Greenleaf, StanfordProject: ENCODEElements selection method: DNase hypersensitive sitesTiling modality: peak tiling
- CRISPR cutting proliferation screen of CTCF locus in K562Functional characterization series for Cas9/CRISPR fine-mapping proliferation screens at hit and non-hit CTCF motifs in loop anchors (and their partner anchors) from the CTCF growth screenAssays: proliferation CRISPR screenLab: Will Greenleaf, StanfordProject: ENCODEElements selection method: TF binding sitesLoci: CTCFTiling modality: peak tiling
- CRISPR dCas proliferation screen of CTCF locus in K562Functional characterization series for dCas9/CRISPRd proliferation screens at CTCF motifs in loop anchorsAssays: proliferation CRISPR screenLab: Will Greenleaf, StanfordProject: ENCODEElements selection method: TF binding sitesLoci: CTCFTiling modality: sparse peak
- CRISPRa proliferation screen of CTCF locus in K562Functional characterization series for dCas9-VPR/CRISPRa proliferation screens at CTCF motifs in loop anchorsAssays: proliferation CRISPR screenLab: Will Greenleaf, StanfordProject: ENCODEElements selection method: TF binding sitesLoci: CTCFTiling modality: sparse peak
- CRISPR cutting proliferation screen of CTCF locus in K562Functional characterization series for Cas9/CRISPRk proliferation screens at CTCF motifs in loop anchorsAssays: proliferation CRISPR screenLab: Will Greenleaf, StanfordProject: ENCODEElements selection method: TF binding sitesLoci: CTCFTiling modality: sparse peak
- CRISPRi proliferation screen of CTCF locus in K562Functional characterization series for dCas9-KRAB/CRISPRi proliferation screens at CTCF motifs in loop anchorsAssays: proliferation CRISPR screenLab: Will Greenleaf, StanfordProject: ENCODEElements selection method: TF binding sitesLoci: CTCFTiling modality: sparse peak
- STARR-seq in K562Homo sapiens K562 genetically modified (episome) using transient transfectionElements selection method: accessible genome regionsLab: Tim Reddy, DukeProject: ENCODE
- STARR-seq in activated T-helper 17 cellMus musculus strain C57BL/6NJ activated T-helper 17 cell genetically modified (episome) using transient transfectionElements selection method: accessible genome regionsLab: Tim Reddy, DukeProject: ENCODE
- STARR-seq in glutamatergic neuronHomo sapiens glutamatergic neuron, 14 days post differentiation genetically modified (episome) using transient transfection, (insertion) using TALEN inserting M. musculus Neurog2 originated from WTC11Lab: Kevin White, UChicagoProject: ENCODE
- STARR-seq in WTC11Homo sapiens WTC11 genetically modified (episome) using transient transfection, (insertion) using TALEN inserting M. musculus Neurog2Lab: Kevin White, UChicagoProject: ENCODE
- STARR-seq in activated CD4-positive, CD25-positive, alpha-beta regulatory T cellMus musculus strain C57BL/6NJ activated CD4-positive, CD25-positive, alpha-beta regulatory T cell genetically modified (episome) using transient transfectionElements selection method: accessible genome regionsLab: Tim Reddy, DukeProject: ENCODE
- STARR-seq in activated T-helper 17 cellMus musculus strain C57BL/6NJ activated T-helper 17 cell genetically modified (episome) using transient transfectionElements selection method: accessible genome regionsLab: Tim Reddy, DukeProject: ENCODE
- STARR-seq in activated T-helper 2 cellMus musculus strain C57BL/6NJ activated T-helper 2 cell genetically modified (episome) using transient transfectionElements selection method: accessible genome regionsLab: Tim Reddy, DukeProject: ENCODE
- STARR-seq in activated T-helper 1 cellMus musculus strain C57BL/6NJ activated T-helper 1 cell genetically modified (episome) using transient transfectionElements selection method: accessible genome regionsLab: Tim Reddy, DukeProject: ENCODE
- STARR-seq in activated naive CD4-positive, alpha-beta T cellMus musculus strain C57BL/6NJ activated naive CD4-positive, alpha-beta T cell genetically modified (episome) using transient transfectionElements selection method: accessible genome regionsLab: Tim Reddy, DukeProject: ENCODE
- CRISPR dCas proliferation screen of multiple loci in K562Functional characterization series for tiling, dCas9/CRISPRd proliferation screens at the GATA1 locus
- CRISPRa proliferation screen of multiple loci in K562Functional characterization series for tiling, dCas9-VPR/CRISPRa proliferation screens at the GATA1 locus
- CRISPR cutting proliferation screen of multiple loci in K562Functional characterization series for tiling, Cas9/CRISPRk proliferation screens at the GATA1 locus
- CRISPRi proliferation screen of multiple loci in K562Functional characterization series for tiling, dCas9-KRAB/CRISPRi proliferation screens at the GATA1 locus
- CRISPR cutting proliferation screen of MYC locus in K562Homo sapiens K562 genetically modified (insertion) using transduction (low MOI), using CRISPR cutting (sgRNA) for MYC locusAssays: proliferation CRISPR screenLab: Yin Shen, UCSFProject: ENCODELoci: MYCTiling modality: peak tiling
- CRISPR cutting proliferation screen of GATA1 locus in K562Homo sapiens K562 genetically modified (insertion) using transduction (low MOI), using CRISPR cutting (sgRNA) for GATA1 locusAssays: proliferation CRISPR screenLab: Yin Shen, UCSFProject: ENCODELoci: GATA1Tiling modality: peak tiling
- STARR-seq in pancreas organoidHomo sapiens organoid with pancreatic ductal adenocarcinoma; pancreas genetically modified (episome) using transient transfectionElements selection method: accessible genome regions, histone modificationsLab: Kevin White, UChicagoProject: ENCODE
- STARR-seq in pancreas organoidHomo sapiens organoid with pancreatic ductal adenocarcinoma; pancreas genetically modified (episome) using transient transfectionElements selection method: accessible genome regions, histone modifications, DNase hypersensitive sitesLab: Kevin White, UChicagoProject: ENCODE
- STARR-seq in pancreas organoidHomo sapiens organoid with pancreatic ductal adenocarcinoma; pancreas genetically modified (episome) using transient transfectionElements selection method: accessible genome regions, histone modificationsLab: Kevin White, UChicagoProject: ENCODE
- STARR-seq in pancreas organoidHomo sapiens organoid with pancreatic ductal adenocarcinoma; pancreas genetically modified (episome) using transient transfectionElements selection method: accessible genome regions, histone modifications, DNase hypersensitive sitesLab: Kevin White, UChicagoProject: ENCODE
- CRISPRi proliferation screen in K562K562 cell line genetically modified (insertion) using transduction, genetically modified (CRISPRi) using CRISPRAssays: proliferation CRISPR screenLab: Bing Ren, UCSDProject: ENCODEElements selection method: histone modificationsTiling modality: peak tiling
- CRISPRi proliferation screen in HCT116HCT116 cell line genetically modified (insertion) using transduction, genetically modified (CRISPRi) using CRISPRAssays: proliferation CRISPR screenLab: Bing Ren, UCSDProject: ENCODEElements selection method: histone modificationsTiling modality: peak tiling
- CRISPR cutting FACS screen of Sox2 locus in F123 with endogenous protein Sort-seq readout of Sox2Mus musculus F123 genetically modified (insertion) using CRISPR (sgRNA) targeting M. musculus Sox2, (insertion) using transduction, using CRISPR cutting (sgRNA) for Sox2 locusAssays: FACS CRISPR screenLab: Yin Shen, UCSFProject: ENCODEElements selection method: DNase hypersensitive sitesLoci: Sox2Tiling modality: peak tiling
- CRISPR cutting FACS screen of SIN3A locus in glutamatergic neuron with endogenous protein Sort-seq readout of SIN3AHomo sapiens glutamatergic neuron genetically modified (insertion) using CRISPR (pgRNA) targeting H. sapiens SIN3A, (insertion) using transduction, using CRISPR cutting (pgRNA) for SIN3A locus
- CRISPR cutting FACS screen of SIN3A locus in WTC11 with endogenous protein Sort-seq readout of SIN3AHomo sapiens WTC11 genetically modified (insertion) using CRISPR (pgRNA) targeting H. sapiens SIN3A, (insertion) using transduction, using CRISPR cutting (pgRNA) for SIN3A locus
- CRISPR cutting FACS screen of APP locus in glutamatergic neuron with endogenous protein Sort-seq readout of APPHomo sapiens glutamatergic neuron genetically modified (insertion) using CRISPR (pgRNA) targeting H. sapiens APP, (insertion) using transduction, using CRISPR cutting (pgRNA) for APP locus
- CRISPR cutting FACS screen of SIN3A locus in glutamatergic neuron with endogenous protein Sort-seq readout of SIN3AHomo sapiens glutamatergic neuron genetically modified (insertion) using CRISPR (pgRNA) targeting H. sapiens SIN3A, (insertion) using transduction, using CRISPR cutting (pgRNA) for SIN3A locus
- CRISPR cutting FACS screen of Esrrb locus in F123 with endogenous protein Sort-seq readout of EsrrbMus musculus F123 genetically modified (insertion) using CRISPR (sgRNA) targeting M. musculus Esrrb, (insertion) using transduction, using CRISPR cutting (sgRNA) for Esrrb locusAssays: FACS CRISPR screenLab: Yin Shen, UCSFProject: ENCODEElements selection method: DNase hypersensitive sitesLoci: EsrrbTiling modality: peak tiling
- CRISPR cutting FACS screen of Dppa2 locus in F123 with endogenous protein Sort-seq readout of Dppa2Mus musculus F123 genetically modified (insertion) using CRISPR (sgRNA) targeting M. musculus Dppa2, (insertion) using transduction, using CRISPR cutting (sgRNA) for Dppa2 locusAssays: FACS CRISPR screenLab: Yin Shen, UCSFProject: ENCODEElements selection method: DNase hypersensitive sitesLoci: Dppa2Tiling modality: peak tiling
- CRISPR cutting FACS screen of MECP2 locus in glutamatergic neuron with endogenous protein Sort-seq readout of MECP2Homo sapiens glutamatergic neuron genetically modified (insertion) using CRISPR (pgRNA) targeting H. sapiens MECP2, (insertion) using transduction, using CRISPR cutting (pgRNA) for MECP2 locus
- CRISPR cutting FACS screen of FMR1 locus in glutamatergic neuron with endogenous protein Sort-seq readout of FMR1glutamatergic neuron in vitro differentiated cells genetically modified (insertion) using transduction, genetically modified (insertion) using CRISPR targeting H. sapiens FMR1, genetically modified (CRISPR cutting) using CRISPR for FMR1 locus,
- CRISPR cutting FACS screen of Esrrb locus in F123 with endogenous protein Sort-seq readout of EsrrbMus musculus F123 genetically modified (insertion) using transduction, using CRISPR cutting (sgRNA) for Esrrb locus
- CRISPR cutting FACS screen of APP locus in WTC11 with endogenous protein Sort-seq readout of APPHomo sapiens WTC11 genetically modified (insertion) using CRISPR (pgRNA) targeting H. sapiens APP, (insertion) using transduction, using CRISPR cutting (pgRNA) for APP locus
- CRISPR cutting FACS screen of APP locus in glutamatergic neuron with endogenous protein Sort-seq readout of APPHomo sapiens glutamatergic neuron genetically modified (insertion) using CRISPR (pgRNA) targeting H. sapiens APP, (insertion) using transduction, using CRISPR cutting (pgRNA) for APP locus
- CRISPR cutting FACS screen of Esrrb locus in F123 with endogenous protein Sort-seq readout of EsrrbMus musculus F123 genetically modified (insertion) using CRISPR (sgRNA) targeting M. musculus Esrrb, (insertion) using transduction, using CRISPR cutting (sgRNA) for Esrrb locusAssays: FACS CRISPR screenLab: Yin Shen, UCSFProject: ENCODEElements selection method: DNase hypersensitive sitesLoci: EsrrbTiling modality: peak tiling
- CRISPR cutting FACS screen of Dppa2 locus in F123 with endogenous protein Sort-seq readout of Dppa2Mus musculus F123 genetically modified (insertion) using transduction, using CRISPR cutting (sgRNA) for Dppa2 locus
- CRISPR cutting FACS screen of APP locus in WTC11 with endogenous protein Sort-seq readout of APPHomo sapiens WTC11 genetically modified (insertion) using CRISPR (pgRNA) targeting H. sapiens APP, (insertion) using transduction, using CRISPR cutting (pgRNA) for APP locus