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fastq
4
yaml
4
Content Type
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reads
4
seqspec
4
file_set.@id
/auxiliary-sets/IGVFDS9328UUVN/
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8 items
ConfigurationFile
IGVFFI9000DITZ
yaml - seqspec
Jesse Engreitz, Stanford
File Set
gRNA sequencing for mixed CRISPR FlowFISH screen integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci
Seqspec Of
IGVFFI8430IXFV
released
validated
SequenceFile
IGVFFI8181DYGV
fastq - reads
Jesse Engreitz, Stanford
File Set
gRNA sequencing for mixed CRISPR FlowFISH screen integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci
released
validated
SequenceFile
IGVFFI8430IXFV
fastq - reads
Jesse Engreitz, Stanford
File Set
gRNA sequencing for mixed CRISPR FlowFISH screen integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci
released
validated
SequenceFile
IGVFFI8166TMOU
fastq - reads
Jesse Engreitz, Stanford
File Set
gRNA sequencing for mixed CRISPR FlowFISH screen integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci
released
validated
ConfigurationFile
IGVFFI4656ZGKK
yaml - seqspec
Jesse Engreitz, Stanford
File Set
gRNA sequencing for mixed CRISPR FlowFISH screen integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci
Seqspec Of
IGVFFI8181DYGV
released
validated
ConfigurationFile
IGVFFI7169ITED
yaml - seqspec
Jesse Engreitz, Stanford
File Set
gRNA sequencing for mixed CRISPR FlowFISH screen integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci
Seqspec Of
IGVFFI8480BRGG
released
validated
ConfigurationFile
IGVFFI0106NXXW
yaml - seqspec
Jesse Engreitz, Stanford
File Set
gRNA sequencing for mixed CRISPR FlowFISH screen integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci
Seqspec Of
IGVFFI8166TMOU
released
validated
SequenceFile
IGVFFI8480BRGG
fastq - reads
Jesse Engreitz, Stanford
File Set
gRNA sequencing for mixed CRISPR FlowFISH screen integrating a guide (sgRNA) library targeting accessible genome regions in many genomic loci
released
validated