|
|||||||||
Chromatin accessibility assay of Fetal Renal Pelvis
Chromatin accessibility determination via DNase-seq
Project News:
2011/3/31: EXPERIMENT XML file 'NREMC.experiment.chromatinAccessibility.DS17381.xml' uploaded
alias: DS17381
expected_number_runs: 1 center_name: NREMC STUDY_REF: UwStam_NREMC_CA SAMPLE_DESCRIPTOR: fKidney_renal_pelvis.H-23790d108 LIBRARY LIBRARY_NAME: DS17381 LIBRARY_STRATEGY: DNase-Hypersensitivity LIBRARY_SOURCE: GENOMIC LIBRARY_SELECTION: DNAse LIBRARY_LAYOUT: SINGLE POOLING_STRATEGY: other LIBRARY_CONSTRUCTION_PROTOCOL: Single read - Illumina SPOT NUMBER_OF_READS_PER_SPOT: READ_INDEX: 0 READ_CLASS: Application Read READ_TYPE: Forward BASE_COORD: 1 PLATFORM ILLUMINA INSTRUMENT_MODEL: Illumina Genome Analyzer IIx SEQUENCE_LENGTH: 36 BASE CALLS SCS v2.8 QUALITY SCORES SCS v2.8 ATTRIBUTES EXPERIMENT_TYPE: Chromatin Accessibility EXTRACTION_PROTOCOL: Qiagen minElut DNASE_PROTOCOL: Stamlab DNase Protocol, Sabo, P. J. et al. Nat Methods 3, 511?518 (2006) |
|||||||||
|
|||||||||