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Chromatin accessibility assay of Fetal Heart Tissue
Chromatin accessibility determination via DNase-seq


Project News:
2011/1/23:
EXPERIMENT XML file 'NREMC.experiment.chromatinAccessibility.DS15839.xml' uploaded



alias: DS15839
expected_number_runs: 3
center_name: NREMC

STUDY_REF: UwStam_NREMC_CA
SAMPLE_DESCRIPTOR: fHeart.H-23468d96

LIBRARY
LIBRARY_NAME: DS15839
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)

 

 


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