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Mapping of Fetal Renal Pelvis Right Chromatin Accessibility Data
Illumina reads produced by DNAse-Seq on Fetal Renal Pelvis Right, Donor H-24169, Library DS18961 were mapped to the human genome using Pash.
Project News:
2012/5/3: ANALYSIS XML file 'uw.chromatin.accessibility.level.1.xml' uploaded
alias: DS18961.hg19.level.1.release.6
Analysis Center: EDACC Analysis File Type: .bed Analysis File Name: UW.Fetal_Renal_Pelvis_Right.ChromatinAccessibility.H-24169.DS18961.bed DATA_ANALYSIS_LEVEL: 1 EXPERIMENT_TYPE: Chromatin Accessibility GENOME_ASSEMBLY: NCBI Build GRCh37/UCSC Build hg19 SOFTWARE: Pash SOFTWARE_VERSION: 3.0 MAXIMUM_ALIGNMENT_LENGTH: Read length MISMATCHES_ALLOWED: 10% of read length ALIGNMENTS_ALLOWED: 1 TREATMENT_OF_MULTIPLE_ALIGNMENTS: If a read maps to more than 1 position it is removed from consideration. TREATMENT_OF_IDENTICAL_ALIGNMENTS_OF_MULTIPLE_READS: None ALIGNMENT_POSTPROCESSING: None RELEASE_NUMBER: Human Epigenome Atlas 6 NUMBER_OF_MAPPED_READS: 26,852,213 NUMBER_OF_CHROMATIN_ACCESSIBILITY_EXPERIMENTS_SCORED_IN_THIS_RELEASE: 63 FINDPEAKS_SCORE: 0.3824 FINDPEAKS_PERCENTILE: 52 HOTSPOT_SCORE: 0.3761 HOTSPOT_PERCENTILE: 52 IROC_SCORE: 0.9923 IROC_PERCENTILE: 38 POISSON_SCORE: 0.4452 POISSON_PERCENTILE: 51 MAXIMUM_REPLICATE_CORRELATION: 0.97 |
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