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Mapping of Peripheral Blood Mononuclear Primary Cells Input ChIP-Seq Data
Illumina reads produced by Input ChIP-Seq on Peripheral Blood Mononuclear Primary Cells, Donor TC015, Library A21632 were mapped to the human genome using Pash.
Project News:
2013/6/13: ANALYSIS XML file 'ucsf-ubc.chip-seq.level.1.xml' uploaded
alias: A21632-1.hg19.level.1.release.9
Analysis Center: EDACC Analysis File Type: .bed Analysis File Name: UCSF-UBC.Peripheral_Blood_Mononuclear_Primary_Cells.Input.TC015.bed DATA_ANALYSIS_LEVEL: 1 EXPERIMENT_TYPE: ChIP-Seq 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: If multiple reads map to the same start position on the + strand or stop position on the - strand, only a single read is retained. ALIGNMENT_POSTPROCESSING: None READ_EXTENSION: 200bp RELEASE_NUMBER: Human Epigenome Atlas 9 NUMBER_OF_MAPPED_READS: 24,367,081 FINDPEAKS_SCORE: 0.0064 FINDPEAKS_PERCENTILE: 69 HOTSPOT_SCORE: 0.0075 HOTSPOT_PERCENTILE: 40 IROC_SCORE: 0.9733 IROC_PERCENTILE: 68 POISSON_SCORE: 0.0305 POISSON_PERCENTILE: 28 MAXIMUM_REPLICATE_CORRELATION: 0.99 |
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