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Mapping of CD8 Naive Primary Cells ChIP-Seq Input Data
Illumina reads produced by ChIP-Seq Input on CD8 Naive Primary Cells, Donor TC001 were mapped to the human genome using Pash.


Project News:
2010/11/1:
ANALYSIS XML file 'ucsf-ubc.chip-seq.level.1.xml' uploaded



alias: HS2284-1_61LH3AAXX.hg19.level.1
Analysis Center: EDACC
Analysis File Type: .bed
Analysis File Name: UCSF-UBC.CD8_Naive_Primary_Cells.Input.TC001.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: 10
TREATMENT_OF_MULTIPLE_ALIGNMENTS: If a read maps to more than 10 positions 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 2
NUMBER_OF_Input_EXPERIMENTS_SCORED: 67
FINDPEAKS_SCORE: 0.0093
FINDPEAKS_PERCENTILE: 43
HOTSPOT_SCORE: 0.0211
HOTSPOT_PERCENTILE: 35
IROC_SCORE: 0.9369
IROC_PERCENTILE: 69
POISSON_SCORE: 0.2339
POISSON_PERCENTILE: 46

 

 


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