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Mapping of iPS DF 19.11 Cell Line ChIP-Seq Input Data
Illumina reads produced by ChIP-Seq Input on iPS DF 19.11 Cell Line, Library SK446, were mapped to the human genome using Pash.
Project News:
2011/11/21: ANALYSIS XML file 'ucsd.chip-seq.level.1.xml' uploaded
alias: renlab.Input.iPS-19.11.02.01.hg19.level.1.release.5
Analysis Center: EDACC Analysis File Type: .bed Analysis File Name: UCSD.iPS_DF_19.11.Input.SK446.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 5 NUMBER_OF_MAPPED_READS: 6,247,513 NUMBER_OF_Input_EXPERIMENTS_SCORED_IN_THIS_RELEASE: 61 FINDPEAKS_SCORE: 0.02 FINDPEAKS_PERCENTILE: 100 HOTSPOT_SCORE: 0.16 HOTSPOT_PERCENTILE: 100 IROC_SCORE: 0.61 IROC_PERCENTILE: 38 POISSON_SCORE: 0.32 POISSON_PERCENTILE: 100 MAXIMUM_REPLICATE_CORRELATION: 0.65 |
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