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Mapping of Bladder Input ChIP-Seq Data
Illumina reads produced by Input ChIP-Seq on Bladder, Donor STL003, were mapped to the human genome using Pash.
Project News:
2013/6/10: ANALYSIS XML file 'ucsd.chip-seq.level.1.xml' uploaded
alias: renlab.Input.STL003BL.02.01-renlab.Input.STL003BL.01.01.hg19.level.1.release.9
Analysis Center: EDACC Analysis File Type: .bed Analysis File Name: UCSD.Bladder.Input.STL003.CY49.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: 25,221,478 FINDPEAKS_SCORE: 0.01 FINDPEAKS_PERCENTILE: 93 HOTSPOT_SCORE: 0.02 HOTSPOT_PERCENTILE: 59 IROC_SCORE: 0.9677 IROC_PERCENTILE: 60 POISSON_SCORE: 0.07 POISSON_PERCENTILE: 52 MAXIMUM_REPLICATE_CORRELATION: 0.98 |
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