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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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