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Mapping of H1 Cell Line MRE-Seq Data
Illumina reads produced by MRE-Seq on the H1 Cell Line, Library HS1153 were mapped to the human genome using Pash.
Project News:
2010/10/26: ANALYSIS XML file 'ucsf-ubc.mre.level.1.xml' uploaded
alias: HS1153-1_42F2TAAXX-HS1153-1_313MYAAXX-HS1153-1_42EMFAAXX.hg19.level.1
Analysis Center: EDACC Analysis File Type: .bed Analysis File Name: UCSF-UBC.H1.MRE-Seq.HS1153.bed DATA_ANALYSIS_LEVEL: 1 EXPERIMENT_TYPE: MRE-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: None ALIGNMENT_POSTPROCESSING: None RELEASE_NUMBER: Human Epigenome Atlas 2 NUMBER_OF_MRE-SEQ_EXPERIMENTS_SCORED: 28 PERCENT_READS_MAPPING_TO_RESTRICTION_FRAGMENTS: 89.07 PERCENT_READS_MAPPING_TO_RESTRICTION_FRAGMENTS_PERCENTILE: 7 |
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