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Mapping of IMR90 Chromatin Accessibility Data
Illumina reads produced by DNAse-Seq on the IMR90 cell line were mapped to the human genome (NCBI Build 36.1) using Pash.
Project News:
2009/12/18: ANALYSIS XML file 'UW.IMR90.analysis.chromatinAccessibility.xml' uploaded
alias: UW.IMR90.ChromatinAccessibility.Level1.3
Analysis Center: EDACC Experiment Refname: DS11764 Analysis File Type: .bam Analysis File Name: UW.IMR90.rep2.ChromatinAccessibility.IMR90-DS11764.UWStam_090902_SOLEXA-1GA-1_0021_FC42KVW_3.bam DATA_ANALYSIS_LEVEL: 1 EXPERIMENT_TYPE: Chromatin Accessibility 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 |
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