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Mapping of H1 Input ChIP-Seq Data
Illumina reads produced as ChIP-Seq Input from the H1 cell line were mapped to the human genome (NCBI Build 36.1) using Pash.
Project News:
2009/12/11: ANALYSIS XML file 'ucsf-ubc.analysis.input.xml' uploaded
alias: UCSF-UBC.INPUT.Level1.2
Analysis Center: EDACC Experiment Refname: HS1028-1_3061PAAXX Analysis File Type: .bam Analysis File Name: UCSF-UBC.input.2.bam DATA_ANALYSIS_LEVEL: 1 EXPERIMENT_TYPE: ChIP-Seq 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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