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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 'BI.H1.analysis.chipSeq.xml' uploaded
alias: BI.H1.INPUT.Level1.1
Analysis Center: EDACC
Experiment Refname: 314G6AAXX090406-5-S
Analysis File Type: .bam
Analysis File Name: BI.H1.input.FC_314G6AAXX_ln_5.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
Analysis Center: EDACC
Experiment Refname: 314G6AAXX090406-5-S
Analysis File Type: .bam
Analysis File Name: BI.H1.input.FC_314G6AAXX_ln_5.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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