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Mapping of H1 Cell Line mRNA-Seq Data
Illumina reads produced by mRNA-Seq on the H1 Cell Line, Library H1EScd1 batch2 vial2 were mapped to the human genome using Pash.
Project News:
2010/10/28: ANALYSIS XML file 'ucsf-ubc.mrna-seq.level.1.xml' uploaded
alias: HS1272-1_612FTAAXX-HS1272-1_42VR1AAXX.hg19.level.1
Analysis Center: EDACC Analysis File Type: .bed Analysis File Name: UCSF-UBC.H1.mRNA-Seq.H1EScd1_batch2_vial2.bed DATA_ANALYSIS_LEVEL: 1 EXPERIMENT_TYPE: mRNA-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_MRNA-SEQ_EXPERIMENTS_SCORED: 4 PERCENT_READS_MAPPING_TO_UCSC_GENES: 89.50 PERCENT_READS_MAPPING_TO_UCSC_GENES_PERCENTILE: 25 |
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