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Mapping of H1 Cell Line mRNA-Seq Data
Illumina reads produced by mRNA-Seq on the H1 Cell Line, Library polyA-RNA-seq_h1_r2a were mapped to the human genome using Pash.
Project News:
2012/8/29: ANALYSIS XML file 'ucsd.mrna-seq.level.1.xml' uploaded
alias: polyA-RNA-seq_h1_r2a.hg19.level.1.release.8
Analysis Center: EDACC Analysis File Type: .bed Analysis File Name: UCSD.H1.mRNA-Seq.polyA-RNA-seq_h1_r2a.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: 1 TREATMENT_OF_MULTIPLE_ALIGNMENTS: If a read maps to more than 1 position it is removed from consideration. TREATMENT_OF_IDENTICAL_ALIGNMENTS_OF_MULTIPLE_READS: None ALIGNMENT_POSTPROCESSING: None RELEASE_NUMBER: Human Epigenome Atlas 8 NUMBER_OF_MAPPED_READS: 327,201,303 NUMBER_OF_MRNA-SEQ_EXPERIMENTS_SCORED_IN_THIS_RELEASE: 22 PERCENT_READS_MAPPING_TO_UCSC_GENES: 74.93 PERCENT_READS_MAPPING_TO_UCSC_GENES_PERCENTILE: 5 MAXIMUM_REPLICATE_CORRELATION: 0.62 |
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