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Mapping of Spleen mRNA-Seq Data
Illumina reads produced by mRNA-Seq on Spleen, Donor STL001 were mapped to the human genome using Pash.
Project News:
2013/6/12: ANALYSIS XML file 'ucsd.mrna-seq.level.1.xml' uploaded
alias: polyA-RNA-seq_STL001SX_r1a.hg19.level.1.release.9
Analysis Center: EDACC Analysis File Type: .bed Analysis File Name: UCSD.Spleen.mRNA-Seq.STL001.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 9 NUMBER_OF_MAPPED_READS: 53,867,274 PERCENT_READS_MAPPING_TO_UCSC_GENES: 77.8 PERCENT_READS_MAPPING_TO_UCSC_GENES_PERCENTILE: 3 MAXIMUM_REPLICATE_CORRELATION: 0.45 |
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