|
||||||||
Mapping of Fetal Brain smRNA-Seq Data
Illumina reads produced by smRNA-Seq on Fetal Brain, Donor HuFNSC01 were mapped to the human genome using Pash.
Project News:
2011/8/30: ANALYSIS XML file 'ucsf-ubc.smrna-seq.level.1.xml' uploaded
alias: M01581-1.hg19.level.1.release4
Analysis Center: EDACC Analysis File Type: .bed Analysis File Name: UCSF-UBC.Fetal_Brain.smRNA-Seq.HuFNSC01.bed DATA_ANALYSIS_LEVEL: 1 EXPERIMENT_TYPE: smRNA-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: 100 TREATMENT_OF_MULTIPLE_ALIGNMENTS: If a read maps to more than 100 positions it is removed from consideration. TREATMENT_OF_IDENTICAL_ALIGNMENTS_OF_MULTIPLE_READS: None ALIGNMENT_POSTPROCESSING: None RELEASE_NUMBER: Human Epigenome Atlas 4 NUMBER_OF_MAPPED_READS: 7,156,714 PERCENT_READS_MAPPING_TO_miRBase_v16_miRNA: 89.53 PERCENT_READS_MAPPING_TO_miRBase_v16_miRNA_PERCENTILE: 80 MAXIMUM_REPLICATE_CORRELATION: 0.996 |
||||||||
|
|
||||||||
|
||||||||