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Mapping of H1 Cell Line smRNA-Seq Data
Illumina reads produced by smRNA-Seq on the H1 Cell Line, Library H1EScd1 batch2 vial1 were mapped to the human genome using Pash.


Project News:
2010/11/5:
ANALYSIS XML file 'ucsf-ubc.smrna-seq.level.1-2.xml' uploaded



alias: HS1295-1_42ERCAAXX.hg19.level.1
Analysis Center: EDACC
Analysis File Type: .bed
Analysis File Name: UCSF-UBC.H1.smRNA-Seq.H1EScd1_batch2_vial1.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 2
PERCENT_READS_MAPPING_TO_miRBase_v16_miRNA: 24.4
PERCENT_READS_MAPPING_TO_REPEATMASKER_RNA_REPEATS: 34.9

 

 


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