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Status |
Public on Mar 23, 2011 |
Title |
Reference Epigenome: ChIP-Seq Input from hESC H9 Cells; renlab.Input.hESC.H9.01.01 |
Sample type |
SRA |
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|
Source name |
Human embryonic stem cells received from the James Thompson laboratory. Cells are from the H9 line.; renlab.Input.hESC.H9.01.01
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Organism |
Homo sapiens |
Characteristics |
sample alias: H9-02 sample common name: H9 Cell Line molecule: genomic DNA disease: None biomaterial_provider: James Thompson Laboratory biomaterial_type: Cell Line line: H9 lineage: Embryonic Stem Cell differentiation_stage: None differentiation_method: None passage: Between 30 and 50 medium: mTeSER Sex: Female batch: H9 experiment_type: ChIP-Seq Input extraction_protocol: See http://bioinformatics-renlab.ucsd.edu/RenLabChipProtocolV1.pdf extraction_protocol_type_of_sonicator: Biorupter extraction_protocol_sonication_cycles: 80 chip_protocol: Input chip_protocol_chromatin_amount: 500 micrograms
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Extracted molecule |
genomic DNA |
Extraction protocol |
Library construction protocol: See http://bioinformatics-renlab.ucsd.edu/RenLabLibraryProtocolV1.pdf
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Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
RANDOM |
Instrument model |
Illumina HiSeq 2000 |
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Description |
sample_term_id: NTR_0000838 assay_term_id: OBI_0000716 nucleic_acid_term_id: SO_0000352 Design description: ChIP-Seq Input from hESC H9 Cells. Sequencing was done on the Illumina HiSeq 2000 platform. Library name: SKH9-4 EDACC Genboree Experiment Page: http://genboree.org/java-bin/project.jsp?projectName=XML%20Submissions%2FUCSD%2FEXPERIMENT%2FEDACC.5993 EDACC Genboree Sample Page: http://genboree.org/java-bin/project.jsp?projectName=XML%20Submissions%2FUCSD%2FSAMPLE%2FEDACC.4286 **************** For data usage terms and conditions, please refer to: http://www.drugabuse.gov/funding/funding-opportunities/nih-common-fund/epigenomics-data-access-policies ****************
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Data processing |
**********************************************************************
ANALYSIS FILE NAME: GSM667643_UCSD.H9.Input.SKH9-4.bed ANALYSIS CENTER: EDACC ANALYSIS ALIAS: renlab.Input.hESC.H9.01.01.hg19.level.1.release.3 ANALYSIS TITLE: Mapping of H9 Cell Line ChIP-Seq Input Data ANALYSIS DESCRIPTION: Illumina reads produced by ChIP-Seq Input on the H9 Cell Line, Library SKH9-4 were mapped to the human genome using Pash. ANALYSIS TYPE: REFERENCE_ALIGNMENT EDACC Genboree Analysis Page: http://genboree.org/java-bin/project.jsp?projectName=XML%20Submissions%2FEDACC%2FANALYSIS%2FEDACC.6286 DATA_ANALYSIS_LEVEL: 1 EXPERIMENT_TYPE: ChIP-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: If multiple reads map to the same start position on the + strand or stop position on the - strand, only a single read is retained. ALIGNMENT_POSTPROCESSING: None READ_EXTENSION: 200bp RELEASE_NUMBER: Human Epigenome Atlas 3
QUALITY SCORES: NUMBER_OF_Input_EXPERIMENTS_SCORED_IN_THIS_RELEASE: 30 FINDPEAKS_SCORE: 0.0124 FINDPEAKS_PERCENTILE: 93 HOTSPOT_SCORE: 0.0778 HOTSPOT_PERCENTILE: 90 IROC_SCORE: 0.9959 IROC_PERCENTILE: 59 POISSON_SCORE: 0.0966 POISSON_PERCENTILE: 87
**********************************************************************
ANALYSIS FILE NAME: GSM667643_UCSD.H9.Input.SKH9-4.wig ANALYSIS CENTER: EDACC ANALYSIS ALIAS: renlab.Input.hESC.H9.01.01.hg19.level.2.release.3 ANALYSIS TITLE: Raw Signal Density Graphs of H9 Cell Line ChIP-Seq Input Data ANALYSIS DESCRIPTION: Illumina ChIP-Seq Input read mappings from the H9 Cell Line, Library SKH9-4 were processed into density graphs of raw signal representing the aligned read density. ANALYSIS TYPE: ABUNDANCE_MEASUREMENT EDACC Genboree Analysis Page: http://genboree.org/java-bin/project.jsp?projectName=XML%20Submissions%2FEDACC%2FANALYSIS%2FEDACC.6628 DATA_ANALYSIS_LEVEL: 2 EXPERIMENT_TYPE: ChIP-Seq GENOME_ASSEMBLY: NCBI Build GRCh37/UCSC Build hg19 SOFTWARE: In house programs and scripts SOFTWARE_VERSION: NA READ_EXTENSION: 200bp TREATMENT_OF_IDENTICAL_ALIGNMENTS_OF_MULTIPLE_READS: If multiple reads map to the same start position on the + strand or stop position on the - strand, only a single read is retained. GENOMIC_WINDOW: 20bp TREATMENT_OF_REGIONS_PRONE_TO_MULTIPLE_ALIGNMENTS: None RELEASE_NUMBER: Human Epigenome Atlas 3 BROWSER_TRACK_NAME: H9 Input 4 BROWSER_TRACK_DESCRIPTION: UCSD H9 Cell Line ChIP-Seq Input Library SKH9-4 EA Release 3
QUALITY SCORES: NUMBER_OF_Input_EXPERIMENTS_SCORED_IN_THIS_RELEASE: 30 FINDPEAKS_SCORE: 0.0124 FINDPEAKS_PERCENTILE: 93 HOTSPOT_SCORE: 0.0778 HOTSPOT_PERCENTILE: 90 IROC_SCORE: 0.9959 IROC_PERCENTILE: 59 POISSON_SCORE: 0.0966 POISSON_PERCENTILE: 87
**********************************************************************
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Submission date |
Feb 03, 2011 |
Last update date |
May 15, 2019 |
Contact name |
UCSD AND SALK |
Organization name |
University of California, San Diego
|
Street address |
Health Sciences Drive
|
City |
La Jolla |
State/province |
CA |
ZIP/Postal code |
92092 |
Country |
USA |
|
|
Platform ID |
GPL11154 |
Series (1) |
GSE16256 |
UCSD Human Reference Epigenome Mapping Project |
|
Relations |
SRA |
SRX056745 |
BioSample |
SAMN00117209 |
Named Annotation |
GSM667643_UCSD.H9.Input.SKH9-4.wig.gz |