|
| Status |
Public on Apr 28, 2010 |
| Title |
ChIP-Seq analysis of WCE in human H1 cells; 30H81AAXX090613-1-S |
| Sample type |
SRA |
| |
|
| Source name |
H1 stem cells from Cellular Dynamics; 30H81AAXX090613-1-S
|
| Organism |
Homo sapiens |
| Characteristics |
molecule: genomic DNA
disease: none
biomaterial_provider: Cellular Dynamics
biomaterial_type: Cell Line
line: H1
lineage: undifferentiated
differentiation_stage: stage_zero
differentiation_method: none
passage: 32.0
medium: TESR
sex: Male
batch: 0/0/00
experiment_type: ChIP-Seq Input
extraction_protocol: SDS lysis
extraction_protocol_type_of_sonicator: Bioruptor
extraction_protocol_sonication_cycles: 1
chip_protocol: Input
chip_protocol_chromatin_amount: standard
|
| Extracted molecule |
genomic DNA |
| Extraction protocol |
Library construction protocol: Single read - Illumina
|
| |
|
| Library strategy |
ChIP-Seq |
| Library source |
genomic |
| Library selection |
RANDOM |
| Instrument model |
Illumina Genome Analyzer II |
| |
|
| Description |
sample_term_id: EFO_0003042
assay_term_id: OBI_0000716
nucleic_acid_term_id: SO_0000352
Design description: Human Chromatin IP REMC Sequencing on Illumina
Library name: Solexa-12532
EDACC Genboree Experiment Page:
http://genboree.org/java-bin/project.jsp?projectName=XML%20Submissions%2FBroad%2FEXPERIMENT%2FEDACC.2497
EDACC Genboree Sample Page:
http://genboree.org/java-bin/project.jsp?projectName=XML%20Submissions%2FBroad%2FSAMPLE%2FEDACC.2353
****************
For data usage terms and conditions, please refer to:
http://www.drugabuse.gov/funding/funding-opportunities/nih-common-fund/epigenomics-data-access-policies
****************
BED and WIG files were replaced on April 29, 2014
|
| Data processing |
**********************************************************************
ANALYSIS FILE NAME: GSM537682_BI.H1.Input.Solexa-12532.bed
ANALYSIS CENTER: EDACC
ANALYSIS ALIAS: 30H81AAXX090613-1-S.hg19.level.1
ANALYSIS TITLE: Mapping of H1 Cell Line ChIP-Seq Input Data
ANALYSIS DESCRIPTION: Illumina reads produced by ChIP-Seq Input on the H1 Cell Line, Library Solexa-12532 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.4665
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 2
QUALITY SCORES:
NUMBER_OF_Input_EXPERIMENTS_SCORED: 67
FINDPEAKS_SCORE: 0.0139
FINDPEAKS_PERCENTILE: 66
HOTSPOT_SCORE: 0.0809
HOTSPOT_PERCENTILE: 61
IROC_SCORE: 0.0
IROC_PERCENTILE: NA
POISSON_SCORE: 0.1225
POISSON_PERCENTILE: 1
**********************************************************************
ANALYSIS FILE NAME: GSM537682_BI.H1.Input.Solexa-12532.wig
ANALYSIS CENTER: EDACC
ANALYSIS ALIAS: 30H81AAXX090613-1-S.hg19.level.2
ANALYSIS TITLE: Raw Signal Density Graphs of H1 Cell Line ChIP-Seq Input Data
ANALYSIS DESCRIPTION: Illumina ChIP-Seq Input read mappings from the H1 Cell Line, Library Solexa-12532 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.4939
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 2
BROWSER_TRACK_NAME: H1 Input 32
BROWSER_TRACK_DESCRIPTION: BI H1 Cell Line ChIP-Seq Input Library Solexa-12532 EA Release 2
QUALITY SCORES:
NUMBER_OF_Input_EXPERIMENTS_SCORED: 67
FINDPEAKS_SCORE: 0.0139
FINDPEAKS_PERCENTILE: 66
HOTSPOT_SCORE: 0.0809
HOTSPOT_PERCENTILE: 61
IROC_SCORE: 0.0
IROC_PERCENTILE: NA
POISSON_SCORE: 0.1225
POISSON_PERCENTILE: 1
**********************************************************************
|
| |
|
| Submission date |
Apr 26, 2010 |
| Last update date |
May 15, 2019 |
| Contact name |
BROAD INSTITUTE |
| E-mail(s) |
rharris1@bcm.tmc.edu
|
| Organization name |
Broad Institute
|
| Street address |
-
|
| City |
Cambridge |
| State/province |
MA |
| ZIP/Postal code |
02142 |
| Country |
USA |
| |
|
| Platform ID |
GPL9115 |
| Series (1) |
| GSE17312 |
BI Human Reference Epigenome Mapping Project |
|
| Relations |
| SRA |
SRX019897 |
| BioSample |
SAMN00012247 |
| Named Annotation |
GSM537682_BI.H1.Input.Solexa-12532.wig.gz |
