|
| Status |
Public on Sep 21, 2010 |
| Title |
Chromatin accessibility assay of Fetal brain tissue; DS11877 |
| Sample type |
SRA |
| |
|
| Source name |
Fetal Brain primary tissue, day 122; DS11877
|
| Organism |
Homo sapiens |
| Characteristics |
molecule: genomic DNA
disease: None
biomaterial_provider: University of Washington, Congenital Defects Lab. Ian Glass
biomaterial_type: Primary Tissue
tissue_type: fetal brain
tissue_depot: UW
collection_method: fetal
donor_id: H-22510
donor_age: 122 days
donor_health_status: NA
donor_sex: Male
donor_ethnicity: NA
experiment_type: Chromatin Accessibility
extraction_protocol: Qiagen minElut
dnase_protocol: Stamlab DNase Protocol
|
| Extracted molecule |
genomic DNA |
| Extraction protocol |
Library construction protocol: Single read - Illumina
|
| |
|
| Library strategy |
DNase-Hypersensitivity |
| Library source |
genomic |
| Library selection |
DNAse |
| Instrument model |
Illumina Genome Analyzer II |
| |
|
| Description |
sample_term_id: UBERON_0000955
assay_term_id: OBI_0001853
nucleic_acid_term_id: SO_0000352
Design description: Chromatin accessibility determination via DNase-seq
Library name: DS11877
EDACC Genboree Experiment Page:
http://genboree.org/java-bin/project.jsp?projectName=XML%20Submissions%2FUniversity%20of%20Washington%2FEXPERIMENT%2FEDACC.3110
EDACC Genboree Sample Page:
http://genboree.org/java-bin/project.jsp?projectName=XML%20Submissions%2FUniversity%20of%20Washington%2FSAMPLE%2FEDACC.2448
****************
For data usage terms and conditions, please refer to:
http://www.drugabuse.gov/funding/funding-opportunities/nih-common-fund/epigenomics-data-access-policies
****************
|
| Data processing |
**********************************************************************
ANALYSIS FILE NAME: GSM595913_fBrain-DS11877.hg19.bam
ANALYSIS ALIAS: DS11877-align
ANALYSIS TITLE: Alignments DS11877
ANALYSIS DESCRIPTION: Bowtie (v0.12.5) alignments of Chromatin Accessibility Illumina sequencing lane data to the human genome The Genome Reference Consortium GRCh37 (hg19)
ANALYSIS TYPE: REFERENCE_ALIGNMENT
EDACC Genboree Analysis Page:
DATA_ANALYSIS_LEVEL: 1
EXPERIMENT_TYPE: Chromatin Accessibility
SOFTWARE: Bowtie
SOFTWARE_VERSION: 0.12.5
MAXIMUM_ALIGNMENT_LENGTH: 36
MISMATCHES_ALLOWED: 2
ALIGNMENTS_ALLOWED: 1
TREATMENT_OF_MULTIPLE_ALIGNMENTS: not submitted
TREATMENT_OF_IDENTICAL_ALIGNMENTS_OF_MULTIPLE_READS: allowed
ALIGNMENT_POSTPROCESSING: none
**********************************************************************
ANALYSIS FILE NAME: GSM595913_fBrain-DS11877.75.20.filtered-density.36.hg19.wig
ANALYSIS ALIAS: DS11877-signal
ANALYSIS TITLE: Signal DS11877
ANALYSIS DESCRIPTION: Chromatin Accessibility data with a sliding window (+/-75bp) summation at 20 bp steps across the genome
ANALYSIS TYPE: ABUNDANCE_MEASUREMENT
EDACC Genboree Analysis Page:
DATA_ANALYSIS_LEVEL: 2
EXPERIMENT_TYPE: Chromatin Accessibility
SOFTWARE: signalmap
SOFTWARE_VERSION: 1.0
READ_EXTENSION: 150
GENOMIC_WINDOW: 20bp
TREATMENT_OF_REGIONS_PRONE_TO_MULTIPLE_ALIGNMENTS: NA
**********************************************************************
ANALYSIS FILE NAME: GSM595913_UW.Fetal_Brain.ChromatinAccessibility.H-22510.DS11877.bed
ANALYSIS ALIAS: DS11877.hg19.level.1
ANALYSIS TITLE: Mapping of Fetal Brain Chromatin Accessibility Data
ANALYSIS DESCRIPTION: Illumina reads produced by DNAse-Seq on Fetal Brain, Donor H-22510, Library DS11877 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.4124
DATA_ANALYSIS_LEVEL: 1
EXPERIMENT_TYPE: Chromatin Accessibility
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 2
QUALITY SCORES:
NUMBER_OF_CHROMATIN_ACCESSIBILITY_EXPERIMENTS_SCORED: 40
FINDPEAKS_SCORE: 0.6764
FINDPEAKS_PERCENTILE: 82
HOTSPOT_SCORE: 0.559
HOTSPOT_PERCENTILE: 85
IROC_SCORE: 0.9975
IROC_PERCENTILE: 60
POISSON_SCORE: 0.5602
POISSON_PERCENTILE: 65
**********************************************************************
ANALYSIS FILE NAME: GSM595913_UW.Fetal_Brain.ChromatinAccessibility.H-22510.DS11877.wig
ANALYSIS ALIAS: DS11877.hg19.level.2
ANALYSIS TITLE: Raw Signal Density Graphs of Fetal Brain Chromatin Accessibility Data
ANALYSIS DESCRIPTION: Illumina DNAse-Seq read mappings from Fetal Brain, Donor H-22510, Library DS11877 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.4084
DATA_ANALYSIS_LEVEL: 2
EXPERIMENT_TYPE: Chromatin Accessibility
GENOME_ASSEMBLY: NCBI Build GRCh37/UCSC Build hg19
SOFTWARE: In house programs and scripts
SOFTWARE_VERSION: NA
READ_EXTENSION: 0bp
GENOMIC_WINDOW: 150bp
TREATMENT_OF_REGIONS_PRONE_TO_MULTIPLE_ALIGNMENTS: None
RELEASE_NUMBER: Human Epigenome Atlas 2
BROWSER_TRACK_NAME: FB DNase 10 77
BROWSER_TRACK_DESCRIPTION: UW Fetal Brain DNase Hypersensitivity Donor H-22510 Library DS11877 EA Release 2
QUALITY SCORES:
NUMBER_OF_CHROMATIN_ACCESSIBILITY_EXPERIMENTS_SCORED: 40
FINDPEAKS_SCORE: 0.6764
FINDPEAKS_PERCENTILE: 82
HOTSPOT_SCORE: 0.559
HOTSPOT_PERCENTILE: 85
IROC_SCORE: 0.9975
IROC_PERCENTILE: 60
POISSON_SCORE: 0.5602
POISSON_PERCENTILE: 65
|
| |
|
| Submission date |
Sep 20, 2010 |
| Last update date |
May 15, 2019 |
| Contact name |
Northwest REMC |
| E-mail(s) |
[email protected]
|
| Organization name |
University of Washington
|
| Street address |
-
|
| City |
Seattle |
| State/province |
WA |
| ZIP/Postal code |
98195 |
| Country |
USA |
| |
|
| Platform ID |
GPL9115 |
| Series (1) |
| GSE18927 |
University of Washington Human Reference Epigenome Mapping Project |
|
| Relations |
| SRA |
SRX027076 |
| BioSample |
SAMN00113444 |
| Named Annotation |
GSM595913_UW.Fetal_Brain.ChromatinAccessibility.H-22510.DS11877.wig.gz |
| Named Annotation |
GSM595913_fBrain-DS11877.75.20.filtered-density.36.hg19.wig.gz |
