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| Status |
Public on Dec 10, 2014 |
| Title |
dCP_S2_STARRseq_input |
| Sample type |
SRA |
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| Source name |
whole genome library (in STARR-seq vector)
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| Organism |
Drosophila melanogaster |
| Characteristics |
genotype: y; cn bw sp - sequenced strain (Adams et al. 2000)
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| Extracted molecule |
genomic DNA |
| Extraction protocol |
Genomic DNA (source: embryos of the sequenced strain: y; cn bw sp) was isolated, sheared and size selected (~500bp). Following the instructions of NEBNext® DNA Library Prep Reagent Set for Illumina® (NEB; cat. no. E6000L), Illumina Multiplexing Adapters (Illumina Inc; cat. no. PE-400-1001) were ligated and homology arms for In-Fusion® recombination were added by PCR, followed by recombination into the STARR-seq vector. To construct the dCP STARR-seq vector, the sequence between BglII and FseI from the pGL3-Promoter backbone (Promega; cat. no. E1751) was replaced with the Drosophila Synthetic Core Promoter (DSCP), an ORF (sgGFP, Qbiogene, Inc), a ccdB suicide gene flanked by homology arms (used for cloning the genomic enhancer candidates during library generation), and the pGL3’s SV40 late polyA-signal. The hkCP STARR-seq vector is identical to the dCP STARR-seq vector except we replaced the DSCP with the RpS12 core promoter. The In-Fusion® reactions were transformed (MegaX DH10B; Invitrogen), grown in liquid culture and plasmids were isolated.
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| Library strategy |
OTHER |
| Library source |
genomic |
| Library selection |
other |
| Instrument model |
Illumina Genome Analyzer IIx |
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| Description |
plasmid DNA (containing genomic DNA fragments)
library strategy: STARR-Seq
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| Data processing |
Basecall where performed using Real-Time Analysis (RTA) version > 1.12.4.2 or CASAVA 1.9.1
STARR-Seq:
Reads were mapped to the dm3 genome using bowtie (bowtie -p 4 -f -X 2000 -v 3 -m 1 --best --strata --quiet INDEX -1 reads_1.fa -2 reads_2.fa) excluding chrU, chrUextra, and chrM. We additionally employed redundancy filter to remove clustered reads that could be due to sequence artefacts. For all subsequently analysis we used only reads collapsed on chromosome, start, end, strand (fragments), and merged these fragments from the two replicates. Significantly enriched regions (peaks) were called with an in-house pipeline using read density profiles of STARR-seq and input. We performed hypergeometric tests to assign a p-value to each peak. Enrichment values were corrected within a 95% confidence interval taking into account the number of independent fragments at a single peak summit position.
Processed data files represent data from both replicates.
Genome_build: dm3
Supplementary_files_format_and_content: All processed data files are in plain text. For STARR-seq we report for each peak the chromosome, the summit position, the enrichment over input at the summit, and the p-value.
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| Submission date |
May 23, 2014 |
| Last update date |
May 15, 2019 |
| Contact name |
Alexander Stark |
| Organization name |
Research Institute for Molecular Pathology (IMP), Vienna Biocenter VBC
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| Street address |
Dr Bohr-Gasse 7
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| City |
Vienna |
| ZIP/Postal code |
1030 |
| Country |
Austria |
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| Platform ID |
GPL11203 |
| Series (1) |
| GSE57876 |
Enhancer-core promoter specificity separates developmental and housekeeping regulation |
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| Relations |
| Reanalysis of |
GSM1000404 |
| BioSample |
SAMN02798550 |
| SRA |
SRX551605 |
| Supplementary data files not provided |
SRA Run Selector |
| Raw data are available in SRA |
| Processed data are available on Series record |
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