Experiment / E8HIE2F2VTargeted Genomic Integration MPRA

Full-length Oak/ChII promoter CRE-seq validation

Cis-regulatory variants affect gene expression dynamics in yeast

Full-length promoters from ALD5, GND2, and PHO3 in Oak and ChII backgrounds were barcoded and integrated at URA3 in the Oak × ChII diploid. The supplied full-length count/activity file was summarized by gene, allele, and measured timepoint.

Processed tables are specific to each experiment. Column names, units, measurements, and table structure are not standardized across the database. Check this experiment’s column definitions and quality-control notes before comparing or combining data.

Perturbation & assay details

Diauxic-shift time course in YPD at 30°C; no exogenous treatment

Full-length promoter CRE-seq extension using the pIM202/YFP/barcode reporter integrated at the URA3 locus. Oak and ChII full-length promoter constructs were assayed by barcode RNA/DNA ratios; the supplied file contains the source exp value, RNA count, and DNA count but does not retain barcode sequence identifiers.

Processed data

50 rows per page. Click a cell to inspect its full value.

Visible columns (19 of 19)
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Filters apply to this table only. The CSV download contains the complete processed table; filtered rows are available through the API.

Column dictionary · 19 definitions
element_id
Unique full-length promoter construct identifier.
gene_name
Common gene name: ALD5, GND2, or PHO3.
systematic_gene_id
Systematic S. cerevisiae gene identifier corresponding to gene_name.
allele
Promoter allele, Oak or ChII.
allele_label
Human-readable promoter allele label.
construct_type
Full-length promoter reporter construct.
promoter_scope
Promoter scope represented by the construct; full_length.
n_barcodes_total
Number of barcodes designed per full-length promoter construct.
n_observations
Number of source records observed in this gene-allele-timepoint cell.
qc_pass_rate
n_observations divided by four designed barcode observations; source records lack barcode IDs.
timepoint
Sequential measured timepoint label assigned after sorting the source time values.
time_hours
Measured sampling time in hours from the source file.
mean_rna_count
Mean supplied RNA barcode count for this gene, allele, and timepoint.
mean_dna_count
Mean supplied DNA barcode count for this gene, allele, and timepoint.
mean_log2_activity
Mean supplied exp value, representing the source barcode RNA/DNA activity on a log2 scale.
sem_log2_activity
Standard error of the supplied exp values within this gene-allele-timepoint cell.
mean_activity_over_time
Mean of the timepoint mean_log2_activity values for this promoter allele.
sd_activity_over_time
Standard deviation of timepoint mean_log2_activity values for this promoter allele.
n_timepoints_with_activity
Number of measured timepoints contributing to the promoter-allele activity summary.

Quality control

The supplied full.length.counts.csv contains 360 positive RNA/DNA observations for six promoter-allele constructs across 20 measured timepoints; no zero-count records were present and no additional author filter was documented for this validation file. All positive observations were retained and aggregated by gene, allele, and timepoint. Four barcodes were designed per construct, but the source file does not identify individual barcode sequences and contains 2–4 observed records per gene-allele-timepoint cell.

Curation notes

The full-length promoter records are a validation extension of the short CRE-seq assay, not a separate genomic region screen. The source table contains no barcode sequence or construct sequence columns, so sequence-level details remain in the short-library raw files and the full-length table is intentionally an aggregate summary.

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