Experiment / E5LA4OI3PEpisomal Plasmid MPRA

7.5k positive- and negative-control allelic MPRA library across LCLs

Direct identification of hundreds of expression-modulating variants using a multiplexed reporter assay

A follow-up 7,500-oligo episomal MPRA library tested 264 positive-control variants from the 79k screen together with location-matched and genome-wide negative controls in NA12878 and NA19239 lymphoblastoid cell lines. The table pairs the deposited allele-A and allele-B rows and reports count-derived RNA-over-DNA activity and allelic differences.

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

Basal / Untreated

The smaller follow-up library used the same synthetic oligo/minimal-promoter/GFP reporter architecture and 20-nucleotide 3' UTR barcode strategy as the 79k library. The deposited 7.5k count matrix contains five plasmid-input replicates, five NA12878 RNA replicates, and three NA19239 RNA replicates. The authors additionally downsampled the 7.5k barcode data in their cross-library sensitivity analysis; this package uses the deposited collapsed-count matrix as supplied and does not perform a second barcode-level downsampling.

Processed data

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

Visible columns (30 of 30)
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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 · 30 definitions
element_id
Pair identifier formed from the deposited count IDs after removing the central allele-A/B marker; source suffixes such as _RC and _alt-1 are retained.
variant_id
Coordinate-style or rsID identifier for the centered variant, with source _RC and _alt-1 suffixes removed.
variant_type
SNP for rsID records; indel_or_coordinate_id for coordinate-style insertion/deletion records.
orientation
Inferred from the source pair ID: reverse when the pair carries the _RC suffix, otherwise forward.
neighboring_haplotype
Inferred source suffix: alt-1 when the pair carries _alt-1, otherwise ref/primary construct; this is not a claim about the centered A/B allele sequence.
allele_a_oligo_id
Exact deposited GEO collapsed-count row ID containing the central allele-A marker.
allele_b_oligo_id
Exact deposited GEO collapsed-count row ID containing the central allele-B marker.
qc_status
Package-level status; only pairs passing the paired plasmid-input threshold are emitted.
qc_min_dna_count
Smaller of allele-A and allele-B summed plasmid-input counts across the five deposited plasmid replicates.
allele_a_dna_count_sum
Sum of the five unnormalized deposited plasmid-input counts for allele A.
allele_b_dna_count_sum
Sum of the five unnormalized deposited plasmid-input counts for allele B.
allele_a_dna_cpm_mean
Mean allele-A plasmid-input count per million across the five plasmid replicates, using each sample's total oligo count for normalization.
allele_b_dna_cpm_mean
Mean allele-B plasmid-input count per million across the five plasmid replicates, using each sample's total oligo count for normalization.
allele_a_na12878_rna_count_sum
Sum of allele-A counts across the five deposited NA12878 RNA replicates.
allele_b_na12878_rna_count_sum
Sum of allele-B counts across the five deposited NA12878 RNA replicates.
allele_a_na12878_rna_cpm_mean
Mean allele-A NA12878 RNA count per million across the five RNA replicates.
allele_b_na12878_rna_cpm_mean
Mean allele-B NA12878 RNA count per million across the five RNA replicates.
allele_a_na12878_log2_activity
Derived NA12878 allele-A activity: log2((RNA CPM mean + 1)/(DNA CPM mean + 1)).
allele_b_na12878_log2_activity
Derived NA12878 allele-B activity: log2((RNA CPM mean + 1)/(DNA CPM mean + 1)).
na12878_allelic_log2_effect_b_minus_a
Derived NA12878 allele-B-minus-allele-A activity difference on the log2 scale.
allele_a_na19239_rna_count_sum
Sum of allele-A counts across the three deposited NA19239 RNA replicates.
allele_b_na19239_rna_count_sum
Sum of allele-B counts across the three deposited NA19239 RNA replicates.
allele_a_na19239_rna_cpm_mean
Mean allele-A NA19239 RNA count per million across the three RNA replicates.
allele_b_na19239_rna_cpm_mean
Mean allele-B NA19239 RNA count per million across the three RNA replicates.
allele_a_na19239_log2_activity
Derived NA19239 allele-A activity: log2((RNA CPM mean + 1)/(DNA CPM mean + 1)).
allele_b_na19239_log2_activity
Derived NA19239 allele-B activity: log2((RNA CPM mean + 1)/(DNA CPM mean + 1)).
na19239_allelic_log2_effect_b_minus_a
Derived NA19239 allele-B-minus-allele-A activity difference on the log2 scale.
allele_a_combined_lcl_log2_activity
Derived combined-LCL allele-A activity, weighted by the deposited replicate counts: five NA12878 replicates and three NA19239 replicates.
allele_b_combined_lcl_log2_activity
Derived combined-LCL allele-B activity, weighted by the deposited replicate counts: five NA12878 replicates and three NA19239 replicates.
combined_lcl_allelic_log2_effect_b_minus_a
Derived combined-LCL allele-B-minus-allele-A activity difference on the log2 scale.

Quality control

The authors' barcode reconstruction and read filtering are described in the supplemental experimental procedures; the original follow-up analysis matched the 79k library's expression and allelic-skew calling framework and used downsampling for a specific cross-library comparison. For this package, the 7,500 deposited oligo rows were paired by the embedded central allele marker A or B, yielding 3,750 complete allele pairs. Both alleles were required to have at least 20 summed plasmid-input reads across Plasmid_r1 through Plasmid_r5; 3,704 pairs passed and 46 low-input pairs were excluded. Count-derived activity values are per-sample CPM summaries with a 1-count-on-the-CPM-scale pseudocount. Because this release does not contain the 7.5k author summary statistics workbook, no new significance calls are asserted here.

Curation notes

The raw 7.5k count identifiers encode the central allele as A or B and may carry _RC and _alt-1 source suffixes for orientation/alternate construct variants. The table deliberately labels the contrast A/B rather than asserting reference/alternative nucleotide identity because the 7.5k collapsed-count release does not include a separate allele-annotation table. The authors' 7.5k analysis downsampled barcodes for cross-library comparison; this element-level package retains the deposited count values and reports no re-fit p-values.

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