Experiment / E0KWBYXV7Integrated lentiMPRA

Library Alpha bulk lentiMPRA of CD55-positive HSPCs

Lentiviral single-cell MPRA of synthetic enhancers reveals motif affinity-based encoding of cell state specificity

Bulk validation lentiMPRA was performed on two biological replicates of FACS-sorted CD55-positive primary mouse HSPCs using the Alpha synthetic enhancer library. The table reports replicate RNA/DNA counts, normalized counts, and mean log2 RNA/DNA activity.

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

FACS-sorted CD55-positive HSPC fraction; Basal / Untreated

Lentiviral genomic integration with barcode-based reporter RNA/DNA normalization. Two biological replicates were measured for the CD55-sorted HSPC condition; log2_ratio_mean is the source mean.norm activity score.

Processed data

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

Visible columns (31 of 31)
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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 · 31 definitions
study_id
Parent study identifier.
experiment_id
Child experiment identifier.
condition
FACS-sorted bulk MPRA condition.
source_row_id
1-based row number in the source Figshare RDS object before QC filtering.
element_id
Source bulk construct identifier.
crs_id
Source bulk construct identifier (CRS).
design_name
Enhancer design label joined through bulk_meta_libAlpha.rds.
sequence
DNA sequence joined to the Alpha design from Additional file 4/Table S3.
tf_1
Primary transcription factor motif identity, when annotated.
tf_2
Second transcription factor motif identity, when annotated.
motif_affinity_1
Primary motif affinity/likelihood annotation.
motif_affinity_2
Second motif affinity/likelihood annotation.
motif_count
Number of motif repeats/sites in the design.
orientation_1
Primary motif orientation.
orientation_2
Second motif orientation.
spacer_bp
Spacer length in base pairs.
design_replicate
Design replicate annotation.
control_class
Derived class such as synthetic, positive_control, inert_control, or qc_failure_label.
is_endogenous
Whether the tested element is annotated as endogenous genomic sequence; FALSE for the Alpha synthetic library.
rna_count_rep1
Raw reporter RNA count in bulk replicate 1.
dna_count_rep1
Raw DNA/barcode count in bulk replicate 1.
rna_norm_rep1
Library-size-normalized reporter RNA count in replicate 1.
dna_norm_rep1
Library-size-normalized DNA/barcode count in replicate 1.
log2_ratio_rep1
Source log2 RNA/DNA activity score for replicate 1.
rna_count_rep2
Raw reporter RNA count in bulk replicate 2.
dna_count_rep2
Raw DNA/barcode count in bulk replicate 2.
rna_norm_rep2
Library-size-normalized reporter RNA count in replicate 2.
dna_norm_rep2
Library-size-normalized DNA/barcode count in replicate 2.
log2_ratio_rep2
Source log2 RNA/DNA activity score for replicate 2.
log2_ratio_mean
Mean of the two source replicate log2 RNA/DNA activity scores (`mean.norm`).
qc_pass
TRUE for every retained element; source `pass` QC flag and additional DNA/nonmissing-score checks passed.

Quality control

The source bulk object supplies a pass flag generated by the study's bulk lentiMPRA workflow. I retained only pass == TRUE rows with nonzero DNA counts in both replicates and a nonmissing mean.norm score; zero RNA counts were not removed because they are valid low-activity measurements.

Curation notes

The processed table retains 82 of 83 elements. One element failed the deposited source pass flag. Bulk IDs were joined through bulk_meta_libAlpha.rds and annotated with Alpha design sequences and motif metadata. These bulk data are supplied as the study's validation screen.

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