Experiment / E1LTB5QEWEpisomal Plasmid MPRA

HeLa MPRNA screen for lncRNA nuclear-enrichment sequences

High-throughput identification of RNA nuclear enrichment sequences

A pool of 11,969 153-nt oligos densely tiled 38 lncRNA transcripts (mostly 10-nt spacing; 40-nt spacing for kcnq1ot1) was cloned 3' of noncoding fsSox2 and transiently transfected into HeLa. Six biological replicates were fractionated into nuclei and matched total-RNA samples, and barcode RNA-seq quantified nuclear enrichment.

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

Transiently transfected minCMV-fsSox2 reporter plasmid library; each 110-nt lncRNA tile was appended 3' of fsSox2 and paired with a unique 10-nt barcode. After 48 h in HeLa cells, nuclear and matched total-RNA fractions were sequenced by targeted barcode RNA-seq; library-size-normalized oligo counts and modeled nuclear-enrichment differential regions were reported.

Processed data

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

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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 · 37 definitions
element_id
Original unique oligo identifier from GEO, composed of transcript accession, 0-based oligo index, and 10-nt barcode.
transcript_name
Human-readable lncRNA/library name from the oligo-pool metadata.
transcript_accession
Transcript accession or construct identifier used to match the GEO normalized-count row to the library metadata.
oligo_index_0based
0-based tile index within the transcript/library member.
barcode_10nt
Unique 10-nucleotide oligo barcode used for targeted sequencing assignment.
tile_start_1based
1-based inclusive start of the variable RNA tile within the transcript sequence, derived from the library step size.
tile_end_1based
1-based inclusive end of the variable RNA tile within the transcript sequence, derived from oligoGames library metadata.
tile_length
Length in nucleotides of the variable RNA tile.
fish_class
smFISH localization class recorded for the parental lncRNA in the pool metadata; * denotes unspecified.
window_step_nt
Spacing in nucleotides between successive tiled oligos.
nuclei_rep1_norm_count
GEO library-size-normalized oligo count for nuclear biological replicate 1.
nuclei_rep2_norm_count
GEO library-size-normalized oligo count for nuclear biological replicate 2.
nuclei_rep3_norm_count
GEO library-size-normalized oligo count for nuclear biological replicate 3.
nuclei_rep4_norm_count
GEO library-size-normalized oligo count for nuclear biological replicate 4.
nuclei_rep5_norm_count
GEO library-size-normalized oligo count for nuclear biological replicate 5.
nuclei_rep6_norm_count
GEO library-size-normalized oligo count for nuclear biological replicate 6.
total_rep1_norm_count
GEO library-size-normalized oligo count for matched total-RNA biological replicate 1.
total_rep2_norm_count
GEO library-size-normalized oligo count for matched total-RNA biological replicate 2.
total_rep3_norm_count
GEO library-size-normalized oligo count for matched total-RNA biological replicate 3.
total_rep4_norm_count
GEO library-size-normalized oligo count for matched total-RNA biological replicate 4.
total_rep5_norm_count
GEO library-size-normalized oligo count for matched total-RNA biological replicate 5.
total_rep6_norm_count
GEO library-size-normalized oligo count for matched total-RNA biological replicate 6.
nuclei_mean_norm_count
Arithmetic mean of the six nuclear normalized counts.
nuclei_median_norm_count
Median of the six nuclear normalized counts.
total_mean_norm_count
Arithmetic mean of the six matched total-RNA normalized counts.
total_median_norm_count
Median of the six matched total-RNA normalized counts.
median_nuclei_minus_total
Median across paired replicates of nuclear normalized count minus total-RNA normalized count; positive values indicate greater nuclear signal.
log2_nuclei_total_ratio_pseudocount_1
Log2 of (median nuclear normalized count + 1) divided by (median total-RNA normalized count + 1).
nuclei_detected_reps
Number of the six nuclear replicates with normalized count greater than zero; used for row-level QC.
total_detected_reps
Number of the six total-RNA replicates with normalized count greater than zero; used for row-level QC.
qc_pass
TRUE for rows retained after requiring at least 3 detected nuclear and 3 detected total-RNA replicates.
published_dr_overlap
TRUE when the derived transcript-local tile interval overlaps one or more of the 109 published differential regions.
dr_ids
Local identifiers (DR001-DR109) for overlapping published differential regions, in the order supplied by GEO.
dr_qvalue_min
Smallest published Benjamini-Hochberg q-value among overlapping differential regions.
dr_pvalue_min
Smallest published empirical p-value among overlapping differential regions.
dr_statistic_max
Largest published differential-region summary statistic among overlapping regions.
dr_coordinates
Semicolon-separated published differential-region identifiers and transcript-local inclusive coordinates in the form DR###:start-end.

Quality control

The authors required recovery of more than 70% of the oligo pool in each sequencing sample, used an exact 10-nt barcode match with a stringent upstream sequence mismatch filter, and analyzed six biological replicates. For this package, an oligo was retained only when its GEO normalized count was greater than zero in at least 3 of 6 nuclear replicates and at least 3 of 6 total-RNA replicates; 11,132 of 11,969 input oligos (93.01%) passed. The table retains all six replicate values, including zeros, for the retained oligos.

Curation notes

This is the paper's single MPRNA screen, not an allele-contrast enhancer MPRA: the library densely tiles transcript regions and measures RNA nuclear retention. The six Nuclei and six Total columns are the authors' processed biological-replicate labels; GEO sample records also document technical replicate sequencing. Tile coordinates are transcript-local 1-based coordinates derived from oligoMeta.tsv using the authors' oligoGames convention, including the final-oligo endpoint correction. DR annotations use the published chr/start/end intervals and q-values from GSE98828_oligoGames.DRs.tsv.gz; the raw indexStart/indexEnd fields are retained in the source file but were not used for overlap because they are on the authors' modeled index scale. The experiment is performed in human HeLa cells (Cellosaurus CVCL:0030); the pool additionally contains a mouse FIRRE library member (FIRRE(MM)). The processed table contains barcode and tile identity but no oligo sequence string because the authors' GEO normalized-count release does not provide the variable sequences.

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