Experiment / E4OONIX0DIntegrated lentiMPRA

Pilot K562 lentiMPRA library

Massively parallel characterization of transcriptional regulatory elements

A pilot library of 7,500 designed 200-bp cis-regulatory element and control sequences was assayed in human K562 cells in three independent lentiviral infections. Element activity was quantified from integrated DNA and RNA barcodes as normalized log2(RNA/DNA) scores.

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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.

Organism: Human
Taxonomy ID: NCBITaxon:9606
Biosample: CVCL:0004
Reference genome: GRCh38
Design focus: Region-focused
Region of interest: Not reported / not applicable

Perturbation & assay details

Basal / Untreated

Agilent oligonucleotides were 230 nt, consisting of a fixed 15-nt 5′ adaptor, a 200-bp test element, and a fixed 15-nt 3′ adaptor. A 15-nt random barcode was added during amplification before cloning into the pLS-SceI reporter vector; the lentiviral library was packaged in HEK293T cells, delivered to K562 at an estimated MOI of 10, and harvested after three days. Three independent infections were sequenced for integrated DNA and RNA barcodes with MPRAflow, and activity was reported as median-normalized log2(RNA/DNA).

Processed data

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

Visible columns (42 of 42)

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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 · 42 definitions

element_id: Author-provided identifier for the designed cis-regulatory element or control construct.
element_category: Author-provided category such as potential enhancer, promoter, or control.
orientation: Reporter orientation inferred from the source identifier convention; forward/sense for unsuffixed names and reverse/antisense for reversed names.
chromosome: Primary chromosome coordinate normalized with a chr prefix.
start: Primary GRCh38 element start coordinate from the source design table.
end: Primary GRCh38 element end coordinate from the source design table.
strand: Primary source-design strand.
chr_hg38: Chromosome of the design mapped to GRCh38/hg38, normalized with a chr prefix.
start_hg38: Start coordinate of the design mapped to GRCh38/hg38.
end_hg38: End coordinate of the design mapped to GRCh38/hg38.
strand_hg38: Strand of the GRCh38/hg38 mapping.
chr_hg19: Blank because the pilot K562 design table reports GRCh38 coordinates only.
start_hg19: Blank because the pilot K562 design table reports GRCh38 coordinates only.
end_hg19: Blank because the pilot K562 design table reports GRCh38 coordinates only.
strand_hg19: Blank because the pilot K562 design table reports GRCh38 coordinates only.
sequence_200bp: The 200-bp regulatory sequence tested in the reporter, extracted from the 230-nt oligo by removing the fixed 15-nt flanks.
activity_replicate_1: Published median-normalized log2(RNA/DNA) activity score for biological replicate 1.
activity_replicate_2: Published median-normalized log2(RNA/DNA) activity score for biological replicate 2.
activity_replicate_3: Published median-normalized log2(RNA/DNA) activity score for biological replicate 3.
activity_mean: Published mean activity score across the three biological replicates.
normalized_dna_count_rep1: Published normalized integrated-DNA barcode count for replicate 1.
normalized_dna_count_rep2: Published normalized integrated-DNA barcode count for replicate 2.
normalized_dna_count_rep3: Published normalized integrated-DNA barcode count for replicate 3.
normalized_rna_count_rep1: Published normalized RNA barcode count for replicate 1.
normalized_rna_count_rep2: Published normalized RNA barcode count for replicate 2.
normalized_rna_count_rep3: Published normalized RNA barcode count for replicate 3.
rna_dna_ratio_rep1: Published normalized RNA/DNA ratio for replicate 1.
rna_dna_ratio_rep2: Published normalized RNA/DNA ratio for replicate 2.
rna_dna_ratio_rep3: Published normalized RNA/DNA ratio for replicate 3.
log2_activity_rep1: Full-precision replicate-level log2(RNA/DNA) score from the source replicate sheet for replicate 1.
log2_activity_rep2: Full-precision replicate-level log2(RNA/DNA) score from the source replicate sheet for replicate 2.
log2_activity_rep3: Full-precision replicate-level log2(RNA/DNA) score from the source replicate sheet for replicate 3.
observed_barcodes_rep1: Number of independent element-associated barcodes observed in replicate 1.
observed_barcodes_rep2: Number of independent element-associated barcodes observed in replicate 2.
observed_barcodes_rep3: Number of independent element-associated barcodes observed in replicate 3.
mean_normalized_dna_count: Mean normalized DNA barcode count across the three replicates.
mean_normalized_rna_count: Mean normalized RNA barcode count across the three replicates.
mean_observed_barcodes: Mean observed barcode count across the three replicates.
min_observed_barcodes: Minimum observed barcode count among the three replicates.
total_observed_barcodes: Sum of observed barcode counts across the three replicates.
source_activity_table: Supplementary activity workbook and cell-type sheet used to obtain the activity values.
qc_pass: Boolean package-QC flag; true for every retained row in this table.

Quality control

The authors removed elements measured with fewer than 10 independent barcodes, median-normalized activity within each replicate, and averaged three independent infections. Package QC retained 7,300 rows from the published summary activity records after requiring finite activity values, a matching valid 200-bp design sequence, three replicate-level barcode/count records, and at least 10 observed barcodes in each replicate; non-element or non-finite records were excluded.

Curation notes

The pilot K562 design workbook notes 41 duplicate design names caused by repeated Agilent-array representation; the duplicate rows were identical, so one annotation was retained per activity identifier. The raw_data archive preserves the complete final supplementary-table ZIP, while raw sequencing reads were intentionally omitted. One beta-globin control uses a bracketed coordinate name in the design sheet and was joined after deterministic bracket normalization.

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