type: position_score table: filename: ENCFF131VCS.tabix.bed.gz header_mode: none zero_based: true format: tabix chrom: column_index: 0 pos_begin: column_index: 1 pos_end: column_index: 2 scores: - id: TF_ChIP-seq_ENCSR932BNN column_index: 3 type: float desc: signal histogram: type: number number_of_bins: 100 meta: summary: 'ChIP-seq ENCSR932BNN [TISSUE: Homo sapiens HepG2 genetically modified (insertion) using CRISPR targeting H. sapiens ARID3A, TARGET: ARID3A]' description: '**status**: released **biological\_replicates**: Rep 1, Rep 2 **summary**: genetically modified (insertion) using CRISPR targeting H. sapiens ARID3A **output\_type**: IDR thresholded peaks **audit\_internal\_action**: Released analysis {ENCAN564SFI|/analyses/ENCAN564SFI/} has in progress subobject quality standard {encode4-tf-chip|/quality-standards/encode4-tf-chip/} **audit\_warning**: NRF (Non Redundant Fraction) is equal to the result of the division of the number of reads after duplicates removal by the total number of reads. An NRF value in the range 0 - 0.5 is poor complexity, 0.5 - 0.8 is moderate complexity, and > 0.8 high complexity. NRF value > 0.8 is recommended, but > 0.5 is acceptable. ENCODE processed alignments file {ENCFF817AFA|/files/ENCFF817AFA/} processed by ChIP-seq ENCODE4 v1.8.0 GRCh38 pipeline was generated from a library with NRF value of 0.80. **audit\_warning**: PBC1 (PCR Bottlenecking Coefficient 1, M1/M\_distinct) is the ratio of the number of genomic locations where exactly one read maps uniquely (M1) to the number of genomic locations where some reads map (M\_distinct). A PBC1 value in the range 0 - 0.5 is severe bottlenecking, 0.5 - 0.8 is moderate bottlenecking, 0.8 - 0.9 is mild bottlenecking, and > 0.9 is no bottlenecking. PBC1 value > 0.9 is recommended, but > 0.8 is acceptable. ENCODE processed alignments file {ENCFF817AFA|/files/ENCFF817AFA/} processed by ChIP-seq ENCODE4 v1.8.0 GRCh38 pipeline was generated from a library with PBC1 value of 0.80. **audit\_warning**: PBC2 (PCR Bottlenecking Coefficient 2, M1/M2) is the ratio of the number of genomic locations where exactly one read maps uniquely (M1) to the number of genomic locations where two reads map uniquely (M2). A PBC2 value in the range 0 - 1 is severe bottlenecking, 1 - 3 is moderate bottlenecking, 3 - 10 is mild bottlenecking, > 10 is no bottlenecking. PBC2 value > 10 is recommended, but > 3 is acceptable. ENCODE processed alignments file {ENCFF817AFA|/files/ENCFF817AFA/} processed by ChIP-seq ENCODE4 v1.8.0 GRCh38 pipeline was generated from a library with PBC2 value of 5.05. **audit\_warning**: PBC1 (PCR Bottlenecking Coefficient 1, M1/M\_distinct) is the ratio of the number of genomic locations where exactly one read maps uniquely (M1) to the number of genomic locations where some reads map (M\_distinct). A PBC1 value in the range 0 - 0.5 is severe bottlenecking, 0.5 - 0.8 is moderate bottlenecking, 0.8 - 0.9 is mild bottlenecking, and > 0.9 is no bottlenecking. PBC1 value > 0.9 is recommended, but > 0.8 is acceptable. ENCODE processed alignments file {ENCFF608YEA|/files/ENCFF608YEA/} processed by ChIP-seq ENCODE4 v1.8.0 GRCh38 pipeline was generated from a library with PBC1 value of 0.81. **audit\_warning**: PBC2 (PCR Bottlenecking Coefficient 2, M1/M2) is the ratio of the number of genomic locations where exactly one read maps uniquely (M1) to the number of genomic locations where two reads map uniquely (M2). A PBC2 value in the range 0 - 1 is severe bottlenecking, 1 - 3 is moderate bottlenecking, 3 - 10 is mild bottlenecking, > 10 is no bottlenecking. PBC2 value > 10 is recommended, but > 3 is acceptable. ENCODE processed alignments file {ENCFF608YEA|/files/ENCFF608YEA/} processed by ChIP-seq ENCODE4 v1.8.0 GRCh38 pipeline was generated from a library with PBC2 value of 5.33.' labels: reference_genome: hg38/genomes/GRCh38-hg38 accession: ENCSR932BNN status: released assay_term_name: ChIP-seq simple_biosample_summary: genetically modified (insertion) using CRISPR targeting H. sapiens ARID3A biosample_summary: Homo sapiens HepG2 genetically modified (insertion) using CRISPR targeting H. sapiens ARID3A replication_type: isogenic biosample_ontology: /biosample-types/cell_line_EFO_0001187/ perturbed: false doi: 10.17989/ENCSR932BNN date_created: '2021-10-18T20:50:07.406841+00:00' date_released: '2023-01-10' submitter_comment: '' target: ARID3A