type: position_score table: filename: ENCFF640UMI.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_ENCSR722OTA column_index: 3 type: float desc: signal histogram: type: number number_of_bins: 100 meta: summary: 'ChIP-seq ENCSR722OTA [TISSUE: Homo sapiens WTC11 genetically modified (insertion) using CRISPR targeting H. sapiens NR3C1, TARGET: NR3C1]' description: '**status**: released **biological\_replicates**: Rep 1, Rep 2 **summary**: genetically modified (insertion) using CRISPR targeting H. sapiens NR3C1 **output\_type**: conservative IDR thresholded peaks **audit\_internal\_action**: Released analysis {ENCAN139LRC|/analyses/ENCAN139LRC/} has in progress subobject quality standard {encode4-tf-chip|/quality-standards/encode4-tf-chip/} **audit\_warning**: Processed alignments file {ENCFF743OZK|/files/ENCFF743OZK/} processed by ChIP-seq ENCODE4 v1.8.1 GRCh38 pipeline has 18916060 usable fragments. The minimum ENCODE standard for each replicate in a ChIP-seq experiment targeting NR3C1-human and investigated as a transcription factor is 10 million usable fragments. The recommended value is > 20 million, but > 10 million is acceptable. (See {ENCODE ChIP-seq data standards|/data-standards/chip-seq/} ) **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 {ENCFF743OZK|/files/ENCFF743OZK/} processed by ChIP-seq ENCODE4 v1.8.1 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 {ENCFF743OZK|/files/ENCFF743OZK/} processed by ChIP-seq ENCODE4 v1.8.1 GRCh38 pipeline was generated from a library with PBC2 value of 5.08. **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 {ENCFF667OJS|/files/ENCFF667OJS/} processed by ChIP-seq ENCODE4 v1.8.1 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 {ENCFF667OJS|/files/ENCFF667OJS/} processed by ChIP-seq ENCODE4 v1.8.1 GRCh38 pipeline was generated from a library with PBC2 value of 5.16.' labels: reference_genome: hg38/genomes/GRCh38-hg38 accession: ENCSR722OTA status: released assay_term_name: ChIP-seq simple_biosample_summary: genetically modified (insertion) using CRISPR targeting H. sapiens NR3C1 biosample_summary: Homo sapiens WTC11 genetically modified (insertion) using CRISPR targeting H. sapiens NR3C1 replication_type: isogenic biosample_ontology: /biosample-types/cell_line_EFO_0009747/ perturbed: false doi: 10.17989/ENCSR722OTA date_created: '2022-09-21T16:14:13.744489+00:00' date_released: '2023-01-06' submitter_comment: '' target: NR3C1