type: position_score table: filename: ENCFF710IEF.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_ENCSR145TSJ column_index: 3 type: float desc: 'TF_ChIP-seq ENCSR145TSJ [biosample_summary="Homo sapiens K562" and target="ATF4"]' histogram: type: number number_of_bins: 100 meta: summary: 'TF_ChIP-seq ENCSR145TSJ [biosample_summary="Homo sapiens K562" and target="ATF4"]' description: "**status**: released\n\n**biological\\_replicates**: Rep 1, Rep 2\n\ \n**summary**: \n\n**output\\_type**: optimal IDR thresholded peaks\n\n**audit\\\ _internal\\_action**: Archived analysis {ENCAN117QJU|/analyses/ENCAN117QJU/} has\ \ in progress subobject quality standard {encode3-tf-chip|/quality-standards/encode3-tf-chip/}\n\ \n**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 {ENCFF676XEB|/files/ENCFF676XEB/} processed by ChIP-seq ENCODE3 hg19 pipeline\ \ was generated from a library with PBC1 value of 0.88.\n\n**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 {ENCFF676XEB|/files/ENCFF676XEB/}\ \ processed by ChIP-seq ENCODE3 hg19 pipeline was generated from a library with\ \ PBC2 value of 8.42.\n\n**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 {ENCFF258YDE|/files/ENCFF258YDE/} processed\ \ by ChIP-seq ENCODE3 hg19 pipeline was generated from a library with PBC1 value\ \ of 0.88.\n\n**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 {ENCFF258YDE|/files/ENCFF258YDE/} processed by ChIP-seq ENCODE3 hg19 pipeline\ \ was generated from a library with PBC2 value of 8.14." labels: reference_genome: hg38/genomes/GRCh38-hg38 accession: ENCSR145TSJ status: released assay_term_name: ChIP-seq simple_biosample_summary: '' biosample_summary: Homo sapiens K562 replication_type: isogenic biosample_ontology: /biosample-types/cell_line_EFO_0002067/ perturbed: false doi: 10.17989/ENCSR145TSJ date_created: '2015-06-30T21:09:18.667484+00:00' date_released: '2018-01-26' submitter_comment: We note that this ChIP-seq experiment was performed using an antibody for which we have provided a compliant primary characterization but no secondary characterization. A secondary characterization using IP-MS was attempted, but the experiment failed. There is no remaining antibody from this lot number and therefore additional secondary characterizations cannot be attempted. However, because the replicate ChIP-seq datasets passed the ENCODE IDR ChIP-seq data quality standards, we are releasing the data to the public. target: ATF4