type: position_score table: filename: ENCFF830TFU.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_ENCSR637QAM column_index: 3 type: float desc: 'TF_ChIP-seq ENCSR637QAM [biosample_summary="Homo sapiens GM12878" and target="TRIM22"]' histogram: type: number number_of_bins: 100 meta: summary: 'TF_ChIP-seq ENCSR637QAM [biosample_summary="Homo sapiens GM12878" and target="TRIM22"]' 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**: File {ENCFF830TFU|/files/ENCFF830TFU/} with status 'released'\ \ is derived from file {ENCFF419RSJ|/files/ENCFF419RSJ/} with status 'archived'.\n\ \n**audit\\_internal\\_action**: Archived analysis {ENCAN278XBJ|/analyses/ENCAN278XBJ/}\ \ has in progress subobject quality standard {encode3-tf-chip|/quality-standards/encode3-tf-chip/}\n\ \n**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 {ENCFF559OOA|/files/ENCFF559OOA/}\ \ processed by ChIP-seq ENCODE3 GRCh38 pipeline was generated from a library with\ \ NRF value of 0.71.\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 {ENCFF559OOA|/files/ENCFF559OOA/} processed\ \ by ChIP-seq ENCODE3 GRCh38 pipeline was generated from a library with PBC1 value\ \ of 0.70.\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 {ENCFF559OOA|/files/ENCFF559OOA/} processed by ChIP-seq ENCODE3 GRCh38\ \ pipeline was generated from a library with PBC2 value of 3.16.\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\ \ {ENCFF083LQR|/files/ENCFF083LQR/} processed by ChIP-seq ENCODE3 GRCh38 pipeline\ \ was generated from a library with PBC1 value of 0.82.\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 {ENCFF083LQR|/files/ENCFF083LQR/}\ \ processed by ChIP-seq ENCODE3 GRCh38 pipeline was generated from a library with\ \ PBC2 value of 5.50." labels: reference_genome: hg38/genomes/GRCh38-hg38 accession: ENCSR637QAM status: released assay_term_name: ChIP-seq simple_biosample_summary: '' biosample_summary: Homo sapiens GM12878 replication_type: isogenic biosample_ontology: /biosample-types/cell_line_EFO_0002784/ perturbed: false doi: 10.17989/ENCSR637QAM date_created: '2014-05-14T00:06:06.127112+00:00' date_released: '2014-07-07' submitter_comment: '' target: TRIM22