type: position_score table: filename: ENCFF867MAL.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_ENCSR000DRN column_index: 3 type: float desc: signal histogram: type: number number_of_bins: 100 meta: summary: 'ChIP-seq ENCSR000DRN [TISSUE: Homo sapiens GM12872, TARGET: CTCF]' description: "**status**: released\n\n**biological\\_replicates**: Rep 1, Rep 2,\ \ Rep 3\n\n**summary**: \n\n**output\\_type**: IDR thresholded peaks\n\n**audit\\\ _internal\\_action**: Released analysis {ENCAN775MGQ|/analyses/ENCAN775MGQ/} has\ \ in progress subobject document {aa2c3e73-a85f-4a55-ac45-1069ac3e0371|/documents/aa2c3e73-a85f-4a55-ac45-1069ac3e0371/}\n\ \n**audit\\_internal\\_action**: Released analysis {ENCAN775MGQ|/analyses/ENCAN775MGQ/}\ \ has in progress subobject quality standard {encode4-tf-chip|/quality-standards/encode4-tf-chip/}\n\ \n**audit\\_not\\_compliant**: Processed alignments file {ENCFF789ESG|/files/ENCFF789ESG/}\ \ processed by ChIP-seq ENCODE4 v1.5.1 GRCh38 pipeline has 9908172 usable fragments.\ \ The minimum ENCODE standard for each replicate in a ChIP-seq experiment targeting\ \ CTCF-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/} )\n\n**audit\\_warning**:\ \ Processed alignments file {ENCFF466NQR|/files/ENCFF466NQR/} processed by ChIP-seq\ \ ENCODE4 v1.5.1 GRCh38 pipeline has 10013676 usable fragments. The minimum ENCODE\ \ standard for each replicate in a ChIP-seq experiment targeting CTCF-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/} )\n\n**audit\\_warning**: Processed\ \ alignments file {ENCFF928CUP|/files/ENCFF928CUP/} processed by ChIP-seq ENCODE4\ \ v1.5.1 GRCh38 pipeline has 15543973 usable fragments. The minimum ENCODE standard\ \ for each replicate in a ChIP-seq experiment targeting CTCF-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/} )\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 {ENCFF789ESG|/files/ENCFF789ESG/} processed by ChIP-seq ENCODE4 v1.5.1\ \ GRCh38 pipeline was generated from a library with NRF value of 0.75.\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\ \ {ENCFF789ESG|/files/ENCFF789ESG/} processed by ChIP-seq ENCODE4 v1.5.1 GRCh38\ \ pipeline was generated from a library with PBC1 value of 0.75.\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 {ENCFF789ESG|/files/ENCFF789ESG/}\ \ processed by ChIP-seq ENCODE4 v1.5.1 GRCh38 pipeline was generated from a library\ \ with PBC2 value of 3.81.\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 {ENCFF928CUP|/files/ENCFF928CUP/} processed by ChIP-seq ENCODE4 v1.5.1\ \ GRCh38 pipeline was generated from a library with NRF value of 0.80.\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\ \ {ENCFF928CUP|/files/ENCFF928CUP/} processed by ChIP-seq ENCODE4 v1.5.1 GRCh38\ \ pipeline was generated from a library with PBC1 value of 0.81.\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 {ENCFF928CUP|/files/ENCFF928CUP/}\ \ processed by ChIP-seq ENCODE4 v1.5.1 GRCh38 pipeline was generated from a library\ \ with PBC2 value of 5.44." labels: reference_genome: hg38/genomes/GRCh38-hg38 accession: ENCSR000DRN status: released assay_term_name: ChIP-seq simple_biosample_summary: '' biosample_summary: Homo sapiens GM12872 replication_type: isogenic biosample_ontology: /biosample-types/cell_line_EFO_0001159/ perturbed: false doi: 10.17989/ENCSR000DRN date_created: '2013-12-12T06:56:50.885873+00:00' date_released: '2011-03-17' submitter_comment: Replicate 3,1 of this experiment was previously attributed to biosample ENCBS216AAA and replicate 2,1 of this experiment was previously attributed to biosample ENCBS216AAA but they have since been corrected to the current biosamples. Please note that the biosample term has remain unchanged. target: CTCF