type: position_score table: filename: ENCFF180BYN.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_ENCSR000EXP column_index: 3 type: float desc: 'TF_ChIP-seq ENCSR000EXP [biosample_summary="Homo sapiens erythroblast male" and target="GATA1"]' histogram: type: number number_of_bins: 100 meta: summary: 'TF_ChIP-seq ENCSR000EXP [biosample_summary="Homo sapiens erythroblast male" and target="GATA1"]' description: '**status**: released **biological\_replicates**: Rep 1, Rep 2 **summary**: male **output\_type**: optimal IDR thresholded peaks **audit\_internal\_action**: File {ENCFF180BYN|/files/ENCFF180BYN/} with status ''released'' is derived from file {ENCFF419RSJ|/files/ENCFF419RSJ/} with status ''archived''. **audit\_internal\_action**: Archived analysis {ENCAN003YUV|/analyses/ENCAN003YUV/} has in progress subobject quality standard {encode3-tf-chip|/quality-standards/encode3-tf-chip/} **audit\_not\_compliant**: Processed alignments file {ENCFF845AVW|/files/ENCFF845AVW/} processed by ChIP-seq ENCODE3 GRCh38 pipeline has 5748340 usable fragments. The minimum ENCODE standard for each replicate in a ChIP-seq experiment targeting GATA1-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\_not\_compliant**: Processed alignments file {ENCFF525TNI|/files/ENCFF525TNI/} processed by ChIP-seq ENCODE3 GRCh38 pipeline has 8451829 usable fragments. The minimum ENCODE standard for each replicate in a ChIP-seq experiment targeting GATA1-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\_not\_compliant**: 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 {ENCFF845AVW|/files/ENCFF845AVW/} processed by ChIP-seq ENCODE3 GRCh38 pipeline was generated from a library with PBC1 value of 0.45. **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 {ENCFF845AVW|/files/ENCFF845AVW/} processed by ChIP-seq ENCODE3 GRCh38 pipeline was generated from a library with NRF value of 0.51. **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 {ENCFF845AVW|/files/ENCFF845AVW/} processed by ChIP-seq ENCODE3 GRCh38 pipeline was generated from a library with PBC2 value of 1.51. **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 {ENCFF525TNI|/files/ENCFF525TNI/} processed by ChIP-seq ENCODE3 GRCh38 pipeline was generated from a library with NRF value of 0.64. **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 {ENCFF525TNI|/files/ENCFF525TNI/} processed by ChIP-seq ENCODE3 GRCh38 pipeline was generated from a library with PBC1 value of 0.61. **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 {ENCFF525TNI|/files/ENCFF525TNI/} processed by ChIP-seq ENCODE3 GRCh38 pipeline was generated from a library with PBC2 value of 2.30.' labels: reference_genome: hg38/genomes/GRCh38-hg38 accession: ENCSR000EXP status: released assay_term_name: ChIP-seq simple_biosample_summary: male biosample_summary: Homo sapiens erythroblast male replication_type: isogenic biosample_ontology: /biosample-types/primary_cell_CL_0000765/ perturbed: false doi: 10.17989/ENCSR000EXP date_created: '2014-02-12T23:15:34.419770+00:00' date_released: '2011-10-29' submitter_comment: '' target: GATA1