TF_ChIP-seq_ENCSR996SKD
TF_ChIP-seq ENCSR996SKD [biosample_summary="Homo sapiens K562 genetically modified (insertion) using CRISPR targeting H. sapiens CXXC5" and target="CXXC5"]
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| Id: | TF_ChIP-seq/ENCSR996SKD |
| Type: | position_score |
| Version: | 0 |
| Summary: |
TFChIP-seq ENCSR996SKD [biosamplesummary="Homo sapiens K562 genetically modified (insertion) using CRISPR targeting H. sapiens CXXC5" and target="CXXC5"] |
| Description: |
status: released biological_replicates: Rep 3, Rep 4 summary: genetically modified (insertion) using CRISPR targeting H. sapiens CXXC5 output_type: IDR thresholded peaks audit_internal_action: Released analysis {ENCAN941CNL|/analyses/ENCAN941CNL/} has in progress subobject quality standard {encode4-tf-chip|/quality-standards/encode4-tf-chip/} 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 {ENCFF727PGV|/files/ENCFF727PGV/} processed by ChIP-seq ENCODE4 v1.8.0 GRCh38 pipeline was generated from a library with NRF value of 0.71. 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 {ENCFF727PGV|/files/ENCFF727PGV/} processed by ChIP-seq ENCODE4 v1.8.0 GRCh38 pipeline was generated from a library with PBC1 value of 0.70. 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 {ENCFF727PGV|/files/ENCFF727PGV/} processed by ChIP-seq ENCODE4 v1.8.0 GRCh38 pipeline was generated from a library with PBC2 value of 3.18. 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 {ENCFF245SPQ|/files/ENCFF245SPQ/} processed by ChIP-seq ENCODE4 v1.8.0 GRCh38 pipeline was generated from a library with NRF value of 0.71. 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 {ENCFF245SPQ|/files/ENCFF245SPQ/} processed by ChIP-seq ENCODE4 v1.8.0 GRCh38 pipeline was generated from a library with PBC1 value of 0.70. 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 {ENCFF245SPQ|/files/ENCFF245SPQ/} processed by ChIP-seq ENCODE4 v1.8.0 GRCh38 pipeline was generated from a library with PBC2 value of 3.27. |
| Labels: |
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| ID | Type | Default annotation | Description | Histogram | Range |
|---|---|---|---|---|---|
| TF_ChIP-seq_ENCSR996SKD | float |
TF_ChIP-seq_ENCSR996SKD |
TF_ChIP-seq ENCSR996SKD [biosample_summary="Homo sapiens K562 genetically modified (insertion) using CRISPR targeting H. sapiens CXXC5" and target="CXXC5"]
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[18.9, 3.73e+03] |
| Filename | Size | md5 |
|---|---|---|
| ENCFF798LLI.bed.gz | 795.27 KB | 4ad71498ce87f2eb0d6b1c8407bee3ef |
| ENCFF798LLI.bed.gz.dvc | 100.0 B | 6e8d77be3af26192b6b1ea92aa57a769 |
| ENCFF798LLI.tabix.bed.gz | 568.17 KB | a1905d76dd2712dbd3279b5a33eddcb3 |
| ENCFF798LLI.tabix.bed.gz.dvc | 106.0 B | 0331b28add67820d0c8c1603c85b75ef |
| ENCFF798LLI.tabix.bed.gz.tbi | 196.62 KB | 4297d58e554186d1f3b536718bea7936 |
| ENCFF798LLI.tabix.bed.gz.tbi.dvc | 110.0 B | b9d46521322a0faa02c26ef392f6f064 |
| genomic_resource.yaml | 5.28 KB | 22a9074d10b19a7ead4065b7f9c24ba5 |
| genomic_resource_original.yaml | 5.12 KB | bb0e3cbf69ae3bfec91cdb583c4f3cdf |
| statistics/ |