type: position_score
table:
  filename: ENCFF864GBH.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: DNase-seq_ENCSR000EQG
  column_index: 3
  type: float
  desc: 'DNase-seq ENCSR000EQG [biosample_summary="Homo sapiens T-helper 2 cell"]'
  histogram:
    type: number
    number_of_bins: 100
meta:
  summary: 'DNase-seq ENCSR000EQG [biosample_summary="Homo sapiens T-helper 2 cell"]'
  description: "**status**: released\n\n**biological\\_replicates**: Rep 2\n\n**summary**:\
    \ \n\n**output\\_type**: peaks\n\n**audit\\_error**: Alignment file {ENCFF272GJL|/files/ENCFF272GJL/}\
    \ processed by DNase-seq ENCODE4 v3.0.0-alpha.2 GRCh38 pipeline ( {ENCPL848KLD|/pipelines/ENCPL848KLD/}\
    \ ) for GRCh38 assembly has 18880967 mapped reads. According to ENCODE standards,\
    \ conventional DNase-seq profile requires a minimum of 20 million uniquely mapped\
    \ reads to generate a reliable SPOT (Signal Portion of Tags) score. The recommended\
    \ value is > 50 million. For deep, foot-printing depth DNase-seq 150-200 million\
    \ uniquely mapped reads are recommended. (See {ENCODE DNase-seq data standards|/data-standards/dnase-seq-encode4/})"
  labels:
    reference_genome: hg38/genomes/GRCh38-hg38
    accession: ENCSR000EQG
    status: released
    assay_term_name: DNase-seq
    simple_biosample_summary: ''
    biosample_summary: Homo sapiens T-helper 2 cell
    replication_type: isogenic
    biosample_ontology: /biosample-types/primary_cell_CL_0000546/
    perturbed: false
    doi: 10.17989/ENCSR000EQG
    date_created: '2013-12-12T07:10:07.137020+00:00'
    date_released: '2012-07-23'
    submitter_comment: 'Fastq file ENCFF001EKN contains reads of mixed lengths. Read
      lengths followed by respective number of reads: (28, 39855129), (36, 8250998)'
