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Dataset ID

JGAD000059

Type of data
NGS (RNA-seq)
Methylation array
Access criteria
Controlled-access (Type I)
Total data volume
330 GB
File formats
  • FASTQ
  • TXT
Research
hum0055
Date published
2020-09-28
Date modified
2024-01-19

Analysis method

RNA-seq

Materials and participants
Human liver tissues from NAFLD patients: 60 samples
  • Health status
    Affected
  • Subject count
    60 (Sample)
Sample description
mRNAs extracted from NAFLD liver tissues
  • Tissue
    Liver
  • Tumor / normal
    Normal
Sample provider
N/A
Experimental method
RNA-seq
Target
N/A
Reagent kit
SureSelect XT RNA Target Enrichment
Fragmentation
chemical fragmentation
Platform
Illumina HiSeq 2500
Read type
Paired-end
Read length
100 bp

メチル化アレイ

Materials and participants
Human liver tissues from NAFLD patients: 60 samples (56 are same samples as RNA-seq)
  • Health status
    Affected
  • Subject count
    60 (Sample)
Sample description
DNAs extracted from NAFLD liver tissues
  • Tissue
    Liver
  • Tumor / normal
    Normal
Sample provider
N/A
Experimental method
Methylation array
Target
N/A
Reagent kit
EZ DNA Methylation Kit
Infinium HumanMethylation450 BeadChip Kit
Platform
Illumina Infinium HumanMethylation450
Reference genome
GRCh37
QC and filtering
Probes as shown below were excluded:
with intensities indistinguishable from the background (detection P-value > 0.05) in more than one sample
with a bead count < 3 in at least 5 % of samples
including any SNPs
cross-reactive
Normalization
Raw DNA methylation data were preprocessed by normalizing to appropriate internal control probes. The effects of two types of CpG probes on CpG methylation measurements were corrected using beta-mixture quantile normalization, and batch effects were corrected using a ComBat normalization method in the R/Bioconductor package ChAMP.
Analysis method
GenomeStudio Software (Illumina)
Probe count
431,736 (CpGs on autosomes)