Dataset ID
JGAD000261
- Type of data
- NGS (WGS): RK067
- Access criteria
- Controlled-access (Type I)
- Total data volume
- 2.4 TB
- File formats
- FASTQ
- VCF
- XLSX
- Research
- hum0182
- Date published
- 2020-10-21
- Date modified
- 2021-04-19
- DDBJ Search
- JGAD000261 (opens in a new tab)
- JGA Study
- JGAS000180 (opens in a new tab)
Analysis method
WGS
- Materials and participants
- 1) RK067 (a liver cancer patient): 1 case
2) NA18943 (HapMap): 1 sample
4) RK014, RK019, RK020, RK067, RK085, RK0143, RK147, RK156, RK157, RK167, RK281 (liver cancer patients): 11 cases - Health statusMixed
- Subject count23 (Sample)
- CohortHapMap
- PopulationJapanese
- Sample description
- 1) DNA extracted from blood sample (normal cell) of a liver cancer patient
2) HapMap DNA sample
4) RK014, RK019, RK020, RK085, RK0143, RK147, RK156, RK157, RK167, RK281: DNA extracted from blood samples (normal cell) of liver cancer patients
RK014, RK019, RK020, RK067, RK085, RK0143, RK147, RK156, RK157, RK167, RK281: DNA extracted from tumor tissues of liver cancer patients - TissuePeripheral blood
- Tumor / normalMixed
- Cell line
- NA18943
- Experimental method
- WGS
- Target
- N/A
- Reagent kit
- Ligation Sequencing Kit (SQK-LSK108)
- Fragmentation
- g-TUBE (Covaris)
- Platform
- Oxford Nanopore Technologies MinION
- Read type
- Single-end
- Read length
- 7463 bp (①④)
3479 bp (②) - Data use policy
- NBDC data sharing policy (JGAP000001)
WGS
- Materials and participants
- 3) RK001-RK338 (liver cancer patients): 174 cases
- Health statusAffected
- Subject count174 (Individual)
- PopulationJapanese
- Sample description
- DNA extracted from blood sample (normal cell) of liver cancer patients
- TissuePeripheral blood
- Tumor / normalNormal
- Sample provider
- N/A
- Experimental method
- WGS
- Target
- N/A
- Reagent kit
- Paired-End DNA Sample Prep Kit
TruSeq DNA Sample Prep Kit
TruSeq Nano DNA Library Prep Kit - Fragmentation
- Ultrasonic fragmentation (Covaris)
- Platform
- Illumina Genome Analyzer IIx
Illumina HiSeq 2000 - Read type
- Paired-end
- Read length
- 100 bp
- Reference genome
- GRCh37
- Mapping
- bwa
- Read deduplication
- Picard
- QC and filtering
- N/A
- Analysis method
- VCMM (Shigemizu et al. Sci Rep (2013))
- Coverage (depth)
- 30x
- Variant count
- 4378
5,239,921 - Data use policy
- NBDC data sharing policy (JGAP000001)