NBDC Research ID: hum0312.v1
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SUMMARY
Aims: Genome-wide association studies (GWAS) have been conducted in multifactorial diseases such as autoimmune diseases, and more than 1000 disease susceptibility variants have been identified. However, GWAS only indicates the presence of disease-causing variants within a region. The effects of the accumulation of these variants on the functions of cells and tissues involved in disease states must be clarified. This study aims to integrate public GWAS data and expression quantitative trait loci (eQTL) and splicing QTL (sQTL) analyses to elucidate the pathogenesis of various multifactorial diseases through a comprehensive analysis of functional variants.
Methods: Total RNAs from Lymphoblastoid Cell line (LCL) samples were used for Iso-seq and RNA-seq analyses
Participants/Materials: Samples with and without interferon (IFNa2) stimulation were obtained from LCL samples derived from the 1000 Genomes Registry.
Dataset ID | Type of Data | Criteria | Release Date |
---|---|---|---|
NGS (Iso-seq) | Unrestricted-access | 2024/06/17 | |
NGS (RNA-seq) | Unrestricted-access | 2024/06/17 |
*When the research results including the data which were downloaded from NHA/DRA, are published or presented somewhere, the data user must refer the papers which are related to the data, or include in the acknowledgment. Learn more
MOLECULAR DATA
Participants/Materials |
2 healthy subjects DRA016394: 1 LCL sample with IFNa2 stimulation DRA018714: 2 LCL samples with and without IFNa2 stimulation (total 4 samples) |
Targets | Iso-seq |
Target Loci for Capture Methods | - |
Platform | PacBio [Sequel II/IIe] |
Library Source | Total RNA extracted from LCL samples |
Cell Lines | GM19078, GM12878 (Coriell Institute) |
Library Construction (kit name) | SMRTbell Express Template Prep Kit 3.0 |
Fragmentation Methods | - |
Spot Type | Single-end |
Read Length (without Barcodes, Adaptors, Primers, and Linkers) | - |
DDBJ Sequence Read Archive ID | |
Total Data Volume |
DRA016394: 4.6 GB (bam) DRA018714: 175.5 GB (bam) |
Comments (Policies) | NBDC policy |
Participants/Materials |
2 healthy subjects 4 LCL samples with and without IFNa2 stimulation (total 8 samples) |
Targets | RNA-seq |
Target Loci for Capture Methods | - |
Platform | Nanopore [MinION] |
Library Source | Total RNA extracted from LCL samples |
Cell Lines | GM19078, GM12878 (Coriell Institute) |
Library Construction (kit name) | SMART-seq v4 Ultra Low Input RNA Kit |
Fragmentation Methods | - |
Spot Type | Single-end |
Read Length (without Barcodes, Adaptors, Primers, and Linkers) | - |
DDBJ Sequence Read Archive ID | DRA016393 |
Total Data Volume | 335.5 GB (fastq) |
Comments (Policies) | NBDC policy |
Participants/Materials |
94 healthy subjects 94 LCL samples with IFNa2 stimulation 20 LCL samples without IFNa2 stimulation |
Targets | RNA-seq |
Target Loci for Capture Methods | - |
Platform | Illumina [NovaSeq 6000] |
Library Source | Total RNA extracted from LCL samples |
Cell Lines | 94 samples (Coriell Institute) |
Library Construction (kit name) | NEBNext UltraDirectional RNA Library Prep Kit |
Fragmentation Methods | Enzymatic fragmentation |
Spot Type | Paired-end |
Read Length (without Barcodes, Adaptors, Primers, and Linkers) | 150 bp |
DDBJ Sequence Read Archive ID | DRA016395 |
Total Data Volume | 335.5 GB (fastq) |
Comments (Policies) | NBDC policy |
DATA PROVIDER
Principal Investigator: Yuta Kochi
Affiliation: Department of Genomic Function and Diversity, Medical Research Institute, Tokyo Medical and Dental University
Project / Group Name: -
Funds / Grants (Research Project Number):
Name | Title | Project Number |
---|---|---|
KAKENHI Grant-in-Aid for Scientific Research (B) | Mechanisms of autoimmune disease pathogenesis through splicing QTLs in immune cells | 18H02849 |
KAKENHI Grant-in-Aid for Scientific Research (B) | Investigating the physiological and pathological significance of NMD target transcripts through transomics analysis | 22H02597 |
KAKENHI Grant-in-Aid for challenging Exploratory Research | Exploring the role of retroelements and their polymorphisms in autoimmune diseases | 21K19501 |
PUBLICATIONS
Title | DOI | Dataset ID | |
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1 | |||
2 |