NBDC Research ID: hum0312.v2

 

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:

[DRA016393 / DRA016394 / DDRA016395 / RA018714] Total RNAs from Lymphoblastoid Cell line (LCL) samples were used for Iso-seq and RNA-seq analyses

[DRA016285] Twenty-nine immune cell subsets were isolated from peripheral blood mononuclear cells using the 14-color cell sorter BD FACSAria Fusion. Total RNA was extracted, followed by polyA selection and cDNA library preparation using the SMART-seq v4 Ultra Low Input RNA Kit and SQK-LSK109 for cDNA library preparation. For flow cytometry staining panels, the definitions of the Human Immunology Project were followed. Neutrophils were recovered with EasySep Direct Human Neutrophil Isolation Kits or MACSxpress Neutrophil Isolation Kits human. The generated cDNA was sequenced by Flongle Flow Cell (long-read system).

Participants/Materials: 

[DRA016393 / DRA016394 / DDRA016395 / RA018714] Samples with and without interferon (IFNa2) stimulation were obtained from LCL samples derived from the 1000 Genomes Registry.

[DRA016285] 29 immune cell types isolated from peripheral blood cells collected from a 42-year-old healthy individual

URL: https://www.tmd.ac.jp/english/press-release/20240528-3/

 

 

Dataset IDType of DataCriteriaRelease Date

DRA016394

DRA018714

NGS (Iso-seq) Unrestricted-access 2024/06/17

DRA016393

DRA016395

NGS (RNA-seq) Unrestricted-access 2024/06/17
DRA016285 NGS (RNA-seq) Unrestricted-access 2024/06/20

*Release Note

*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

DRA016394 / DRA018714

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

DRA016394

DRA018714

Total Data Volume

DRA016394: 4.6 GB (bam)

DRA018714: 175.5 GB (bam)

Comments (Policies) NBDC policy

 

DRA016393

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

 

DRA016395

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

 

DRA016285

Participants/Materials 1 healthy subject
Targets RNA-seq
Target Loci for Capture Methods -
Platform Nanopore [MinION]
Library Source Total RNAs extracted from 29 immune cell subsets
Cell Lines -
Library Construction (kit name)

SMART-seq v4 Ultra Low Input RNA Kit

SQK-LSK109

Fragmentation Methods -
Spot Type Single-end
Read Length (without Barcodes, Adaptors, Primers, and Linkers) -
DDBJ Sequence Read Archive ID DRA016285
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: TRAnscriptomic resource of Immune cells using Long-read Sequencing (TRAILS)

URL: https://www.tmd.ac.jp/english/press-release/20240528-3/

Funds / Grants (Research Project Number):

NameTitleProject 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
KAKENHI Grant-in-Aid for JSPS Fellows Elucidation of Sjögren's syndrome pathogenesis through retrotransposon sequences 21J00596
KAKENHI Grant-in-Aid for JSPS Fellows Development of high-depth Isoformics techniques and creation of a spatiotemporal protein atlas 21J15131
KAKENHI Grant-in-Aid for Scientific Research (B) Large-scale proteoform analysis for unveiling the entire view 21H02459

 

PUBLICATIONS

TitleDOIDataset ID
1 Long-read sequencing for 29 immune cell subsets reveals disease-linked isoforms doi: 10.1038/s41467-024-48615-4 DRA016285
2