Study List

Studies
Accession Title
JGAS00000000001 Identification and Characterization of Cancer Mutations in Japanese LungAdenocarcinoma without Sequencing of Normal Tissue Counterparts
JGAS00000000002 Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing.
JGAS00000000004 Genomic and Genetic Analysis of Brain Tumors and Analysis of Their Clinicopathological Significance
JGAS00000000005 Gene expression of human Th17 cells before and after activation
JGAS00000000006 DNA methylation dynamics during early human development
JGAS00000000007 Research for genetic causes and mechanisms of Hirschsprung's or Hirschsprung's related diseases
JGAS00000000008 Research for candidate genes of splenic epidermoid cyst
JGAS00000000009 Whole exome sequence analysis in multiple system atrophy
JGAS00000000011 Systematic identification of long non-coding RNAs potentially involved in gastrointestinal carncer
JGAS00000000012 Genotype data from Nagahama cohort project
JGAS00000000013 Whole exome sequence analysis in sporadic amyotrophic lateral sclerosis
JGAS00000000014 Genetic analysis in monozygotic twins discordant for bipolar disorder
JGAS00000000015 DNA methylation at HBV integrants and flanking host genomes
JGAS00000000016 Genetic analysis in lifestyle-related disease, arteriosclerotic disease, and aging-related diseases.
JGAS00000000017 Leukemic evolution of donor-derived cells harboring IDH2 and DNMT3A mutations after allogeneic stem cell transplantation
JGAS00000000018 An imputation reference panel of HLA variants in Japanese
JGAS00000000021 Genomics characterization of primary central nervous system lymphoma
JGAS00000000022 Integrated copy number and expression analysis identifies profiles of whole-arm chromosomal alterations and subgroups with favorable outcome in ovarian clear cell carcinomas
JGAS00000000023 Whole-exome sequencing of MDS and related myeloid neoplasms
JGAS00000000024 Identification of genetic polymorphism on aggressive periodontitis
JGAS00000000025 TEST1
JGAS00000000026 Epigenome mapping in purified cells of the digestive and urogenital organs: Participation in International Human Epigenome Consortium (IHEC) (WGBS)
JGAS00000000027 Epigenome mapping in purified cells of the digestive and urogenital organs: Participation in International Human Epigenome Consortium (IHEC) (ChIP-seq)
JGAS00000000028 Epigenome mapping in purified cells of the digestive and urogenital organs: Participation in International Human Epigenome Consortium (IHEC) (RNA-Seq)
JGAS00000000032 Effective screening strategy for deafness using a new-genetation sequencing platform: a consecutive analysis
JGAS00000000035 Searching for rare/low frequency variants in rheumatoid arthritis by exome sequencing
JGAS00000000036 Whole-exome sequencing of pediatric solid tumors
JGAS00000000037 Development of molecular targeted therapy for small cell lung cancer by comprehensive genome analysis
JGAS00000000038 Parent-of-origin dependent DNA methylation and gene expression in the human placenta
JGAS00000000039 Analysis of TKI resistant mechanism for gastrointstinal stromal tumor
JGAS00000000040 Identification of genetic polymorphism on aggressive periodontitis
JGAS00000000041 Genetic analysis in an inherited cardiac arrhythmia
JGAS00000000042 Constructing database of magnetic resonance imaging of the brain and the ancillary clinical information for multisite collaboration studies: a dataset from normal individuals
JGAS00000000043 Constructing database of magnetic resonance imaging of the brain and the ancillary clinical information for multisite collaboration studies: a dataset from Schizophrenia individuals
JGAS00000000044 Constructing database of magnetic resonance imaging of the brain and the ancillary clinical information for multisite collaboration studies: a dataset from Depression individuals
JGAS00000000045 Constructing database of magnetic resonance imaging of the brain and the ancillary clinical information for multisite collaboration studies: a dataset from Bipolar disorder individuals
JGAS00000000046 Genome-wide copy number analysis of neuroblastoma
JGAS00000000047 Transcriptome analysis of adolescents and young adults with Acute Lymphoblastic Leukemia
JGAS00000000051 Japanese Alzheimer's disease neuroimaging initiative
JGAS00000000052 Research of factors related to diagnosis, progression, prognosis and treatment of hepato-biliary-pancreatic malignancies
JGAS00000000053 Transcriptome analysis of Hepatitis B for drug discovery and clinical applications
JGAS00000000054 TEST2
JGAS00000000057 Homozygous inactivation of CHEK2 is linked to a familial case of multiple primary lung cancer with accompanying cancers in other organs
JGAS00000000059 Genetic and epigentic analysis of non-alcoholic fatty liver disease. Methylation analysis of nonalcoholic fatty liver.
JGAS00000000060 Investigating genomic intratumor heterogeneity in colorectal carcinoma
JGAS00000000061 Geriatric Oncology Database of genotypes and methylation, gene expression, clinical data, and survey results on psychosocial and physical conditions in Japanese elderly cancer patients to establish truly effective treatment strategy
JGAS00000000062 Identification of new molecular targets with profiling of malignant mesothelioma
JGAS00000000064 RNA expression profiling of neuromuscular diseases and viral diseases
JGAS00000000065 Sequencing cancer mutations in various types of lung cancer using the long-read, portable sequencer
JGAS00000000070 CAGE analysis for non-small cell lung carcinoma
JGAS00000000073 Epigenomic analysis of the human placenta and endometrium constituting the fetal-maternal interface
JGAS00000000075 Intractable Cancer Therapy Development through a New Target Identification by Molecular Profiling
JGAS00000000076 Project for Development of Innovative Research on Cancer Therapeutics; Identifiying the predictive factors for response to chemoherapy in ovarian cancer
JGAS00000000077 RNA-seq analysis of BMP-stimulated glioma initiating cells
JGAS00000000078 Standard epigenome mapping in human epithelial cells of the digestive and urogenital organs [BS-Seq ]
JGAS00000000079 Standard epigenome mapping in human epithelial cells of the digestive and urogenital organs [ ChIP-Seq ]
JGAS00000000080 Standard epigenome mapping in human epithelial cells of the digestive and urogenital organs [RNA-Seq ]
JGAS00000000085 Expression quantitative trait loci analysis using human immune cells in a Japanese population
JGAS00000000086 Identification of genetic mutations characteristic for recurrence and metastasis of gastric cancer.
JGAS00000000087 Identification of genetic mutations characteristic for recurrence and metastasis of lymphoma.
JGAS00000000088 Genome-wide integrative analysis of pediatric pancreatoblastoma
JGAS00000000089 Project for Development of Innovative Research on Cancer Therapeutics;Shuttle system between petient-derived xenograft and ex vivo culture for innovative platform of evaluating drug sensitivity.
JGAS00000000090 Whole transcriptome sequencing of pediatric T-cell acute lymphoblastic leukemia
JGAS00000000091 Identification of genetic mutations characteristic for recurrence and metastasis of colon and rectal cancer.
JGAS00000000092 intratumor heterogeneity in colorectal adenoma and carcinoma
JGAS00000000093 POU4F3 mutation screening in Japanese hearing loss patients.
JGAS00000000094 The elucidation of molecular mechanisms of hematopoietic stem cells focusing on paroxysmal nocturnal hemoglobinuria (PNH)-type cells
JGAS00000000095 High-coverage whole-genome sequencing reveals structural variations in triple-negative breast cancer
JGAS00000000096 WGS analysis of a glioma initiating cell line
JGAS00000000098 Targeted exome sequencing identify compound heterozygous TYK2 mutations in patients with primary immunodeficiency who developed EBV-associated lymphoma
JGAS00000000099 mutation analysys of Gorlin syndrome
JGAS00000000101 GWAS for atrial fibrillation in the Japanese population
JGAS00000000103 Global Architecture of anti-Tumor B-Cell Immunity against Gastric Cancer
JGAS00000000104 Identification of genetic mutations characteristic for recurrence of serous ovarian cancer.
JGAS00000000105 High-coverage whole exome sequence in non-TRU-type lung adenocarcinomas
JGAS00000000106 Molecular analysis of diffuse cerebellar gliomas
JGAS00000000107 Epigenomic analysis of the human placenta and endometrium constituting the fetal-maternal interface
JGAS00000000108 Genomic DNA analysis for malignant mesothelioma from the patients of Japan and USA.
JGAS00000000109 Genome sequencing of biliary tract cancers
JGAS00000000111 Searching for DNA methylation sites associated with panic disorder
JGAS00000000112 Epigenome analysis of human trophoblast stem cells
JGAS00000000113 Comprehensive genomic analysis of colorectal cancer with microsatellite instability
JGAS00000000114 Biobank Japan genotype and phenotype data
JGAS00000000115 BHD-associated kidney cancer
JGAS00000000119 Identification of RNA biomarkers in Parkinson's disease patients
JGAS00000000120 419 Japanese healthy control
JGAS00000000121 Controlling cell differentiation with precision through understanding the structure and dynamics of gene regulatory networks
JGAS00000000123 WFS1 mutation screening in a large series of Japanese hearing loss patients: Massively parallel DNA sequencing-based analysis
JGAS00000000124 CAGE analysis for endometrial carcinoma
JGAS00000000125 Neuron-specifc methylome analysis of Alzheimer's disease brain
JGAS00000000126 Genome-wide analysis for non alcoholic fatty liver disease
JGAS00000000127 Innate myeloid cell sbuset-specific gene expression patterns in the human colon are altered in Crohn's disease patients
JGAS00000000129 Identification of the genes associated with EGFR-mutant lung cancer
JGAS00000000130 Molecular Profiling and Sequential Somatic Mutation Shift in Hypermutator Tumors Harboring POLE Mutations
JGAS00000000131 Chromatin remodeler CHD7 regulates the stem cell identity of human neural progenitors
JGAS00000000132 Transcriptome analysis of Williams syndrome
JGAS00000000134 Clonal structure and oncogenic potential of liver cirrhosis tissues.
JGAS00000000135 Treg cell subset-specific gene expression patterns in human head and neck cancer
JGAS00000000136 Research for drug discovery and elucidation of pathophysiology using disease-specific iPS cells
JGAS00000000137 Whole genome sequencing and mutation rate analysis of Vietnamese trios with paternal dioxin exposure
JGAS00000000138 DNA methylation array analysis of pediatric T-cell acute lymphoblastic leukemia
JGAS00000000140 Target sequencing of 11 hereditary breast cancer genes in Japanese
JGAS00000000141 Global Architecture of anti-Tumor B-Cell Immunity against Gastric Cancer
JGAS00000000144 A multicenter study of susceptibility genes to type 1 diabetes
JGAS00000000145 Naïve Treg-specific genomic DNA hypomethylation for autoimmune disease susceptibility
JGAS00000000146 DNA demethylation is associated with malignant progression of low-grade gliomas
JGAS00000000147 Transcriptome sequencing, DNA methylation analysis, and SNP array analysis of acute lymphoblastic leukemia in Down syndrome
JGAS00000000149 The exploratory research of diagnositic biomarker and therapeutic targets of renal cell carcinoma.
JGAS00000000150 Genetic and transcriptional landscape of plasma cells in POEMS syndrome
JGAS00000000151 WGS analysis of Japanese liver cancer
JGAS00000000153 Gene expression analysis for nasal polyps
JGAS00000000155 Whole genome sequencing analysis of esophageal squamous cell carcinoma
JGAS00000000158 Prediction of response to preoperative chemoradiotherapy in rectal cancer based on whole-exome sequencing and transcriptomic analysis
JGAS00000000159 3.5KJPNv2, an allele frequency panel of 3,552 Japanese individuals
JGAS00000000160 Susceptibility loci for tanning ability in Japanese population identified by genome-wide association study
JGAS00000000162 Whole exome sequencing of familial MDS, Two patients
JGAS00000000164 Comprehensive assay for the molecular profiling of cancer by target enrichment from formalin-fixed paraffin-embedded specimens
JGAS00000000166 OTOF mutation analysis with massively parallel DNA sequencing in 2,265 Japanese sensorineural hearing loss patients.
JGAS00000000169 Whole exome sequencing of uterine adenomyosis
JGAS00000000171 C-MACH reduced-representation bisulfite sequencing (RRBS)
JGAS00000000172 Comprehensive sequencing analyses of uterine and ovarian carcinosarcoma
JGAS00000000174 Development of actionable molecular targets and/or biomarkers for prognostication and patient stratification in gynecological cancer based on whole-exome sequencing and epigenomic analysis
JGAS00000000176 Genomic Structural Variants in Japanese Malignant mesothelioma patients
JGAS00000000177 Integrated Exome and RNA Sequencing of Dedifferentiated Liposarcoma
JGAS00000000178 Comprehensive genomic analysis of patient derived orthotopic xenograft model in primary central nervous system lymphoma
JGAS00000000179 Identification of driver oncogenes in scirrhous-type gastric cancer cell lines
JGAS00000000180 Nanopore whole-genome sequencing of sample RK067 and variant-call data (SNVs and intermediate-sized deletions) of 174 Japanese samples.
JGAS00000000182 Analysis of genomic alterations in dedifferentiated liposarcoma
JGAS00000000186 Shotgun metagenome sequencing of saliva samples using PromethION
JGAS00000000188 Integrated multi-omics analysis of pediatric hepatoblastoma
JGAS00000000189 Target sequencing of ROS1-rearranged lung cancer patients
JGAS00000000191 CLDN14 mutation identifed from Japanese sensorineural hearing loss patient.
JGAS00000000192 Mutational Spectrums and Clinical Features of Patients with LOXHD1 Variants Identified in a 8,074 Hearing Loss Patient Cohort.
JGAS00000000194 Viral integration analysis of hepatocellular carcinoma using virus capture sequence.
JGAS00000000197 Whole-genome bisulfite sequencing for high-grade glioma
JGAS00000000198 Identification of therapeutic target molecules for prostate cancer by using next generation sequencer
JGAS00000000199 Somatic inflammatory gene mutations accumulate in human ulcerative colitis epithelium
JGAS00000000203 Target sequencing of 8 hereditary prostate cancer genes in Japanese
JGAS00000000205 Elucidation of disease state by multi-layered omics analysis
JGAS00000000206 Establishment of an integrated database for clinical and genomic data in cancer
JGAS00000000207 Epigenomic analysis of human androgenetic trophoblast stem cells derived from complete hydatidiform mole
JGAS00000000211 Elucidation of genomic pathology of a patient with concurrent acute myeloid leukemia and mediastinal germ cell tumor
JGAS00000000214 comprehensive genetic analysis and database construction for head and neck cancer
JGAS00000000216 Whole exome sequencing of surgically resected lung adenocarcinomas and gastric adenocarcinomas.
JGAS00000000217 Sequence analysis of colorectal serrated lesions
JGAS00000000218 Expression profiling of Gorlin iPSCs in the osteoblast induction culture
JGAS00000000221 The genetic analysis of circulating tumor DNA in blood of the digestive cancer patients to investigate the prognostic factors of metastasis and reccurence.
JGAS00000000222 Ten colorectal cancer patients with locally advanced primary tumors who underwent primary tumor resection following neoadjuvant chemotherapy (NAC).
JGAS00000000223 Influence of pre-analytical processing on blood protein profiles (AMED-Metabolites)
JGAS00000000224 Identification of responsible genes and development of standardized medicine for familial breast cancer by genetic analysis with NGS technology
JGAS00000000226 Mortality and risk of progression to adult T-cell leukemia/lymphoma in patients with HTLV-1-associated myelopathy/tropical spastic paraparesis
JGAS00000000230 Identification and characterization of molecular markers in aging and neuronal disorders
JGAS00000000231 Analysis of mutational and proteomic heterogeneity of gastric cancer to monitor post-treatment tumor burden using circulating tumor DNA
JGAS00000000240 Inherited chromosomally-integrated human herpesvirus 6A/B (HHV-6A/B) genome sequences in the Japanese population
JGAS00000000241 Genomic profiling identified ERCC2 helicase domain mutations respond to platinum-based neoadjuvant therapy in urothelial bladder cancer