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 |
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 |
JGAS00000000131
|
Chromatin remodeler CHD7 regulates the stem cell identity of human neural progenitors |
JGAS00000000132
|
Transcriptome analysis of Williams syndrome |
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 |
JGAS00000000146
|
DNA demethylation is associated with malignant progression of low-grade gliomas |
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 |
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 |
JGAS00000000182
|
Analysis of genomic alterations in dedifferentiated liposarcoma |
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. |
JGAS00000000203
|
Target sequencing of 8 hereditary prostate cancer genes in Japanese |
JGAS00000000205
|
Elucidation of disease state by multi-layered omics analysis |
JGAS00000000207
|
Epigenomic analysis of human androgenetic trophoblast stem cells derived from complete hydatidiform mole |