-
Genetic Mechanisms of Disease Lab DAC
Dac
EGAC00001003416
-
Genetic Mechanisms of Disease Lab DAC
Dac
EGAC00001003417
-
Genetic Mechanisms of Disease Lab DAC
Dac
EGAC00001003425
-
Genetic Mechanisms of Disease Lab DAC
Dac
EGAC00001003427
-
DAC for "Integrated genetic analysis of primary CNS lymphoma"
Dac
EGAC00001003233
-
Dataset that contains runs of submission 161
Dataset
EGAD50000000253
-
Identification of genetic mutations characteristic for recurrence and metastasis of colon and rectal cancer.
Study
JGAS000091
-
Phylogenetic analysis of combined lobular and ductal carcinoma of the breast
Study
JGAS000300
-
Integrated Exome and RNA Sequencing of Dedifferentiated Liposarcoma
Study
JGAS000177
-
Mutational Spectrums and Clinical Features of Patients with LOXHD1 Variants Identified in a 8,074 Hearing Loss Patient Cohort.
Study
JGAS000192
-
Comprehensive genetic analysis of pediatric germ cell tumors
Study
JGAS000204
-
Target resequencing of LQTS-related 100 genes in Japanese patients
Study
JGAS000579
-
High-coverage whole-genome sequencing reveals structural variations in triple-negative breast cancer
Study
JGAS000095
-
DNA methylation array analysis of pediatric T-cell acute lymphoblastic leukemia
Study
JGAS000138
-
Whole-genome analysis of a healthy man with common trichromatic vision
Study
JGAS000348
-
Identification of the genes associated with EGFR-mutant lung cancer
Study
JGAS000129
-
Identification of RNA biomarkers in Parkinson's disease patients
Study
JGAS000119
-
Whole-exome sequencing of MDS and related myeloid neoplasms
Study
JGAS000023
-
Prevalence and Clinical Characteristics of hearing loss caused by MYH14 mutation
Study
JGAS000323
-
Comprehensive genomic analysis of patient derived orthotopic xenograft model in primary central nervous system lymphoma
Study
JGAS000178
-
CRISPR-screening identifies mechanisms of resistance to KRASG12C and SHP2 inhibitor combinations in non-small cell lung cancer
Study
JGAS000643
-
Comprehensive analyses of genetic aberrations in cholangiolocarcinoma
Study
JGAS000597
-
Next-generation sequencing-based comprehensive genetic analysis of undiagnosed disease
Study
JGAS000522
-
Rapid detection of expanded short tandem repeats in personal genomics using hybrid sequencing.
Study
JGAS000002
-
POU4F3 mutation screening in Japanese hearing loss patients.
Study
JGAS000093
-
Genetics of diffuse large B-cell lymphoma in Japan
Study
JGAS000307
-
Genetic alterations that deregulate RB and PDGFRA signaling pathways drive tumor progression in IDH2-mutant astrocytoma
Study
JGAS000646
-
Identification of genetic polymorphism on aggressive periodontitis
Study
JGAS000024
-
DNA demethylation is associated with malignant progression of low-grade gliomas
Study
JGAS000146
-
Targeted exome sequencing identify compound heterozygous TYK2 mutations in patients with primary immunodeficiency who developed EBV-associated lymphoma
Study
JGAS000098
-
Japanese Reference Genome JG1
Study
JGAS000259
-
Defined Lifestyle and Germline Factors Predispose Asian Populations to Gastric Cancer
Study
JGAS000228
-
mutation analysys of Gorlin syndrome
Study
JGAS000099
-
Analysis of mutational and proteomic heterogeneity of gastric cancer to monitor post-treatment tumor burden using circulating tumor DNA
Study
JGAS000231
-
Whole exome sequencing of familial MDS, Two patients
Study
JGAS000162
-
Development of the prevention and therapy of CRC using patient derived culture tissues.
Study
JGAS000139
-
C-MACH reduced-representation bisulfite sequencing (RRBS)
Study
JGAS000171
-
Development of a diagnostic gene panel for Gorlin syndrome and its application to liquid biopsy
Study
JGAS000308
-
Identification of responsible genes and development of standardized medicine for familial breast cancer by genetic analysis with NGS technology
Study
JGAS000224
-
Demographic History and Local Adaptation in Asian Population
Study
JGAS000238
-
Whole genome, whole exome and transcriptome sequencing of 10 ccRCC with Von Hippel-Lindau disease
Study
JGAS000544
-
An Organoid Biobank of Rare Human Neuroendocrine Neoplasms Enables Genotype-Phenotype Mapping
Study
JGAS000237
-
Reconstruction of the personal information from human genome reads in gut metagenome sequencing data
Study
JGAS000600
-
Elucidation of molecular mechanism of NAFLD-HCC
Study
JGAS000523
-
Inherited chromosomally-integrated human herpesvirus 6A/B (HHV-6A/B) genome sequences in the Japanese population
Study
JGAS000240
-
Genetic analysis in monozygotic twins discordant for bipolar disorder
Study
JGAS000014
-
Comprehansive analysis of somatic mutations and genetic variations with whole genome sequencing
Study
JGAS000516
-
Frequent post-treatment monitoring of colorectal cancer using individualized ctDNA validated by multi-regional molecular profiling
Study
JGAS000243
-
RNA-seq analysis of BMP-stimulated glioma initiating cells
Study
JGAS000077
-
Immunohistochemical and molecular pathological search in gastrointestinal tumors
Study
JGAS000538