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Targeted exome sequencing identify compound heterozygous TYK2 mutations in patients with primary immunodeficiency who developed EBV-associated lymphoma
Study
JGAS000098
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mutation analysys of Gorlin syndrome
Study
JGAS000099
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Japanese Reference Genome JG1
Study
JGAS000259
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C-MACH reduced-representation bisulfite sequencing (RRBS)
Study
JGAS000171
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Development of the prevention and therapy of CRC using patient derived culture tissues.
Study
JGAS000139
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Whole-exome sequencing of pediatric solid tumors
Study
JGAS000036
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Development of a diagnostic gene panel for Gorlin syndrome and its application to liquid biopsy
Study
JGAS000308
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Whole genome, whole exome and transcriptome sequencing of 10 ccRCC with Von Hippel-Lindau disease
Study
JGAS000544
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Identification of responsible genes and development of standardized medicine for familial breast cancer by genetic analysis with NGS technology
Study
JGAS000224
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Demographic History and Local Adaptation in Asian Population
Study
JGAS000238