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Mutational Spectrums and Clinical Features of Patients with LOXHD1 Variants Identified in a 8,074 Hearing Loss Patient Cohort.
Study
JGAS000192
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snRNA and snATAC analysis of cocaine use disorder in human caudate nucleus
Study
EGAS50000000480
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Personalized analysis of ctDNA for detection of molecular residual disease and recurrence in a cohort of surgically treated patients with head and neck squamous cell carcinoma
Study
EGAS50000001018
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Multifocal cohort analysis unveils cell types associated with regional lymph node seeding in prostate cancer
Study
EGAS00001006715
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H3K27ac ChIP-seq in primary inflammatory (TPP) macrophages
Study
EGAS00001007562
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Investigating genetic susceptibility to rheumatic heart disease in Oceania
Study
EGAS00001001881
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TERT rearrangements are frequent in neuroblastoma and identify aggressive tumors
Study
EGAS00001001479
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A Comparative Analysis of Algorithms for Somatic SNV Detection in Cancer
Study
EGAS00001000927
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Genetic ancestry contributes to somatic mutations in lung cancers from admixed Latin American populations
Study
EGAS00001004752
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Whole genome sequencing of primary and metastatic Melanoma cases in an Australian cohort.
Study
EGAS00001001552