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Characterizing microbiome-directed fibre snacks in gnotobiotic mice and humans
Study
EGAS00001005268
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Molecular characteristics in Burkitt lymphoma over age groups
Study
EGAS00001005270
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Whole genome, whole exome, and targeted sequencing of high-grade meningioma tumor samples.
Study
EGAS00001002294
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Exome_trios_in_patients_with_gastroschisis
Study
EGAS00001002664
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Clonal_haematopoiesis_in_patients_with_AAA
Study
EGAS00001002873
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IDENTIFICATION AND TARGETED MANAGEMENT OF A PATIENT WITH A NEURODEGENERATIVE DISORDER CAUSED BY BIALLELIC MUTATIONS IN SLC5A6
Study
EGAS00001003861
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Rapid identification of somatic genome rearrangements as personalized biomarkers for blood-based cancer monitoring
Study
EGAS00001003963
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Mutational Patterns in Metastatic Cutaneous Squamous Cell Carcinoma
Study
EGAS00001003370
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Native American gene flow into Polynesia predating Easter Island settlement
Study
EGAS00001004209
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Reconstituting the transcriptome and DNA methylome landscapes of human implantation at single-cell resolution
Study
EGAS00001003443
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Molecular determinants of response to PD-L1 blockade across tumor types
Study
EGAS00001004343
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Large-scale viral genome analysis identifies novel clinical associations between hepatitis B virus and chronically infected patients
Study
EGAS00001003689
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A system-wide approach to monitor responses to synergistic BRAF and EGFR inhibition in colorectal cancer cells
Study
EGAS00001002654
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The_Genomic_Advances_in_Sepsis__GAinS__RNA_seq
Study
EGAS00001003772
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Extreme phenotypes define epigenetic and metabolic signatures in cardiovascular diseases.
Study
EGAS00001003780
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Single cell phenotypic profiling of 27 DLBCL cases reveals marked inter- and intra-tumoral heterogeneity
Study
EGAS00001003860
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Bisulfite-converted duplexes for the strand-specific detection and quantification of rare mutations
Study
EGAS00001002406
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Biallelic mutations in the ubiquitin ligase RFWD3 cause Fanconi anemia
Study
EGAS00001002440
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Genome-wide DNA Methylation is Predictive of Outcome in Juvenile Myelomonocytic Leukemia
Study
EGAS00001002700
-
Hermansky-Pudlak syndrome type 1 causes impaired anti-microbial immunity through a pathogenic lipid metabolism-mTOR circuit
Study
EGAS00001005053
-
THE GENOMIC LANDSCAPE OF ACTINIC KERATOSIS
Study
EGAS00001004243
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Interplay of somatic alterations and immune infiltration modulates response to PD-1 blockade in advanced clear cell RCC -- CA209-010
Study
EGAS00001004291
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This project aims to study human memory capacity, including short-term memory and long-term memory, systematically via genome-wide association studies
Study
EGAS00001002875
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A Protein Neddylation Inhibitor MLN4924 Suppresses Patient-Derived Glioblastoma Cells via Inhibition of ERK and AKT Signaling
Study
EGAS00001004018
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Hypoxia acts as an environmental cue for the human TRM differentiation program
Study
EGAS00001005286
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To determine the mutational impact of the in vitro culture, clonal human adult and pluripotent stem cell lines were subjected to a second clonal step after 3 months of culture. These subclones were whole genome sequenced to identify all the mutations that accumulated during the 3 month culture period.
Study
EGAS00001002955
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The Molecular Landscape of Asian Breast Cancers Reveals Clinically Relevant Population-Specific Differences
Study
EGAS00001004518
-
Host whole genome variations are associated with neurocognitive outcome in survivors of pediatric medulloblastoma
Study
EGAS00001002996
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Whole genome, exome and transcriptome analysis to guide individualized cancer interpretation
Study
EGAS00001004013
-
Hermansky-Pudlak syndrome type 1 causes impaired anti-microbial immunity through a pathogenic lipid metabolism-mTOR circuit - 10x Genomics scRNAseq
Study
EGAS00001005098
-
Variation and transmission of the human gut microbiota across generations - shotgun data
Study
EGAS00001005649
-
Variation and transmission of the human gut microbiota across generations - 16S data
Study
EGAS00001005651
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Nanopore_and_Illumina_sequencing_of_human_glioblastomas
Study
EGAS00001005812
-
A recessive PRDM13 mutation results in congenital hypogonadotropic hypogonadism and cerebellar hypoplasia
Study
EGAS00001005878