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Philippine Ayta possess the highest level of Denisovan ancestry in the world
Study
EGAS00001005407
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Philippine Ayta possess the highest level of Denisovan ancestry in the world
Study
EGAS00001005408
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Whole genome sequencing (bam files) of 5 samples of myxofibrosarcoma and 5 matched pairs
Study
EGAS00001005444
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Genetics causes of male infertility in 185 patient-parent trios from Netherlands and UK
Study
EGAS00001005417
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Feasibility of Ultra-Rapid Exome Sequencing in Critically Ill Infants and Children With Suspected Monogenic Conditions in the Australian Public Health Care System
Study
EGAS00001005430
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Spatial concordance of DNA methylation classification in diffuse glioma
Study
EGAS00001005434
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Whole exome sequencing (bam files) of 55 samples of myxofibrosarcoma and 44 matched pairs
Study
EGAS00001005442
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Targeted-capture sequencing (bam files) of 81 samples of myxofibrosarcoma and 44 matched pairs
Study
EGAS00001005443
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Next Generation Sequencing platform for targeted Personalized Therapy of Leukemia - Acute myeloid leukemia
Study
EGAS00001005464
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The PEMDAC phase 2 study of pembrolizumab and entinostat in patients with metastatic uveal melanoma
Study
EGAS00001005478
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An epigenomics time course analysis of covid19 patients from Quebec, Canada
Study
EGAS00001005468
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Epigenetic encoding, heritability and plasticity of glioma transcriptional cell states
Study
EGAS00001005472
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Role of cohesin/CTCF in human monocyte differentiation
Study
EGAS00001005508
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Methylation clocks - individual colon, small intestine and endometrial crypts
Study
EGAS00001005514
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Multi-omics integration reveals only minor long-term molecular and functional sequelae in immune cells of individuals recovered from COVID-19
Study
EGAS00001005529
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Pancreatic islets PISA RNA-seq samples
Study
EGAS00001005535
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Investigation of the keratinocytic gene expression pattern in Hidradenitis suppurativa
Study
EGAS00001005544
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Genomic characterization of retinoblastoma (targeted sequencing)
Study
EGAS00001005550
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Pediatric study using genome sequencing
Study
EGAS00001005553
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DLBCL NGS Genomic Datasets of non-China cohort from Phoenix Clinical Trial
Study
EGAS00001005554
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Mitochondrial DNA sequencing of iPSC, parental cells, and iPSC derived cardiomyocytes
Study
EGAS00001005560
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Whole genome sequencing of a breast cancer cohort with known functional homologous recombination status
Study
EGAS00001005572
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Genetics and therapeutic responses to TIL therapy of pancreatic cancer PDX models
Study
EGAS00001005596
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IVF Whole genome prediction
Study
EGAS00001005619
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Small variants in mtDNA Canary Islands - WES Illumina (ITER)
Study
EGAS00001005678
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SudanMitoSeq: Sudanese mitochondrial sequencing
Study
EGAS00001005669
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Germline biallelic mutation affecting the transcription factor Helios causes pleiotropic defects of immunity
Study
EGAS00001005675
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Small variants in mtDNA Canary Islands - WGS Oxford Nanopore Technologies (ITER)
Study
EGAS00001005677
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Small variants in mtDNA Canary Islands - WGS Illumina (ITER)
Study
EGAS00001005679
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Pediatric HGG WES and RNA-Seq
Study
EGAS00001005687
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Human genomic and phenotypic synthetic data for the study of rare diseases
Study
EGAS00001005702
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Genetic variability in exon 1 of the glucocorticoid receptor gene NR3C1 is associated with postoperative complications
Study
EGAS00001005737
-
Proteogenomics of chronic lymphocytic leukemia
Study
EGAS00001005746
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Genome-wide Rare Variant Score Associates With Morphological Subtypes of Autism Spectrum Disorder
Study
EGAS00001005753
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Searching for genetic modulators of the phenotypic heterogeneity in Brugada Syndrome
Study
EGAS00001005848
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Identification of Germline Monoallelic Mutations in IKZF2 in Patients with Immune Dysregulation.
Study
EGAS00001005874
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Genome-wide genotype data for 1,433 ni-Vanuatu
Study
EGAS00001005910
-
Combination therapies to inhibit LCK tyrosine kinase and mTOR signaling in T-cell Acute Lymphoblastic Leukemia
Study
EGAS00001005945
-
The Proteogenomic Subtypes of Acute Myeloid Leukemia
Study
EGAS00001005950
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An Isogenic Cell Line Panel for Sequence-based Screening of Targeted Anti-cancer Drugs
Study
EGAS00001005974
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Germline TP53 mutations undergo copy number gain years prior to tumor diagnosis
Study
EGAS00001005982
-
Host genotyping data from Dutch adult bacterial meningitis patients and linked bacterial genome sequences
Study
EGAS00001005993
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Multimodal immunogenomic biomarker analysis of tumors from pediatric patients enrolled to a phase 1-2 study of single-agent atezolizumab
Study
EGAS00001006004
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Human genome-wide variations in the Massim region
Study
EGAS00001006010
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Drug-induced epigenomic plasticity reprograms circadian rhythm regulation to drive prostate cancer towards androgen-independence (RNA-seq)
Study
EGAS00001006016
-
Drug-induced epigenomic plasticity reprograms circadian rhythm regulation to drive prostate cancer towards androgen-independence (ChIP-seq)
Study
EGAS00001006017
-
Papuan Y chromosome Diversity Panel
Study
EGAS00001006025
-
CIRdb: Array genotype data
Study
EGAS00001006050
-
Insights from genome-wide data from Thailand and Laos
Study
EGAS00001006053
-
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants
Study
EGAS00001006058