-
Genetic insights into the biological mechanisms governing human ovarian ageing
Study
EGAS00001004947
-
Comparison of the diagnostic yield of aCGH and NGS across different neurodevelopmental disorders
Study
EGAS00001004949
-
Cell-free DNA TAPS for early cancer detection
Study
EGAS00001004962
-
Genetic heterogeneity and dynamics of transcriptional subtypes in matched primary and recurrent head and neck squamous cell carcinomas
Study
EGAS00001005005
-
DO NOT USE - Whole genome sequencing of SI-NETs from six patients
Study
EGAS00001005009
-
Deep genetic affinity between coastal Pacific and Amazonian natives evidenced by Australasian ancestry
Study
EGAS00001005022
-
Genetic analysis of HLA and immune escape genes in Diffuse Large B-cell Lymphoma
Study
EGAS00001005054
-
Multiple migrations to the Philippines during the last 50,000 years
Study
EGAS00001005083
-
Mutational analysis of an oligoprogressive sarcomatoid hepatocellular carcinoma treated with an immune checkpoint inhibitor.
Study
EGAS00001005064
-
Genetic landscape of inherited retinal dystrophies affected cases in Spain
Study
EGAS00001005104
-
Chronic myelomonocytic leukemia
Study
EGAS00001005107
-
Sequencing of cancer autopsies and ctDNA
Study
EGAS00001005109
-
International Genetics of Parkinson Disease Progression (IGPP) Consortium GWAS Summary Results
Study
EGAS00001005110
-
mRNA capture sequencing and RT-qPCR for the detection of pathognomonic, novel and secondary fusion transcripts in formalin-fixed paraffin-embedded tissue: a sarcoma showcase
Study
EGAS00001005202
-
Radiation-induced gliomas represent H3-/IDH-wild type pediatric gliomas with recurrent PDGFRA amplification and loss of CDKN2A/B
Study
EGAS00001005243
-
Novel optineurin frameshift insertion causing familial frontotemporal dementia and parkinsonism without amyotrophic lateral sclerosis
Study
EGAS00001005220
-
Targeted sequencing of follicular lymphoma tumour samples from the UK's Haematological Malignancy Research Network
Study
EGAS00001005238
-
Mutational bias in spermatogonia impacts the anatomy of regulatory sites in the human genome
Study
EGAS00001005366
-
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
-
SG Peranakan Project: Genetic admixture in the culturally unique Peranakan Chinese population in Southeast Asia
Study
EGAS00001005379
-
Interferon lambda 4 impairs viral antigen presentation and attenuates T cell responses
Study
EGAS00001005396
-
Genomic characterization of co-existing biliary tract intraepithelial neoplasia and carcinoma lesions reveals distinct evolutionary paths of gallbladder cancer
Study
EGAS00001005402
-
Germline RUNX1 Variation and Predisposition to Childhood Acute Lymphoblastic
Study
EGAS00001005403
-
Philippine Ayta possess the highest level of Denisovan ancestry in the world
Study
EGAS00001005407
-
Philippine Ayta possess the highest level of Denisovan ancestry in the world
Study
EGAS00001005408
-
Whole genome sequencing (bam files) of 5 samples of myxofibrosarcoma and 5 matched pairs
Study
EGAS00001005444
-
Whole exome sequencing (bam files) of 55 samples of myxofibrosarcoma and 44 matched pairs
Study
EGAS00001005442
-
Targeted-capture sequencing (bam files) of 81 samples of myxofibrosarcoma and 44 matched pairs
Study
EGAS00001005443
-
An epigenomics time course analysis of covid19 patients from Quebec, Canada
Study
EGAS00001005468
-
Mitochondrial DNA sequencing of iPSC, parental cells, and iPSC derived cardiomyocytes
Study
EGAS00001005560
-
Role of cohesin/CTCF in human monocyte differentiation
Study
EGAS00001005508
-
Investigation of the keratinocytic gene expression pattern in Hidradenitis suppurativa
Study
EGAS00001005544
-
Genomic characterization of retinoblastoma (targeted sequencing)
Study
EGAS00001005550
-
Pediatric study using genome sequencing
Study
EGAS00001005553
-
DLBCL NGS Genomic Datasets of non-China cohort from Phoenix Clinical Trial
Study
EGAS00001005554
-
Whole genome sequencing of a breast cancer cohort with known functional homologous recombination status
Study
EGAS00001005572
-
IVF Whole genome prediction
Study
EGAS00001005619
-
Small variants in mtDNA Canary Islands - WES Illumina (ITER)
Study
EGAS00001005678
-
Germline biallelic mutation affecting the transcription factor Helios causes pleiotropic defects of immunity
Study
EGAS00001005675
-
Small variants in mtDNA Canary Islands - WGS Oxford Nanopore Technologies (ITER)
Study
EGAS00001005677
-
Small variants in mtDNA Canary Islands - WGS Illumina (ITER)
Study
EGAS00001005679
-
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
-
Genome-wide Rare Variant Score Associates With Morphological Subtypes of Autism Spectrum Disorder
Study
EGAS00001005753
-
Searching for genetic modulators of the phenotypic heterogeneity in Brugada Syndrome
Study
EGAS00001005848
-
Identification of Germline Monoallelic Mutations in IKZF2 in Patients with Immune Dysregulation.
Study
EGAS00001005874
-
Genome-wide genotype data for 1,433 ni-Vanuatu
Study
EGAS00001005910
-
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
-
Multimodal immunogenomic biomarker analysis of tumors from pediatric patients enrolled to a phase 1-2 study of single-agent atezolizumab
Study
EGAS00001006004