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Precision Diagnosis of Neurodevelopmental Disorders in Middle Eastern Populations
Study
phs003917
-
Identification of novel fusion genes in lung cancer using breakpoint assembly of transcriptome sequencing data
Study
EGAS00001000659
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Targeted de novo phasing and long-range assembly by template mutagenesis
Dataset
EGAD00001008444
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NHLBI TOPMed: Walk-PHaSST Sickle Cell Disease (SCD)
Study
phs001514
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SEER Remote Access Pilot Test Data (2018)
Study
phs002012
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1000 Genomes Used for Cloud Testing
Study
phs000710
-
ucfDNA workflows for molecular profiling of malignant disease
Study
EGAS50000001093
-
Tracking the origins and drivers of subclonal metastatic expansion in prostate cancer
Study
EGAS00001000942
-
Rna-Seq Leiomyosarcoma subtypes
Study
EGAS00001004783
-
Latency and interval therapy affect the evolution in metastatic colorectal cancer
Study
EGAS00001003646
-
WES analysis of DMD-ASD, DMD-ID and DMD-Control individuals for de novo and rare risk variants analysis
Dataset
EGAD50000001113
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Targeted sequencing data of regulatory regions in 200 Spanish ASD trios
Dac
EGAC50000000695
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Merged analysis-ready bam files: HiSeq sequencing of matched tumour/normal DNA samples from Pancreatic Ductal Adenocarcinoma cases
Dataset
EGAD00001002192
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Chromatin accessibility analysis of hepatocyte-like cell in vitro differentiation from iPSC in comparison to primary human hepatocytes
Dataset
EGAD00001005934
-
mRNA-seq of in vitro differentiation from induced pluripotent stem cells to hepatocyte-like cells
Dataset
EGAD00001005935
-
BRCA1 secondary splice-site mutations
Study
EGAS50000000022
-
Luminal progenitor cell line iHBEC(CD117)
Dataset
EGAD50000000723
-
The Role of Germline Mutation and Parental Age in Autism Spectrum Disorders
Study
phs001164
-
Impact of Genetic Variation on Response to GO Therapy in COG-AML Trials AAML03P1 and AAML0531
Study
phs003490
-
Molecular Genetic Studies of Developmental Brain Disorders
Study
phs000455
-
NHLBI TOPMed - NHGRI CCDG: The Vanderbilt University BioVU Atrial Fibrillation Genetics Study
Study
phs001624
-
Team
Documentation
about/team
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Pervasive H3K27 acetylation and ERV expression in H3.3K27M gliomas present a therapeutic vulnerability
Study
EGAS00001003572
-
16 Year Life History and Genomic Evolution of an ER+ HER2- Breast Cancer
Study
EGAS00001004624
-
Whole transcriptome RNA sequencing on bone marrow and peripheral blood samples from patients with acute myeloid leukemia at diagnosis or relapse.
Dataset
EGAD00001004187