14450 results for ""Pennsylvania+German"+ACS+study+'Socius'+open+access"

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• H3Africa - Genomic Characterization and Surveillance of Microbial Threats in West Africa

  Viral diseases are remarkably heterogeneous in their presentation and clinical course. Although diseases such as Lassa Fever and Ebola Virus Disease are thought to be severe and rapidly fatal, they can often present with mild symptoms or remain asymptomatic. Host genetic variability is likely an important mediator of this heterogeneity. Complete characterization of the clinical, laboratory, and host genetic features of these illnesses is not only imperative to rapid diagnosis and effective clinical care, but also important for further scientific study. In this project, we propose to address this need through deep characterization of the clinical and laboratory features of viral disease and through study of genetic mediators of resistance to Lassa Fever and Ebola Virus Disease. Will carry out deep clinical characterization and laboratory assessment of viral febrile cases at two West African Collaborative Centers, and will use this data to develop prognostic models using cutting-edge tools in exploratory data visualization and machine learning. Investigate host genetic factors of Lassa Fever and Ebola Virus Disease through genome-wide association studies. We will then develop field-deployable genotyping assays for the top-associated variants, and apply them in new cohorts to replicate our findings and investigate patterns of genetic resistance in clinical subgroups. This project can shed light on the clinical manifestations of viral illness and their host genetic mediators, leading to potential new insights in disease biology and pathophysiology. We will also create a rich resource of clinical, laboratory, and genetic data for these illnesses in two countries in West Africa, which will serve as a foundation for advancing the clinical care and scientific study of viral disease in the region.

  Study EGAS00001007250

• CPCG-200PG-ARRAY

  Raw Array data from the CPCGene 200PG study

  Dataset EGAD00010001218

• Proteom study primary CRC and LM

  Proteom characterization in primary colorectal cancer and corresponding liver metastasis

  Dataset EGAD00010002237

• Single-Cell RNA-seq of Primary High Grade Serous Carcinoma

  Single-cell RNA Sequencing of CD45- cancer cells.

  Study EGAS50000000068

• TRACERx NSCLC - Whole exome multiregion sequencing data

  Study EGAS00001006494

• Dnase1l3 knockout causes aberrations in plasma DNA fragmentation

  Dnase1l3 knockout causes aberrations in plasma DNA fragmentation

  Study EGAS00001003174

• HCA_Skin_Disease_WSSS_Spatial_NCL

  Defining the spatial transcriptome and cell-cell interactions in eczema and psoriasis skin

  Study EGAS00001005278

• Brain_Disease_Wellcome_Leap_Delta_Tissue_Spatial

  Utilising Spatial Transcriptomics to investigate how the tumour microenvironment regulates glioblastoma cell states.

  Study EGAS00001005801

• Gene_Discovery_in_Age_Related_Hearing_Loss

  The aim is to find new candidate genes associated with progressive hearing loss

  Study EGAS00001000295

• Whole genome and transcriptome analysis of anaplastic thyroid carcinoma

  Whole genome and transcriptome analysis of anaplastic thyroid carcinoma

  Study EGAS00001001214

• ORCADES_15x

  15x whole genome sequencing in samples from the isolated population of Orkney

  Study EGAS00001001891

• Identifying_new_diagnostic_and_treatment_pathways_for_patients_with_unclassifiable_sarcomas

  Whole genome sequencing of tumour normal pairs of human undifferentiated sarcomas.

  Study EGAS00001001604

• SSBP1

  SSBP1 mutations cause a complex optic atrophy spectrum disorder with mitochondrial DNA depletion

  Study EGAS00001004003

• GIST_SSGXVIII_trial_targeted_gene_sequencing

  Targeted cancer gene sequencing of samples enrolled in the SSGXVIII trial from Finland.

  Study EGAS00001001054

• The_genetic_evolution_of_precursor_lesions_in_pancreatic_cancer

  Mapping genetic evolution of pancreatic cancer precursor lesions such as IPMNs and PanINs.

  Study EGAS00001001573

• BLUEPRINT EpiVar ChIP-seq of Monocytes & Neutrophils

  BLUEPRINT EpiVar ChIP-seq of Monocytes & Neutrophils

  Study EGAS00001000870

• IACS treatment on breast cancer bone metastases

  Off-target effect of IACS on breast cancer bone metastases.

  Study EGAS00001006908

• HSP90 inhibitor resistant cell line

  Genetic analysis of K562 cell which are resistant against HSP90 inhibitors.

  Study EGAS00001006381

• Reference epigenome ADMSC06 WGBS data generated from KEP study

  ADMSC06 WGBS paired end data

  Dataset EGAD00001007137

• Reference epigenome ADMSC08 WGBS data generated from KEP study

  ADMSC08 WGBS paired end data

  Dataset EGAD00001007139

• Reference epigenome IPS-NPC02 h3k4me3 ChIP-Seq data generated from KEP study

  IPS-NPC02 h3k4me3 ChIP-Seq paired end data

  Dataset EGAD00001007288

• Reference epigenome ADMSC05 WGBS data generated from KEP study

  ADMSC05 WGBS paired end data

  Dataset EGAD00001007136

• Reference epigenome ADMSC07 WGBS data generated from KEP study

  ADMSC07 WGBS paired end data

  Dataset EGAD00001007138

• Reference epigenome IPS01_N_Fibroblast_WGBS data generated from KEP study

  A IPS01_N_Fibroblast_WGBS paired end data for iPSC(Oct4)

  Dataset EGAD00001003473

• Reference epigenome IPS04_X_Fibroblast_WGBS data generated from KEP study

  A IPS04_X_Fibroblast_WGBS paired end data for iPSC(Oct4)

  Dataset EGAD00001003476