14670 results for "PLOS+ONE+Pennsylvania+German+ACS+language+code+pdc+open+access+study"

in 14.13 milliseconds.

• EORTC study on the evolution of driver mutations and MGMT promotor methylation in glioblastomas treated with standard of care: Correlation with survival and impact on trial design

  Precision medicine trials in glioblastoma should be conducted at tumor recurrence. However, second surgery for recurrent GBMs is not routinely performed and therefore molecular data is predominantly derived from primary samples. This study aims to establish the frequency of driver changes at tumor recurrence.

  Dataset EGAD00001004593

• GoDARTS T2D-GENES Exome Sequencing Study

  The GoDARTS T2D-GENES exome sequencing study includes 1924 samples, 965 T2D cases and 959 T2D controls, from European ancestry. This cohort is part of a larger exome sequencing effort from the T2D-GENES project and contains the exome sequencing vcf from the GoDARTS samples. The other data generated from the T2D-GENES project can be found in dbGAP. Samples underwent deep exome sequencing, with SNVs and INDEls called according to GATK best practices.

  Dataset EGAD00001004311

• Gene_epression_regulation_in_cytokine_induced_immune_cell_states

  We isolated T cells and monocotyes from healthy platelet donors and cultured them in resting and stimulated conditions with addition of a range of cytokines. We performed RNA sequencing to assess impact of different disease-relevant cytokines upon immune cell responses.

  Study EGAS00001003823

• Study of Korean Parkinson's disease

  Single nucleotide variants (SNVs) associated with Parkinson’s disease (PD) have been investigated mainly through genome-wide association studies. Here, we conducted whole genome sequencing of 410 PD patients and 200 healthy individuals of the Korean population and identified disease-related SNVs.

  Study EGAS00001006811

• Reconstruction of human terminal erythroid differentiation cell at single cell level

  Study EGAS00001003114

• Quantitative analysis of a novel DNA hypermethylation panel for lung cancer diagnosis

  Study EGAS00001007008

• DAC for study Screening for abnormal CGI methylation in primary colorectal tumours

  Dac EGAC00001000069

• MeDIP-seq data in the Peri/postnatal Epigenetics Twins Study (PETS)

  Dac EGAC00001000596

• The APL DAC comprises a clinician and biologist who conducted the study.

  Dac EGAC00001000865

• DAC for the study of tumor-derived somatic mutation detection in cfDNA

  Dac EGAC00001001569

• Finland Myoma Study

  Dac EGAC00001002131

• EXCEED Study genotypes

  EXCEED genotyping

  Dataset EGAD00010001699

• Rapid, economical diagnostic classification of ATRT molecular subgroup using NanoString nCounter platform

  Study EGAS00001007470

• Gene expression profiling of HGCC patient-derived Glioblastoma Cell Lines (ISPA-GBM)

  Study EGAS00001006814

• Targeted sequencing of 13131 older individuals, using 750-gene panel

  Study EGAS00001005316

• The effects of inhaled corticosteroids on healthy airways

  Study EGAS00001007538

• Panic study

  To manage Panic saliva microbiota 16S data produced in collaboration.

  Dac EGAC50000000408

• Whole genome sequencing of matched primary and metastatic acral melanomas

  Study EGAS00001000169

• A Comprehensive Catalogue of Somatic Mutations from a Human Cancer Genome

  Study EGAS00001000245

• Diagnostic Exome Sequencing in Persons with Severe Intellectual Disability

  Study EGAS00001000287

• Whole exome sequencing of virus-associated HCC

  Study EGAS00001000389

• Mitochondrial DNA (mtDNA) analyses in patients with schizophrenia and healthy control individuals

  Study EGAS00001003269

• Mechanisms of active DNA demethylation in human monocytes

  Study EGAS00001004784

• ATAC-Seq and CTCF ChIP-Seq on the OCIAML-2 cell line

  Study EGAS00001004741

• Characterization of human iPSC-derived dopaminergic neurons with 16p11.2 CNVs

  Study EGAS00001005137