14501 results for "PLOS+ONE+Pennsylvania+German+ACS+language+code+pdc+open+access+study"

in 14.58 milliseconds.

• Mutational consequences of hematopoietic stem cell transplantation in humans

  Study EGAS00001004926

• Whole Exome sequencing data from Shwachman-Diamond syndrome bone marrow samples

  Study EGAS00001004880

• Sensitive and reproducible cell-free methylome quantification with synthetic spike-in controls

  Study EGAS00001005069

• Epigenetic encoding, heritability and plasticity of glioma transcriptional cell states

  Study EGAS00001005472

• Initial cohort of 500 solid tumors screened for Basket of Baskets

  Study EGAS00001005893

• Obesity and hyperinsulinemia drive adipocytes to activate a cell cycle program and senesce

  Study EGAS00001005770

• Searching for genetic modulators of the phenotypic heterogeneity in Brugada Syndrome

  Study EGAS00001005848

• Targeted de novo phasing and long-range assembly by template mutagenesis

  Study EGAS00001005899

• Genomic insights into the population history of the Resande or Swedish Travellers

  Study EGAS00001006176

• Whole Exome and RNA sequencing of synchronous female bilateral breast cancers

  Study EGAS00001006910

• Whole genome, RNA-seq and single-cell Multiome profile of multiple myeloma

  Study EGAS00001007014

• Cell-to-cell variability in Myc dynamics drives transcriptional heterogeneity in cancer cells

  Study EGAS00001007091

• Genomic Landscape of Follicular Lymphoma Across a Wide Spectrum of Clinical Behaviors

  Study EGAS00001007105

• CITE-seq for peripheral blood samples of 5 breast cancer patients

  Study EGAS00001006241

• Multi-omics analysis of an individual with multiple pancreatic neuroendocrine tumours (panNETs)

  Study EGAS00001006722

• Validation study of genome-wide polygenic score for body mass index in South Asians

  Dac EGAC00001003593

• RNA sequencing of chondrosarcoma

  To profile chondrosarcoma patients.

  Study EGAS00001004585

• CGP_CORE_CELL_LINES___RNA_seq

  Graham to complete

  Study EGAS00001000828

• IBD_Whole_Genome_Sequencing_Phase_1

  IBD Whole Genome Sequencing Phase 1

  Study EGAS00001001735

• Exome sequencing

  Exome sequence Pfizer & TwinsUK

  Study EGAS00001001194

• Stabilising selection causes grossly altered but stable karyotypes in metastatic colorectal cancer

  Study EGAS00001004219

• Acne meta-analysis

  Acne meta-analysis

  Dataset EGAD00001008342

• Effects of interferon-gamma treatment on human small intestinal organoids generated from healthy donors

  The intestine is vulnerable to interferon-gamma as intestinal epithelial stem cells undergo cell death when exposed to interferon-gamma. Here, we developed a novel human intestinal organoid-based 3D model system to study the effects of interferon-gamma-induced intestinal epithelial damage at the RNA level. We treated organoids with 10 ng/mL for either 6 or 18h. Knowledge generated with this dataset is relevant for a variaty of intestinal pathologies with an immune component, for instance graft-versus-host disease.

  Study EGAS50000000083

• VariantMedium: Sensitive and generalizable somatic point mutation calling with 3D DenseNets trained and evaluated on experimental confirmation data

  This study contains whole-exome sequencing (WES) and results of targeted deep-sequencing data of five matched tumor and normal cell lines, with two technical WES replicates each. The calls by Mutect2, Strelka2, and VariantMedium were confirmed using targeted deep sequencing on Illumina Miseq The targeted deep sequencing was performed in three runs and the results are summarized under VCF files, with labels determined for 1663 point mutations and 201 insertion-deletions.

  Study EGAS00001007633

• Whole Exome Sequencing for Colorectal Cancer

  This project was designed to use next generation sequencing technology to screen the protein coding regions of the genome for low frequency variants in a panel of high-risk colorectal adenocarcinoma cases. Blood and cell-line DNA for colorectal cancer patients and a subset of quality control samples that had existing whole exome sequence data were analyzed using Illumina HiSeq sequencers. Samples from this project were from participants in the Women's Health Initiative (WHI) and the Diet, Activity, and Lifestyle Study (DALS).

  Study phs000410