14504 results for "PLOS+ONE+Pennsylvania+German+ACS+language+code+pdc+open+access+study"

in 14.88 milliseconds.

• Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features

  Study EGAS00001005346

• Somatic mutations in healthy and leukemic blood progenitors reveal evolutionary mechanisms underlying childhood leukemia and differential patient outcome

  Study EGAS00001004593

• Gene expression profiles of disseminated breast cancer cells

  Study EGAS00001004597

• Nanopore sequencing from liquid biopsy: analysis of copy number variations from cell-free DNA of lung cancer patients

  Study EGAS00001004975

• Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features

  Study EGAS00001005355

• RNA-seq on neuroblastoma PDX model COG-N-519 treated with control miR-1283 and test miR-99b-5p mimics

  Study EGAS00001005368

• Whole transcriptome profiling of liquid biopsies from tumour xenografted mouse models enables specific monitoring of tumour-derived extracellular RNA

  Study EGAS00001005740

• Single-cell multi-omics of human clonal hematopoiesis reveals that DNMT3A R882 mutations perturb early progenitor states through selective hypomethylation.

  Study EGAS00001006364

• transcriptome analysis of NK cells sorted from PBMCs at baseline and after addition of a T cell dependent bispecific antibody (TDB)

  Study EGAS00001006914

• The effector program of human CD8 T cells can promote both target cell killing and tissue remodeling

  Study EGAS00001006960

• RNA sequencing of in vitro generated suppressive myeloid cells using parental and Sialidase expressing A549 cancer cell lines

  Study EGAS00001007618

• DAC for study involving the spatial transcriptomics analysis of HPV-dependent and HPV-independent vulval squamous cell carcinoma at Imperial College London.

  Dac EGAC00001003515

• Structural and Non-Coding Variants Increase the Diagnostic Yield of Clinical Whole Genome Sequencing for Rare Diseases

  Study EGAS00001007575

• A single cell view on host immune transcriptional response to in vivo BCG-induced trained immunity

  Study EGAS00001006990

• Genomic and immune signatures predict clinical outcome in newly diagnosed multiple myeloma treated with immunotherapy regimens

  Study EGAS00001007404

• Precise reconstruction of the tumor microenvironment using bulk RNA-seq and a unique machine learning-based algorithm trained on artificial transcriptomes

  Study EGAS00001006272

• Targeted gene panel sequencing of leiomyosarcoma

  We conducted MSK-IMPACT sequencing of leiomyosarcoma.

  Study EGAS50000000595

• LICA-CN project - 116 liver cancer cases

  LICA-CN project - 116 liver cancer cases

  Study EGAS00001002300

• Whole_exome_sequencing_of_inflammatory_bowel_disease_cases

  Whole exome sequencing of around 700 inflammatory bowel disease cases.

  Study EGAS00001000530

• Integrative Molecular Classification of Meningiomas

  Integrative Molecular Classification of Meningiomas

  Study EGAS00001004982

• ChIP-Seq of TFEB in LT-HSC

  ChIP-Seq of TFEB in LT-HSC

  Study EGAS00001005462

• Cell-free DNA cleavages analysis (human)

  Cell-free DNA cleavages analysis (human)

  Study EGAS00001006701

• Complete Genomics dataset for study EGAS00001002275.

  TBD

  Dataset EGAD00001003187

• Datasets 929/938

  Datasets Galaxy 929/938 describe the amplified single chromosome sequencing data.

  Dataset EGAD00001004457

• Single cell RNA sequencing reveals induced bifurcated differentiation after RUNX1::RUNX1T1 depletion in patient-derived leukemic blasts

  Study EGAS00001008050