19219 results for "Buy fc coins Buyfc26coins.com is EA Sports official for FC 26 coins They are the best FC seller..nEoY"

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• Mutational landscape of renal cell carcinoma with venous tumor thrombus

  Renal cell carcinoma with venous tumor thrombus opens the unique opportunity to investigate the clonal evolution of a tumor in two fundamentally different compartments i.e., within the confinement of an organ and inside a large blood vessel. We performed multiregion whole exome sequencing of a total of 37 samples from five consecutive patients (normal tissue, n=5; primary tumors, n=16; tumor thrombi, n=16) to >35-fold target coverage. Four patients had a clear cell RCC, one patient had a poorly differentiated type II papillary RCC (RCC-VTT-04). The latter patient had a friable thrombus, the others were of solid consistency.

  Study EGAS00001001950

• The Genetic Analysis of multiple sclerosis

  We created these data in order to identify genetic variants associated with increased susceptibility to multiple sclerosis. Cases from many parts of the world were genotyped with the Illumina 660 chip along with Swedish controls. In our analysis we also used control data from the WTCCC2 common UK controls and from other published studies.

  Study EGAS00000000101

• Molecular Features of Hepatocellular Carcinoma Associated with 18F-Fluorocholine PET/CT Imaging Phenotype

  Molecular imaging with 18F-fluorocholine PET/CT reveals two distinct imaging phenotypes for hepatocellular carcinoma (HCC) as a potential source of non-invasive insight into its molecular heterogeneity. Using gene set enrichment analyses, we found 18F-fluorocholine-avid tumors to be significantly enriched by genes comprising a subset of previously published HCC-related gene signatures. Significant gene sets included those from existing molecular classification systems for HCC as well as gene signatures predictive of clinical outcomes after tumor resection. PET/CT imaging using 18F-fluorocholine might therefore provide surrogate information about tumor molecular characteristics and prognosis in HCC.

  Study phs001784

• Bulk RNA-seq of monocytes and in vitro cultured monocyte-derived macrophages of ANCA-associated vasculitis patients with active and stable disease and healthy controls

  To study monocyte and macrophage activation in ANCA-associtated vasculitis (AAV), we performed bulk RNA sequencing of bead-selected monocytes and in vitro cultured monocyte-derived macrophages from AAV patients and healthy controls. Overview patients included for sequencing monocytes: - AAV active disease, n=4, MPO-AAV=4 - AAV remission, n=10, PR3-AAV=5, MPO-AAV=5 - Healthy controls, n=6 Overview patients included for sequencing monocyte-derived macrophages: - AAV active, n=1, PR3-AAV=1 - AAV remission, n=3, PR3-AAV=3 - Healthy controls, n=3

  Study EGAS50000000311

• NanoSring of PBMC from bladder cancer and RCC patients

  PBMCs from patients were isolated using 50 mL Leucosep™ tubes (Greiner Bio-One International, Germany) and Ficoll-Paque™ PLUS (GE Healthcare, Sweden). Whole blood drawn into sodium heparin blood collection tubes were diluted 3x with phosphate-buffered saline (PBS) without calcium or magnesium (Lonza, Walkersville, MD). Diluted cell suspensions were carefully layered on Leucosep tubes and centrifuged for 15 minutes at 800 x g at room temperature (RT). Interphase containing PBMCs were harvested and washed with PBS and subsequently centrifuged for 10 minutes at 250 x g at RT before further processing.

  Study EGAS00001004229

• Elucidation of molecular mechanism of NAFLD-HCC

  We aimed to elucidate the interaction between cancer cells and immune cells in the tumor immune microenvironment of non-viral hepatocellular carcinoma.

  Study JGAS000311

• Siberia.Pakendorf

  The tar archive contains a) the txt file with the genotypes, b) illumina annotation file with info on SNPs, c) sample info file unfiltered illumina data, autosomes only data from Pugach et al MBE 2016 The Complex Admixture History and Recent Southern Origins of Siberian Populations

  Dataset EGAD00010002304

• Deep sequencing of the gut microbiome from donors of the Milieu Intérieur cohort

  This dataset includes 1,359 paired-end shotgun metagenomics samples from 946 healthy donors of the Milieu Intérieur cohort. 413 of the donors provided two samples (V1 and V2).

  Dataset EGAD00001006554

• Flemish_Gut_Flora_Project

  "Here, we studied well-phenotyped individuals from the Flemish Gut Flora Project (FGFP, N=1,106, Belgium) and the effect of environments on microbiome."

  Study EGAS00001001689

• SCLC ctDNA sequencing

  In this study we have sequenced the ctDNA of 28 Small Cell Lung Cancer patients in the TP53 gene, each sample has been sequenced twice.

  Study EGAS00001003984

• SCC ctDNA sequencing

  In this study we have sequenced the ctDNA of 28 Squamous Cell Carcinoma patients in the TP53 gene, each sample has been sequenced twice.

  Study EGAS00001003987

• MalariaGEN case-control study in the Gambia

  MalariaGEN case-control study in the Gambia.

  Study EGAS00000000026

• DAC for sputum fungal microbiome data

  Dac EGAC00001003006

• DAC for Oncogenomics QIMR Berghofer

  Dac EGAC00001001088

• Data Access Committee for WES RCC

  Dac EGAC00001003161

• DAC for study Vel Exome Sequencing

  Dac EGAC00001000012

• DAC for Sardinia FACS pilot project

  Dac EGAC00001000132

• DAC for study POT1 splice

  Dac EGAC00001000184

• DAC for SNP phenotyping Kiel

  Dac EGAC00001000316

• DAC for Mesothelioma Genomics Study

  Dac EGAC00001000615

• DAC for Human Stem Sell Sequencing

  Dac EGAC00001000642

• DAC for studying early onset IBD

  Dac EGAC00001000840

• DAC for Familial Breast Cancer study EGAS00001003305

  Dac EGAC00001001087

• DAC for genentech GBC study

  Dac EGAC00001001155

• Department for BioMedical Research, University of Bern

  Dac EGAC00001001457

• DAC for Gastric Adenocarcinoma Heterogeneity study

  Dac EGAC00001001649

• Data Access Committee for IMBA

  Dac EGAC00001001690

• Data Access Committee for data from EGAS00001005174

  Dac EGAC00001002059

• Data Access Committee for data from EGAS00001005395

  Dac EGAC00001002183

• Data Access Committee for PPIL4 Paper

  Dac EGAC00001002301

• Data Access Committee for Massim study

  Dac EGAC00001002522

• Data Access Committee for Institut Curie

  Dac EGAC00001002711

• Data Access Committee for Pediatric Medulloblastoma

  Dac EGAC00001002896

• Institute for Surgical Pathology

  Dac EGAC00001002949

• Data Access Commitee for MNP2

  Dac EGAC00001003033

• DAC for Karolinska Institute REM Lab

  Dac EGAC00001003142

• DAC for Kotsch/Lukassen/Conrad labs

  Dac EGAC00001003464

• Data Access Committee for data from EGAS00001002864

  Dac EGAC00001003487

• Data Access Committee for data from EGAS00001007832

  Dac EGAC00001003500

• Data Access Committee for data from EGAS00001007819

  Dac EGAC00001003501

• Data Access Committee for data from EGAS00001007904

  Dac EGAC00001003512

• Data Access Committee for data from EGAS00001008107

  Dac EGAC00001003568

• UCL Centre for Longitudinal Studies

  Dac EGAC00001001041

• BAP1 Project

  For our BAP1 manuscript

  Dac EGAC50000000006

• EGAD00010000608

  SNP6 data for seminoma samples

  Dataset EGAD00010000608

• Swedish Bipolar Disorder exome sequencing (SWEBIC)

  This research project was a collaboration between the Karolinska Institute and the Stanley Center at the Broad Institute. In this project we sequenced and analyzed the whole exomes of 5340 SWEBIC Bipolar case samples from collaborators in Sweden. Genomic DNA from each samples was sequenced to a mean depth of 20x. The exome used Twist capture and samples were sequenced on Illumina HiSeqX machines producing CRAM files.

  Dataset EGAD50000001123

• Whole-genome sequencing of the parental tumor and established organoids from a patient with gastric-type cervical adenocarcinoma

  This study aims to evaluate the genetic characteristics of patient-derived organoids established from gastric-type cervical adenocarcinoma and to assess their similarity to the parental tumors using whole-genome sequencing.

  Study JGAS000796

• Combined DNA Methylation and Genotyping via scTAMARA-seq (DNA)

  This dataset features single-cell DNA methylation and nuclear genotyping data obtained using the scTAMARA-seq protocol, a combination of SDR-seq and scTAM-seq. The targeted panel, 200 DNA methylation (a subset of the orginal 448 CpG targets) and 167 genotyping targets, were applied to a CD34+ enriched bone marrow sample from patient X.1. The data was generated on the Mission Bio Tapestri platform.

  Dataset EGAD00001015496

• Solution-based exome capture and HiSeq2000-based massively parallel sequencing of Follicular Lymphoma

  A cohort of follicular lymphoma cases had tumor cells purified from tissue samples after informed consent using flow cytometry. DNA was extracted from the cells, and samples were subjected to solution-based exome capture using the Illumina TruSeq Exome Enrichment Kit and the Illumina HiSeq 2000 platform.

  Study phs000729

• Whole exome and ChIP sequencing of external auditory canal squamous cell carcinoma (EACSCC)

  We performed whole exome sequencing of the primary tumor tissues, peripheral blood mononuclear cells from an EACSCC patient as well as the cell line established from the primary tumor tissues. We performed ChIP sequencing of primary tumor tissues and noncancerous ear skin tissues from EACSCC patients as well.

  Study JGAS000645