17198 results for "free coins in fc 26 Visit Buyfc26coins.com for latest FC 26 coins news..xwWa"

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• SPGRX_phenotype_basic

  Basic phenotypes for SPGRX cohort.

  Dataset EGAD00001007848

• Cancer Alliance Exome

  Exome sequencing for individualized cancer interpretation

  Dataset EGAD00001006236

• Hostage_2_phenotype_basic

  Basic phenotypes for Hostage2 cohort.

  Dataset EGAD00001007840

• Hostage_1_phenotype_lab

  Lab values for Hostage1 cohort.

  Dataset EGAD00001007839

• BelCovid_2_phenotype_lab

  Lab values for BelCovid2 cohort.

  Dataset EGAD00001007835

• Hostage_3_phenotype_basic

  Basic phenotypes for Hostage3 cohort.

  Dataset EGAD00001007842

• Hostage_4_phenotype_lab

  Lab values for Hostage4 cohort.

  Dataset EGAD00001007845

• BRACOVID_phenotype_basic

  Basic phenotypes for BRACOVID cohort.

  Dataset EGAD00001007832

• Hostage_1_phenotype_basic

  Basic phenotypes for Hostage1 cohort.

  Dataset EGAD00001007838

• BRACOVID_phenotype_lab

  Lab values for BRACOVID cohort.

  Dataset EGAD00001007833

• Hostage_2_phenotype_lab

  Lab values for Hostage2 cohort.

  Dataset EGAD00001007841

• BelCovid_2_phenotype_basic

  Basic phenotypes for BelCovid2 cohort.

  Dataset EGAD00001007834

• GEN_COVID_phenotype_basic

  Basic phenotypes for GEN_COVID cohort.

  Dataset EGAD00001007836

• GEN_COVID_phenotype_lab

  Lab values for GEN_COVID cohort.

  Dataset EGAD00001007837

• Hostage_3_phenotype_lab

  Lab values for Hostage3 cohort.

  Dataset EGAD00001007843

• Hostage_4_phenotype_basic

  Basic phenotypes for Hostage4 cohort.

  Dataset EGAD00001007844

• INMUNGEN_CoV2_phenotype_basic

  Basic phenotypes for INMUNGEN_CoV2 cohort.

  Dataset EGAD00001007846

• INMUNGEN_CoV2_phenotype_lab

  Lab values for INMUNGEN_CoV2 cohort.

  Dataset EGAD00001007847

• Exome

  Exome Seq for Study EGAS00001001844

  Dataset EGAD00001002159

• Born in Bradford (BiB)

  Dac EGAC00001003494

• Whole exome sequencing of pediatric soft tissue sarcoma PDX models

  Childhood cancer remains one of the leading causes of death in pediatric patients in Europe. Pediatric sarcomas, comprising soft tissue sarcomas and malignant bone tumors, are a heterogenous group of malignancies, with more than 50 subtypes (WHO classification). Due to low case numbers, studying pediatric sarcomas requires accurate and reliable preclinical models. Here, we established 18 soft tissues sarcoma PDX models, including Ewing Sarcoma, Rhabdmyosarcoma and Osteosarcoma. We characterized these models by Whole Exome Sequencing and assessd the response to a wide range of drugs.

  Study EGAS50000000048

• Clinical and Genetic Analysis of Costa Rican Patients with Parkinson's Disease

  This study is a pilot study designed to describe the clinical and genetic landscape of Parkinson's disease in Costa Rica. While most genetic studies have been conducted on Europeans, few have examined Parkinson's disease in Costa Ricans. 118 patients and 97 controls were recruited at the Movement Disorders Unit of the Department of Neurology, Hospital San Juan de Dios, Caja Costarricense de Seguro Social, Costa Rica. Familial Parkinson's disease genes were sequenced using Next-Generation Sequencing. We also measured and obtained different sociodemographic and clinical information.

  Study phs002495

• Cancer Genetic Markers of Susceptibility (CGEMS) Prostate Cancer Genome-Wide Association Study (GWAS) - Primary Scan (Stage 1) - PLCO Screening Trial

  The Cancer Genetic Markers of Susceptibility (CGEMS) prostate cancer genome-wide association study (GWAS) included genotyping approximately 550,000 SNPs (Phase 1A with HumanHap300 and Phase 1B HumanHap240, both from Illumina, San Diego, CA) in 1,172 prostate cancer patients and 1,157 controls of European ancestry from the Prostate, Lung, Colon and Ovarian (PLCO, http://www.cancer.gov/prevention/plco/) Cancer Screening Trial. The original analysis published in Nature Genetics [PMID: 17401363] included 2,282 subjects. After improvement and revisions of the original analysis, 2,252 subjects were submitted to dbGaP.

  Study phs000207

• Whole exome sequencing of 184 unrelated subjects with 22q11.2 deletion syndrome (DiGeorge syndrome/velo-cardio-facial syndrome)

  Our goal is to find genetic modifiers of major phenotypes in patients with 22q11.2 deletion syndrome, also known as DiGeorge syndrome or velo-cardio-facial syndrome. Whole exome sequencing was performed as part of a contract to the NHLBI, Resequencing and Genotyping Service. We have obtained cardiac phenotype information from the de-identified subjects enrolled in the study, either by echocardiography report or medical doctor report. All of the subjects have a 3 million base pair 22q11.2 deletion flanked by low copy repeats, LCR22, A-D.

  Study phs000987

• Next Generation Mendelian Genetics: Ehlers-Danlos Syndrome Type VIII

  The NHGRI Next Generation Mendelian Genetics project uses exome resequencing to identify variants in unsolved Mendelian diseases. Ehlers-Danlos syndrome Type VIII is a dominantly inherited connective tissue disorder that is distinguished from other forms of EDS by significant early-onset periodontal disease. Although the clinical phenotype is well delineated, the underlying molecular basis remains unknown. By studying a large family of affected and unaffected individuals with the EDS VIII by exome sequencing, we hope to identify unique regions of homology to assist in identifying the causative gene.

  Study phs000540