17304 results for "fc 26 coins Buyfc26coins.com is EA Sports official for FC 26 coins They are definitely a top seller..rG5l"

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• 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

• BRACOVID_phenotype_basic

  Basic phenotypes for BRACOVID cohort.

  Dataset EGAD00001007832

• Hostage_1_phenotype_basic

  Basic phenotypes for Hostage1 cohort.

  Dataset EGAD00001007838

• GEN_COVID_phenotype_basic

  Basic phenotypes for GEN_COVID cohort.

  Dataset EGAD00001007836

• 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_lab

  Lab values for GEN_COVID cohort.

  Dataset EGAD00001007837

• Hostage_3_phenotype_lab

  Lab values for Hostage3 cohort.

  Dataset EGAD00001007843

• Exome

  Exome Seq for Study EGAS00001001844

  Dataset EGAD00001002159

• Hostage_4_phenotype_lab

  Lab values for Hostage4 cohort.

  Dataset EGAD00001007845

• INMUNGEN_CoV2_phenotype_lab

  Lab values for INMUNGEN_CoV2 cohort.

  Dataset EGAD00001007847

• SPGRX_phenotype_basic

  Basic phenotypes for SPGRX cohort.

  Dataset EGAD00001007848

• SC_DDD-G-3

  Unfiltered genotype data for DDD Study trios (patient and parents) (N=2,166 samples), some of which were used for replication of neurodevelopmental disorder polygenic risk (Niemi et al., Nature 2018). Samples were genotyped on the Illumina HumanOmniExpress BeadChip

  Dataset EGAD00010001602

• Blood Handling and Leukocyte Isolation Methods Impact the Global Transcriptome of Immune Cells

  In order to characterize the effects of upstream sample handling on the transcriptome of isolated leukocyte populations, we simulated various sample handling methods on whole blood prior to leukocyte isolation for low-input RNA-sequencing.

  Study phs001563

• Ultrasensitive Profiling of UV Mutations in Facial Tumors in TSC

  In this study we searched for mutations in the TSC2 and TP53 genes in sample sets from individuals with Tuberous Sclerosis Complex (TSC) and from subjects without TSC. The study was focused on the analysis of TSC facial angiofibroma.

  Study phs002914

• Whole Exome Sequencing of Parathyroid Cancer Identifies Candidate Driver Mutations and Core Pathways

  Here we performed genomic characterization of twenty-nine sporadic parathyroid cancers using next generation whole exome sequencing. Thirty-three novel candidate driver genes for sporadic parathyroid cancer were proposed, in addition to previously known driver genes CDC73 and MEN1.

  Study phs001765

• Systematic Analysis of Coding and Non-coding Elements in Developmental Pathways Implicated in Holoprosencephaly Pathogenesis

  We applied targeted capture to examine 153 genes representative of all the major vertebrate developmental pathways among 340 probands and 285 of their unaffected parents to rank their relative significance as causes for holoprosencephaly (HPE).

  Study phs001653

• An Omics View of Asthma through Monozygotic Twins

  The etiology of asthma involves both genetic and non-genetic factors. We performed whole transcriptome sequencing on monozygotic twins discordant or concordant for asthma (with concordant healthy twins as controls), and identified multiple potential transcriptomic profiles associated with the asthma phenotype.

  Study phs000886

• Single Cell ATAC-Seq of MELAS

  This dataset includes combined single Assay for Transposase-Accessible Chromatin, using sequencing (ATAC-seq), and mitochondrial DNA sequencing of peripheral blood mononuclear cells from three individuals with m.3243A>G associated MELAS (Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like episodes).

  Study phs002217

• scRNAseq and scTCRseq of three tumor lesions derived from one patient receiving adoptive TIL therapy

  scRNA sequencing and scTCR sequencing on three tumor lesions derived from one patient receiving adoptive tumor-infiltrating lymphocyte (TIL) therapy. Expanded metastasis was used for TIL expansion and yielded the TIL product which also was used for scTCR sequencing. 10 weeks after transfer of the TIL product the regressing metastasis was resected. After the patient progressed the progressing metastasis was removed (61 weeks).

  Dataset EGAD50000000406

• ST dataset from subcortical white matter MS lesions (CA & CI) and controls

  This dataset contains the FASTQ files, the correspondent H&E pictures with the fiducial frames and the json files that were used for the spatial transcriptomic analysis in our paper (n=19). Within the json files names, one can find the information about the slide name (V11M111-111) and the capture area (A1) for each sample.

  Dataset EGAD50000000520