17871 results for "the best way to get coins in fc 26 Navštivte Buyfc26coins.com Společnost známá transparentními transakcemi..CQ2q"

in 24.22 milliseconds.

• Genome-wide analysis for non alcoholic fatty liver disease

  Genome-wide association study for the 902 patients of non alcoholic fatty liver disease (NAFLD) including non alcoholic steato hepatitis (NASH) and hepatocellurar carcinoma and 7672 controls.

  Study JGAS000126

• BCG-Flu Challenge Study Human RNA-seq

  Whole blood RNA sequencing data generated from human samples collected as part of the BCG-Flu Challenge study. The dataset includes 746 samples. Paired-end sequencing was performed on an Illumina NovaSeq 6000 platform with a 150 bp paired-end configuration. Raw FASTQ files are provided.

  Dataset EGAD50000002407

• LUAD dataset

  This dataset includes 25 LUAD samples consisting of control samples derived from lymph node and tumor tissues samples, which were either untreated or treated with formalin and/or the NEBNext FFPE DNA Repair v2 Module. Sequencing was performed on the Illumina NovaSeq X platform using a 2×150 nt configuration, yielding approximately 18 Gbp per sample.

  Dataset EGAD50000001950

• 10x single-nucleus RNA-seq of postoperative human FCD II brain tissues

  This dataset contains 10x Genomics single-nucleus RNA sequencing data from postoperative brain tissues of patients with focal cortical dysplasia type II (FCD II). The samples were processed using the Chromium platform.

  Dataset EGAD50000001403

• Oxford Nanopore WGS

  A total of 20 individuals, were analyzed using Oxford Nanopore Technologies long-read sequencing. Each individual was sequenced on one PromethION flow-cell, providing approximately 25-30X coverage of the genome. The data is deposited as nanopore BAM files with methylation information included.

  Dataset EGAD50000000573

• Single-cell/single-nucleus RNA-seq of diffuse hemispheric gliomas, H3G34-mutant.

  9 DHG-H3G34 patient samples were sequenced by paired-end scRNA-sequencing using the Smart-Seq2 protocol on a NextSeq 500 sequencer (Illumina). Illumina bcl2fastq 1.5 was used for demultiplexing. This dataset contains the resulting 9,408 fastq files of 4,704 single cells/nuclei sequenced.

  Dataset EGAD50000000760

• RNA sequencing

  For RNA sequencing: All sample numbers starting with 6717 are tumor samples which has been sequenced using transcriptomics (see BAM files). It concerns biopsies of metastatic lesions from patients with BRAFV600 mutated melanoma, obtained before, during and after the study treatment (see samples metadata). RNA sequencing is performed using the Illumina Novaseq 6000 system.

  Dataset EGAD50000000383

• IBS-D RNA-seq raw data

  The data set consists of fastq raw files from RNA-seq of seven mucosal biopsies of the colon from seven patients, among them three patients with irritable bowel syndrome with diarrhea-predominant symptoms. Paired end sequencing on Illumina NovaSeq 6000 was used.

  Dataset EGAD50000000063

• NICOLA QUB Genetic

  Blood-derived DNA was obtained from samples within the NICOLA cohort. Genetic data was generated using the Illumina Infinium CoreExome-24 array (Illumina, USA) and is available for 2,978 participants (551,839 directly genotyped and 18,148,478 imputed single nucleotide polymorphisms following initial quality control). Genetic .bed .bim and .fam files are available.

  Dataset EGAD00010002762

• Combined genetic and transcriptome analysis of patients with Systemic Lupus Erythematosus (SLE)

  A comprehensive profiling of the genomic architecture of Systemic Lupus Erythematosus (SLE) by combining genetic and transscriptomic analysis by RNA-seq.

  Study EGAS00001003662