12162 results for "fc 26 coins pc Visit Buyfc26coins.com for latest FC 26 coins news..z7ux"

in 65.68 milliseconds.

• EDi018-C / SAMEA4774168 WGS data

  The iPSC line EDi018-C / SAMEA4774168 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line EDi018-C is available for research use at www.EBiSC.org.

  Dataset EGAD50000001081

• EDi018-B / SAMEA4773418 WGS data

  The iPSC line EDi018-B / SAMEA4773418 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line EDi018-B is available for research use at www.EBiSC.org.

  Dataset EGAD50000001080

• UOXFi007-A / SAMEA103988274 WGS data

  The iPSC line UOXFi007-A / SAMEA103988274 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line UOXFi007-A is available for research use at www.EBiSC.org.

  Dataset EGAD50000001079

• RCi007-C / SAMEA4084916 WGS data

  The iPSC line RCi007-C / SAMEA4084916 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line RCi007-C is available for research use at www.EBiSC.org.

  Dataset EGAD50000001072

• RCi005-A / SAMEA3961534 WGS data

  The iPSC line RCi005-A / SAMEA3961534 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line RCi005-A is available for research use at www.EBiSC.org.

  Dataset EGAD50000001071

• RCi004-B / SAMEA3106205 WGS data

  The iPSC line RCi004-B / SAMEA3106205 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line RCi004-B is available for research use at www.EBiSC.org.

  Dataset EGAD50000001070

• RCi004-A / SAMEA3106011 WGS data

  The iPSC line RCi004-A / SAMEA3106011 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line RCi004-A is available for research use at www.EBiSC.org.

  Dataset EGAD50000001069

• UKKi018-C / SAMEA103988380 WGS data

  The iPSC line UKKi018-C / SAMEA103988380 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line UKKi018-C is available for research use at www.EBiSC.org.

  Dataset EGAD50000001067

• EDi015-B / SAMEA4459375 WGS data

  The iPSC line EDi015-B / SAMEA4459375 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line EDi015-B is available for research use at www.EBiSC.org.

  Dataset EGAD50000001066

• EDi013-C / SAMEA4459368 WGS data

  The iPSC line EDi013-C / SAMEA4459368 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line EDi013-C is available for research use at www.EBiSC.org.

  Dataset EGAD50000001065

• EDi012-C / SAMEA4459364 WGS data

  The iPSC line EDi012-C / SAMEA4459364 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line EDi012-C is available for research use at www.EBiSC.org.

  Dataset EGAD50000001064

• EDi012-B / SAMEA4459363 WGS data

  The iPSC line EDi012-B / SAMEA4459363 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line EDi012-B is available for research use at www.EBiSC.org.

  Dataset EGAD50000001063

• UKKi017-C / SAMEA17621668 WGS data

  The iPSC line UKKi017-C / SAMEA17621668 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line UKKi017-C is available for research use at www.EBiSC.org.

  Dataset EGAD50000001061

• EDi013-A / SAMEA4459365 WGS data

  The iPSC line EDi013-A / SAMEA4459365 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line EDi013-A is available for research use at www.EBiSC.org.

  Dataset EGAD50000001057

• EDi010-B / SAMEA4459356 WGS data

  The iPSC line EDi010-B / SAMEA4459356 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line EDi010-B is available for research use at www.EBiSC.org.

  Dataset EGAD50000001056

• RBi001-A / SAMEA3368212 WGS data

  The iPSC line RBi001-A / SAMEA3368212 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line RBi001-A is available for research use at www.EBiSC.org.

  Dataset EGAD50000001058

• RCi006-A / SAMEA3962402 WGS data

  The iPSC line RCi006-A / SAMEA3962402 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line RCi006-A is available for research use at www.EBiSC.org.

  Dataset EGAD50000001059

• BIONi010-B / SAMEA3158000 WGS data

  The iPSC line BIONi010-B / SAMEA3158000 has undergone whole genome sequencing. Whole genome sequencing was done using Illumina HiSeq X Five platform with a reference genome of GRCh38. Raw data as FASTQ files and analysed data as CRAM files are available for this sample, in this dataset. The iPSC line BIONi010-B is available for research use at www.EBiSC.org.

  Dataset EGAD50000001055

• Single-sell RNA sequencing counts from 7 acute myeloid leukemia patients and 3 healthy donors

  This dataset contains count data (from 10X CellRanger) and metadata from 7 acute myeloid leukemia subjects treated with chemotherapy, as well as data from 3 healthy donors. Additionally, the dataset includes VDJ data for all subjects except for 31_base and the 3 healthy donors (TCRseq not performed).

  Dataset EGAD50000000525

• Sensitive urothelial cancer detection via high volume urine DNA analysis

  We developed a high volume (100 mL) urine DNA collection kit and laboratory platform (UroScout) analyzing 25 commonly mutated UC genes and 8 copy number-altered loci for urine tumor DNA (utDNA) alterations. To assess accuracy of UC detection, we analyzed 498 urine samples from diagnostic and surveillance timepoints from 193 UC patients and 88 cancer-negative patients evaluated for UC.

  Dataset EGAD50000000891

• Single-cell RNA sequencing of 16 NPM1 mutated AML patients

  This dataset contains paired-end fastq files for single-cell RNA-seq of 16 NPM1 mutated AML patients. 19 fastq pairs are included, with two samples split into two lanes and a second (technical) replicate for one patient. Libraries were constructed using 10x Genomics Chromium Next GEM Single cell 3’ v3.1 and sequencing was performed using Illumina NovaSeq6000.

  Dataset EGAD50000000478

• Whole Exome Sequences from Eivissan and Menorcan Individuals

  30 and 21 whole exome sequences for Eivissan and Menorcan healthy unrelated volunteers, respectively. The exomes were captured with the Agilent SureSelect Human All Exon V6 capture kit and pair-end sequenced in Illumina platforms. For each individual, a pair of ".fastq" files can be found containing the raw reads.

  Dataset EGAD50000000620

• Comprehensive NGS Profiling to Enable Detection of ALK Gene Rearrangements and MET Amplifications in Non-Small Cell Lung Cancer

  We evaluate the analytical performance of the PGDx™ elio™ tissue complete assay, a 505 gene next-generation sequencing (NGS) tissue-based assay, that has now been FDA-cleared for use by physicians to help guide treatment decisions for cancer patients, using a NSCLC cohort of 38 patients.

  Dataset EGAD50000000016

• MB_COMICS_Methylome

  Medulloblastoma (MB) is the most common malignant brain tumor in children. It is a neuroectodermal tumor located in the cerebellum. International consensus recognizes four distinct subgroups of MBs including Wingless (WNT), Sonic Hedgehog (SHH), Group 3 (G3), and Group 4 (G4) with distinct molecular characteristics, prognoses, and mortality rates in patients. Here, we have compiled and evaluated a large international MB cohort for which we generated methylome data for 369 primary MB patient samples.

  Dataset EGAD00010002669

• InterPregGen-GWAS-UZB-2

  GWAS genotype data for maternal and fetal (baby) cases of preeclampsia and controls from Uzbekistan. This dataset is a component of the InterPregGen FP7 project. DNA samples for this component were collected by InterPregGen Consortium members in Tashkent, Uzbekistan at the Institute of Immunology, Uzbek Academy of Sciences and at the Republic Specialized Scientific Practical Medical Centre of Obstetrics and Gynecology

  Dataset EGAD00010001917