1248 results for ""halted+early"+"slower-than-anticipated+enrollment"+hospitalized+oral+adaptive+platform"

in 5.87 milliseconds.

• UOXFi008-B / SAMEA103887561 WGS data

  The iPSC line UOXFi008-B / SAMEA103887561 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 UOXFi008-B is available for research use at www.EBiSC.org.

  Dataset EGAD50000001089

• EDi016-C / SAMEA4768168 WGS data

  The iPSC line EDi016-C / SAMEA4768168 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 EDi016-C is available for research use at www.EBiSC.org.

  Dataset EGAD50000001090

• EDi019-B / SAMEA4776418 WGS data

  The iPSC line EDi019-B / SAMEA4776418 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 EDi019-B is available for research use at www.EBiSC.org.

  Dataset EGAD50000001091

• UKKi019-A / SAMEA17624668 WGS data

  The iPSC line UKKi019-A / SAMEA17624668 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 UKKi019-A is available for research use at www.EBiSC.org.

  Dataset EGAD50000001094

• UKKi019-B / SAMEA17626168 WGS data

  The iPSC line UKKi019-B / SAMEA17626168 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 UKKi019-B is available for research use at www.EBiSC.org.

  Dataset EGAD50000001096

• Saliva Microbiota of Finnish children from the PANIC study

  Saliva microbiota of 407 participants of PANIC study, is profiled with 16S rRNA gene sequencing (regions V3-V4). Amplification was performed using the TruSeq-switched tail amplicons. The sequencing was performed using the 2 × 301 base-pair on the Illumina MiSeq PE300 platform. Data includes information on sex, age, and caries status of participants. File format is fastq.gz.

  Dataset EGAD50000000989

• WGA_Fulani_Database

  In total, 329 DNA samples were genotyped on the Illumina Infinium H3Africa Consortium array (designed for 2,271,503 SNPs; using BeadChip type: H3Africa_2019_20037295_B1). Genotyping was performed at the SNP&SEQ Technology Platform (NGI/SciLifeLab Genomics, Sweden). WGA Fulani dataset includes individuals from the following populations: 33 BurkinaFaso_FulaniBanfora, 32 BurkinaFaso_FulaniTindangou, 33 Mali_FulaniDiafarabe, 35 Cameroon_FulaniTcheboua, 34 Chad_FulaniBongor, 24 Chad_FulaniLinia, 25 Niger_FulaniAbalak, 32 Niger_FulaniAder, 31 Niger_FulaniDiffa, 20 Niger_FulaniBalatungur, and 30 Niger_FulaniZinder.

  Dataset EGAD50000000654

• Long read sequencing to detect structural variants in Indian patient with non-syndromic autism spectrum disorders

  This study involved performing long read whole genome sequencing using Oxford Nanopore Technology platform on to detect causative structural variants in patients with non-syndromic autism spectrum disorder. This study was performed on 23 such children in whom prior karyotyping, Fragile-X analysis (in males), chromosomal microarray and whole exome sequencing did not identify a causative variant.

  Dataset EGAD50000001231

• RNA-Seq profiles from the CheckMate-649 Clinical Trial

  This dataset contains RNA sequencing (RNAseq) data of 814 patients from the CheckMate 649 clinical trial whose ICF allows data deposition into a public repository. Gene expression profiling was performed retrospectively using RNAseq on a subset of baseline tumor samples. Paired-end FASTQ files were processed on Seven Bridges platform (Seven Bridges Genomics).

  Dataset EGAD50000001105

• RNA-sequencing of platelets and immortalized megakaryocyte cell lines for inherited thrombocytopenia

  Total RNA-sequencing of platelets and immortalized megakaryocyte cell lines for inherited thrombocytopenia. Libraries were prepared using Illumina TruSeq Stranded Total RNA with Ribo-Zero Gold kits. The samples were paired-end sequenced using the NovaSeq 6000 platform at a depth of 60 million reads per sample with a read length of 100 base pairs.

  Dataset EGAD50000001818