567 results for "24版指南"

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• Whole exome DNA sequencing pre-treatment on tumor samples (n=24) matched with blood samples (n=24)

  Data from NABUCCO cohort 1 (NCT03387761). This dataset includes Whole exome DNA sequencing on bladder tumor samples (n=24) matched with blood samples (n=24). The data is pre-treatment.

  Dataset EGAD00001006850

• Characterization of Arabian Peninsula whole exomes

  We conducted whole exome sequencing (using the SureSelect Human All Exon V5 + UTRs target enrichment kit) of 90 individuals from AP (23 from Saudi Arabia, 24 from Yemen, 24 from Oman and 19 from UAE).

  Study EGAS00001006487

• PDX-OmniExpress24

  Primary and PDX SqCC samples using Infinium OmniExpress-24

  Dataset EGAD00010001228

• RHD_SA_HC24_Controls

  Healthy volunteers recruited in Samoa

  Dataset EGAD00010000963

• macIDR validation data

  RNA-seq of 24 M-CSF differentiated human peripheral monocyte-derived macrophages (MDMs) activated with short exposure (3hours) to LPS, or long exposure (24 hours) to LPS, LPS with IFNγ, IFNγ, IL-4, IL-10, and dexamethasone.

  Dataset EGAD00001004584

• single-cell RNA-seq Case-Control study of children progressing to Type1 diabetes

  Single-cell RNA sequencing was carried out on four selected PBMC samples of Finnish children at risk of developing Type 1 diabetes and their gender age and HLA matched control children using 10X genomic platform. All four Case children were positive for multiple islet specific autoantibodies and two of them also progressed to clinical disease during the follow up whereas the control children remain negative for all autoantibodies. Age at seroconversion for Case 2, 3, 5, and 9 children is 12, 18, 24, and 18 months, respectively. Age at sampling, in months, for the pairs was as follows (Case/Control): pair 2:24/24; pair 3: 12/18; pair 5: 12/12; pair 9:24/18.

  Study EGAS00001004070

• TTN gene targeted sequencing for AMC cohort

  TTN gene targeted sequencing for AMC cohort (n=24)

  Dataset EGAD00001005497

• Targeted capture ctDNA Library CRCQV42Run021-24

  Targeted capture ctDNA Library CRCQV42Run021-24 from patient PBC0001653, saliva sample

  Dataset EGAD00001010445

• Targeted capture ctDNA Library CRCQV42Run026-24

  Targeted capture ctDNA Library CRCQV42Run026-24 from patient PBC0005064, saliva sample

  Dataset EGAD00001010495

• Targeted capture ctDNA Library CRCQV42Run050-24

  Targeted capture ctDNA Library CRCQV42Run050-24 from patient PBC0002494, buffy coat sample

  Dataset EGAD00001010797

• Targeted capture ctDNA Library CRCQV42Run020-24

  Targeted capture ctDNA Library CRCQV42Run020-24 from patient PBC0001310, plasma baseline sample

  Dataset EGAD00001010429

• Targeted capture ctDNA Library CRCQV42Run023-24

  Targeted capture ctDNA Library CRCQV42Run023-24 from patient PBC0002383, saliva sample

  Dataset EGAD00001010464

• Targeted capture ctDNA Library CRCQV42Run031-24

  Targeted capture ctDNA Library CRCQV42Run031-24 from patient PBC0001470, buffy coat sample

  Dataset EGAD00001010534

• Targeted capture ctDNA Library CRCQV42Run039-24

  Targeted capture ctDNA Library CRCQV42Run039-24 from patient PBC0001413, plasma baseline sample

  Dataset EGAD00001010619

• Targeted capture ctDNA Library CRCQV42Run047-24

  Targeted capture ctDNA Library CRCQV42Run047-24 from patient PBC0002989, buffy coat sample

  Dataset EGAD00001010735

• Targeted capture ctDNA Library CRCQV42Run048-24

  Targeted capture ctDNA Library CRCQV42Run048-24 from patient PBC0005531, buffy coat sample

  Dataset EGAD00001010756

• SNParray_ASD

  ASD samples using Illumina Infinium Human Core-24 BeadChip platform

  Dataset EGAD00010002229

• Targeted capture ctDNA Library CRCQV42Run035-24

  Targeted capture ctDNA Library CRCQV42Run035-24 from patient PBC0004565, plasma 9 month sample

  Dataset EGAD00001010588

• Targeted capture ctDNA Library CRCQV42Run041-24

  Targeted capture ctDNA Library CRCQV42Run041-24 from patient PBC0005116, plasma 3 month sample

  Dataset EGAD00001010633

• Targeted capture ctDNA Library CRCQV42Run036-24

  Targeted capture ctDNA Library CRCQV42Run036-24 from patient PBC0001328, plasma 36 month sample

  Dataset EGAD00001010602

• Targeted capture ctDNA Library CRCQV42Run043-24

  Targeted capture ctDNA Library CRCQV42Run043-24 from patient PBC0002329, plasma 3 month sample

  Dataset EGAD00001010653

• Targeted capture ctDNA Library CRCQV42Run051-24

  Targeted capture ctDNA Library CRCQV42Run051-24 from patient PBC0001319, buffy coat sample

  Dataset EGAD00001010817

• Targeted capture ctDNA Library CRCQV42Run029-24

  Targeted capture ctDNA Library CRCQV42Run029-24 from patient PBC0003334, plasma 3 month sample

  Dataset EGAD00001010517

• Targeted capture ctDNA Library CRCQV42Run044-24

  Targeted capture ctDNA Library CRCQV42Run044-24 from patient PBC0005531, plasma 9 month sample

  Dataset EGAD00001010674

• Targeted capture ctDNA Library CRCQV42Run045-24

  Targeted capture ctDNA Library CRCQV42Run045-24 from patient PBC0001409, plasma 3 month sample

  Dataset EGAD00001010695

• Targeted capture ctDNA Library CRCQV42Run046-24

  Targeted capture ctDNA Library CRCQV42Run046-24 from patient PBC0002494, plasma 3 month sample

  Dataset EGAD00001010715

• Neutrophils infected with Leishmania donovani

  In the context of studying visceral leishmaniasis, neutrophils infected with Leishmania donovani have been compared to uninfected neutrophils. Compared time points are 0, 6 and 24 hours post infection. Neutrophils of three human donors have been used. Overall 6 samples for infected neutrophils at time point 6 hours and 6 samples for infected neutrophils at time point 24 hours exist, including three biological samples and two technical samples. Uninfected neutrophils represent 3 samples at time point 0 hours, 3 samples at time point 6 hours and 3 samples at time point 24 hours. Transcriptome of Leishmania donovani culture has been assessed in two replicates.

  Study EGAS00001004912

• Targeted capture ctDNA Library CRCQV34Run007-24

  Targeted capture ctDNA Library CRCQV34Run007-24 from patient PBC0001051, TNBC FFPE sample

  Dataset EGAD00001010361

• Targeted capture ctDNA Library CRCQV34Run015-24

  Targeted capture ctDNA Library CRCQV34Run015-24 from patient PBC0002255, TNBC FFPE sample

  Dataset EGAD00001010385

• Targeted capture ctDNA Library CRCQV42Run017-24

  Targeted capture ctDNA Library CRCQV42Run017-24 from patient PBC0002294, TNBC FFPE sample

  Dataset EGAD00001010414

• Targeted capture ctDNA Library CRCQV42Run034-24

  Targeted capture ctDNA Library CRCQV42Run034-24 from patient PBC0001396, TNBC FFPE sample

  Dataset EGAD00001010572

• PACA-CA kras_deep_sequencing alignments in support of PACA-CA ICGC Release 24

  ICGC DCC Release 24, PACA-CA Deep KRAS sequencing

  Dataset EGAD00001003263

• Single cell RNA-seq of 24 samples from 13 individual human embryonic meninges of PCW 5.0-13.0 using 10X chromium technology

  A total of 24 samples of meninges from 13 normal human embryos of post-conceptional week (PCW) 5.0-13.0 were dissected and subject to 10Xgenomics chromium single cell RNA sequencing with the purpose of identifying cell types and gene expression programs for normal meninges development. All libraries were sequenced on an Illumina NovaSeq 6000 using S4 to a target sequencing depth of 100,000 reads/cell. Final data after processing with STARSolo 2.7.10a, using human genome GRCh38.p12 and transcript annotations from ENSEMBL release 93 from reference package GRCh38-3.0.0 as available from 10Xgenomics, consists of 24 BAM files.

  Dataset EGAD50000001434

• Copy Number Arrays

  Copy Number Alterations arrays from 21 patients and 24 samples performed by Affymetrix 6.0, Agilent 1M and Oncoscan CNV platforms

  Dataset EGAD00010001581

• Dataset of whole-exome sequencing of acute erythroid leukemia

  This dataset includes 48 bam files, including those of 24 tumors and 24 paired normal samples.

  Dataset EGAD00001005074

• H3Africa H3AChipDesign ELSI

  24 samples from Cameroon generated for the H3Africa Chip Design Study. The dataset includes BAM, FASTQ and decompressed gVCF files.

  Dataset EGAD00001004316

• Southern African Human Genome Programme dataset

  The SAHGP characterises the genomes of 24 individuals (8 Coloured and 16 black southeastern Bantu-speakers) using deep whole genome sequencing (WGS).

  Dataset EGAD00001003791

• Whole-genome-seqeuncing IMFT

  Whole-genome sequencing of IMFT tumor samples from 24 participants in the clinical phase II trial EORTC 90101 “CREATE” (CREATE IMFT cohort)

  Dataset EGAD00001007804

• Whole genome sequence of Primary-recurrent HCC study

  This dataset contains whole genome sequence data from 24 samples, including 16 tumors and 8 normal samples. All the experiments were performed on Illumina HiSeq 2000 platform with raw reads stored in fastq format.

  Dataset EGAD00001005451

• Characterization of Arabian Peninsula whole exomes

  We conducted whole exome sequencing (using the SureSelect Human All Exon V5 + UTRs target enrichment kit) of 90 individuals from AP (23 from Saudi Arabia, 24 from Yemen, 24 from Oman and 19 from UAE).

  Dataset EGAD00001009162

• Genome-wide array and mtDNA data Mercheros

  This dataset includes genome-wide autosomal array data and whole mtDNA sequences for 24 Merchero individuals.

  Dataset EGAD00001007763

• Whole-exome sequencing of IMFT tumor samples f

  Whole-exome sequencing of IMFT tumor samples from 24 participants in the clinical phase II trial EORTC 90101 “CREATE” (CREATE IMFT cohort)

  Dataset EGAD00001007803

• Exome sequencing of Non-syndromic Congenital Heart Defects (2019-04-24)

  Exome sequencing of ~1,800 patients with non-syndromic Congenical Heart Defects (CHD) to identify genes enriched for damaging rare variants that increase risk of CHD . This dataset contains all the data available for this study on 2019-04-24.

  Dataset EGAD00001004972

• Exome sequencing of Non-syndromic Congenital Heart Defects (2019-04-24)

  Exome sequencing of ~1,800 patients with non-syndromic Congenical Heart Defects (CHD) to identify genes enriched for damaging rare variants that increase risk of CHD . This dataset contains all the data available for this study on 2019-04-24.

  Dataset EGAD00001004975

• Pre-treatment PD-L1 staining on tumor samples (n=24)

  Data from NABUCCO cohort 1 (NCT03387761). This dataset includes the pre-treatment PD-L1 staining on tumor samples (n=24). Details about the PD-L1 staining can be found on the paper (https://doi.org/10.1038/s41591-020-1085-z)

  Dataset EGAD00001006856

• Gene expression in LPS-stimulated human monocyte-derived macrophages

  This dataset consists of RNA-seq data from human monocyte-derived macrophages that were subjected to siRNA treatment targeting RAD21 and either left untreated, or stimulated with LPS. In total, it includes 24 samples.

  Dataset EGAD00001007952

• 15 Healthy controls, 25 conlonrectal cancer patients without liver metastasis and 24 conlonrectal cancer patients with liver metastasis (target capture)

  15 Healthy controls, 25 conlonrectal cancer patients without liver metastasis and 24 conlonrectal cancer patients with liver metastasis (target capture)

  Dataset EGAD00001009838

• Metastatic breast cancer targeted gene screen (2014-09-24)

  The samples will be sequenced for a targeted panel of cancer relevant genes (n ~ 370) and analysed for somatic mutations. This dataset contains all the data available for this study on 2014-09-24

  Dataset EGAD00001001018

• 24 Chordoma samples (WES,WGS)

  Case series of the rare tumor entity chordoma. 9 cases sequenced with Whole Exome Sequencing (WES) and 2 cases sequenced with Whole Genome Sequencing (WGS) were recruited from the personalized oncology program NCT-MASTER/DKTK-MASTER at the German Cancer Research Center. One of the WES patients was re-sequenced at a later time point when he relapsed, this resequencing was done by WGS. Therefore there are 11 patients, one of which with two samples, all of which were sequenced with matched normal controls, amounting to a total number of 24 NGS samples.

  Dataset EGAD00001004825

• RNA sequencing data to study therapeutic targeting of ependymoma

  This dataset conatains RNA sequencing data from 24 patients. Up to two lanes per tumour sample have been seqeunced on a Illumina HiSeq2000 instrument in paired-end mode resulting in 58 Fastq files.

  Dataset EGAD00001003966