23085 results for "ega"

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• oacoch-M-1

  Methylation changes in OA patients with chronic exposure to cobalt and chromium

  Dataset EGAD00010001040

• DNA Methylation profiles of colorectal cancer samples

  Illumina 450K DNA methylation profiles of 314 fresh-frozen colorectal mucosa, adenoma or adenocarcinoma samples.

  Dataset EGAD00010001888

• Proteom study primary CRC and LM

  Proteom characterization in primary colorectal cancer and corresponding liver metastasis

  Dataset EGAD00010002237

• CIRdb-CEU1

  Single Nucleotide Polymorphisms in autosomes of Canary Islanders

  Dataset EGAD00010002294

• Serum Proteomics of Aortic Diseases

  Comparative proteome-based analysis of different autologous bone entities used for alveolar onlay grafting

  Dataset EGAD00010002314

• OSC HumanCoreExome Genotypes

  DNA was extracted from saliva samples and genotyping was performed on Illumina Infinium HumanCoreExome beadchips.

  Dataset EGAD00010002375

• PDAC organoid genomic heterogeneity

  Two primary tumor-derived PDAC organoids were subjected to SNP array, RNA-seq, and single-cell WGS

  Dataset EGAD00010002408

• Transcriptome of (peripheral blood), from donor Sample A, replicate 1 FACS processing technical replicates

  FACS processing technical replicates

  Dataset EGAD00001010086

• nwa.data.IF.papers

  Genome-wide SNP from 221 individuals from Northwestern Amazonia genotyped on the Affymetrix Human Origins Array

  Dataset EGAD00010002394

• Transcriptome of (peripheral blood), from donor Sample A, replicate 2 FACS processing technical replicates

  FACS processing technical replicates

  Dataset EGAD00001010087

• UM

  metabolite levels provided by UM platform (Creative Dynamics Inc, NY, USA) (the data is raw abundance. Mapping was applied on log10 transformed data)

  Dataset EGAD00010002146

• SNParray_PGT_samples_scGBS

  PGT samples for haplotyping and copy-number profiling via SNP array

  Dataset EGAD00010002169

• SNParray_HapMap_samples_scGBS

  HapMap samples for haplotyping and copy-number profiling via SNP array

  Dataset EGAD00010002168

• Knoll et al Identification of drug candidates targeting monocyte reprogramming in people living with HIV

  Bulk RNAseq PBMC

  Dataset EGAD50000000068

• Bulk tumor RNASeq RPMK files from 65 patients

  Bulk tumor RNASeq RPKM files from 65 patients.

  Dataset EGAD50000000126

• scRNAseq data of HGSOC patients before and after treatment

  scRNAseq data of HGSOC patients before and after treatment

  Dataset EGAD50000000191

• Granulosa cell tumor

  Genome-wide NanoRCS of cfDNA from plasma of Granulosa cell tumor patients

  Dataset EGAD50000000218

• Multiregion exome sequencing of ovarian immature teratomas

  Clinicopathologic features of the ten patients with ovarian immature teratomas studied by whole-exome sequencing

  Dataset EGAD50000000421

• scRaCH-seq data targeting BTK and SF3B1

  Data set for scRaCH-seq manuscript. We base call the fast5 using guppy.

  Dataset EGAD50000000235

• Single-Cell RNA-seq of Primary High Grade Serous Carcinoma

  Single-cell RNA Sequencing of CD45- cancer cells.

  Study EGAS50000000068

• HMO-microbiome study dataset, 16S sequencing

  This dataset contains 16S sequencing of fecal and milk samples for HMO-microbiome Lifelines NEXT study

  Dataset EGAD50000000532

• cfRRBS data plasma healthy donor

  cfRRBS data produced from the cfDNA in plasma isolated from healthy, adult donors.

  Dataset EGAD50000000553

• H3K27ac ChIP-seq in Insulinomas

  H3K27ac ChIP-seq datasets in human insulinoma samples

  Dataset EGAD50000000461

• Cancer Genomics, ICR, summary data

  DAC for summary level data from the Cancer Genomics group, Division of Genetics and Epidemiology at the Institute of Cancer Research, Sutton, UK.

  Dac EGAC50000000050

• Center of Medical Genetics Ghent - lab BMN

  This is a DAC created to contain datasets generated in lab BMN, part of the Center of Medical Genetics Ghent, Belgium.

  Dac EGAC50000000351

• H3Africa KDRN Genotype

  The 6431 samples were genotyped on the H3Africa array.

  Dataset EGAD00010002365

• Targeted nanopore sequencing of MARCHF6 repeat expansions

  This dataset includes FASTQ files from MARCHF6 alleles sequenced by targeted nanopore in 8 patients.

  Dataset EGAD50000000812

• Exonic Counts

  Read counts, per gene, aligning to exons. Alignment performed with GSNAP. 20 samples.

  Dataset EGAD50000000820

• PDiamond Korean Lung Cancer Data

  WES and RNA-seq data of PDiamond Korean lung cancer data

  Dataset EGAD50000000844

• Foundation Medicine Binary Calls

  Binary calls for all available samples in 4 Atezo trials.

  Dataset EGAD50000000709

• Whole Exome Sequencing data from Neodurvarib Clinical Trial

  Sequencing data related to the genomic profiling of advanced urotelial carcinomas, including tissues from pre and postneoadyuvancy (Olaparib and Durvalumab)

  Dac EGAC50000000471

• Picuris Pueblo Genomic Project (Modern Data)

  Data Access Committee for the present-day dataset of the project "Picuris Pueblo oral history and genomics reveal continuity in US Southwest".

  Dac EGAC50000000526

• Neurodevelopment_Nantes_hospital

  The neurodevelopmental team in the genetics unit of Nantes hospital focus on the identification on new genes causing neurodevelopmental disorders through whole-genome and transcriptomics sequencing.

  Dac EGAC50000000542

• DNABR

  Genome variation data for 2723 Brazilian individuals from the DNA do Brasil Project.

  Dataset EGAD50000001012

• Single-cell multiomics reveals the interplay of clonal evolution and cellular plasticity in hepatoblastoma

  Dataset EGAD00001010049

• WGS data from MTB-Guided Targeted Treatments paper

  WGS data from biliary tract cancer samples (Beaudry et al, 2025; n=55)

  Dataset EGAD50000001418

• DAC for DRS peripheral blood, University Medical Center Johannes Gutenberg University Mainz

  This DAC is in relation to the DRS samples of peripheral blood of healthy control

  Dac EGAC50000000667

• WGSPD Project 3 UCLA DAC

  Data Access Committee to review applications to access Whole Genome Sequencing in Psychiatric Disorders (WGSPD) Project 3 data (WGS) from Dutch cohorts.

  Dac EGAC50000000442

• TRACERx NSCLC - Whole exome multiregion sequencing data

  Study EGAS00001006494

• University Clinic Golnik DAC

  DAC of the University Clinic Golnik, that will decide regarding the requests for data submitted on behalf of research groups of the Clinic

  Dac EGAC50000000820

• WES of bladder tumors from 24 patients

  This dataset contains 144 files fastq files sequenced with Illumina HiSeqX.

  Dataset EGAD50000001775

• WGS_TALL_t_14_16_translocation

  WGS data for patients with t(14;16) translocated T-ALL.

  Dataset EGAD50000001782

• NANOPORE_TALL_t_14_16_translocation

  Nanopore sequencing for patients with t(14;16) translocated T-ALL

  Dataset EGAD50000001785

• U12 Spliceosome Defect Data Access Committee

  This Data Access Committee controls access to data pertaining to the study of the minor spliceosome and it's role in monogenic diabetes.

  Dac EGAC50000000892

• RNAseq of fibroblasts

  RNA sequencing data of fibroblasts from 3 controls and 3 patients with RBMX variants.

  Dataset EGAD50000002371

• Dnase1l3 knockout causes aberrations in plasma DNA fragmentation

  Dnase1l3 knockout causes aberrations in plasma DNA fragmentation

  Study EGAS00001003174

• Wilm's tumor sequencing data

  This study shares DNA and RNA sequencing data from Wilm's tumor patients

  Study EGAS00001005690

• HCA_Skin_Disease_WSSS_Spatial_NCL

  Defining the spatial transcriptome and cell-cell interactions in eczema and psoriasis skin

  Study EGAS00001005278

• Brain_Disease_Wellcome_Leap_Delta_Tissue_Spatial

  Utilising Spatial Transcriptomics to investigate how the tumour microenvironment regulates glioblastoma cell states.

  Study EGAS00001005801

• Gene_Discovery_in_Age_Related_Hearing_Loss

  The aim is to find new candidate genes associated with progressive hearing loss

  Study EGAS00001000295