23155 results for "ega"

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• Massachusetts General Hospital Cancer Center DAC for high-throughput microfluidic enrichment from whole leukopak for CTC-based liquid biopsy

  Whole genome sequencing and whole exome sequencing data of circulating tumor cells isolated from patients with metastatic prostate cancer and liver cancer.

  Dac EGAC50000000423

• Whole genome sequencing profiling of patient-derived organoids (PDO)

  Whole genome sequencing profiling of 41 PDAC patient-derived organoids (PDO) - WGS unmapped reads, sequenced using NovaSeq 6000, 15x coverage 160 million reads per sample.

  Dataset EGAD50000000280

• Transcriptomics for the ALTTO study

  Transcriptomics for the ALTTO study by high-throughput sequencing. 386 HER2+ breast cancers treated by trastuzumab were sequenced. Two fastq files are given for each sample.

  Dataset EGAD50000000746

• scRNA data of multiple myeloma

  Dataset containing 36 samples of multiple myeloma. The sequencing was always paired and performed on Illumina NextSeq 550 and Illumina NovaSeq 6000.

  Dataset EGAD50000000438

• scRNAseq data from metastatic breast cancer samples

  Paired-end SMARTseq2 data of EpCAM+ sorted cells from liquid biopsies from 3 patients. Sequencing was performed on Illumina HiSeq 2500.

  Dataset EGAD50000000816

• CARE iSGS single nucleus RNA-seq

  This study contains single nucleus RNA-sequencing data from healthy controls, iSGS, and traumatic subglottic stenosis patients.

  Study EGAS50000000878

• ATAC-seq samples from 9 cHL cell lines

  The dataset contains 21 ATAC-seq samples from 9 cHL cell lines. Files within the dataset are raw fastq files for each cell line.

  Dataset EGAD50000001273

• Cell targeted amplification sequencing (cta-seq) of scRNA-seq sample

  This data-set contains two sequencing runs of the same scRNA-seq library. Once with and once without cell targeted amplification of transcripts.

  Dataset EGAD50000001338

• CIRCLE-seq of PDAC PDO

  CIRCLE-seq was performed on a PDAC PDO to validate the presence and the structure of ecDNAs

  Study EGAS50000000194

• N2M2 methylation array data

  Methylation profiling of 228 samples, using the approach described in "Molecularly matched targeted therapies plus radiotherapy in patients with newly diagnosed glioblastoma without MGMT promoter hypermethylation (N2M2/NOA-20 phase I/IIa umbrella trial)"

  Dataset EGAD00010002747

• Human Heredity and Health in Africa Data Access Committee

  Dac EGAC00001000648

• IGV gene profiling of IGH+ and IGHUND HGBCL-DH-BCL2(-BCL6),revealed by NGS of 5'RACE PCR products

  NGS of 5'RACE IGKV/IGLV PCR-products from IGH+ and IGHUND HGBCL-DH-BCL2(-BCL6) lymphomas

  Dataset EGAD50000001526

• Whole genome sequencing of metachronous FL-High-Grade-B-Cell-Lymphomas, classified according to IGH status

  FL-HGBCL-DH-BCL2(-BCL6) metachronous lymphoma pairs, classified according to IGH status in IGH+ or IGH-undetectable

  Dataset EGAD50000001528

• WES in Angolan and Cape Verdean triple-negative breast cancer samples

  WES (using the SureSelect Human All Exon V5 + UTRs target enrichment kit) in 23 Angolan and 7 Cape Verdean triple-negative breast cancer samples

  Dataset EGAD50000001482

• Short-read mRNA sequencing of human normal liver organoid with or without SF3B4 overexpression

  Project aims to find alternative splicing events and resulting transcript isoforms modulated by SF3B4

  Study EGAS50000000851

• p200503_fn2

  RNA-Sequencing data of Fusobacterium nucleatum (Fna 71) treated CRC patient derived (CAF180, CAF181) and CAF05 cancer associated fibroblasts (CAFs).

  Study EGAS50000001121

• Evaluation of the ERa binding region activity in breast and endometrial cancer

  Evaluate the activity of ERa binding site activity in breast and endometrial cancer.

  Study EGAS50000000009

• Akershus University Hospital Data Access Committee for Immunoglobulin Heavy-Chain locus in Multiple Sclerosis datasets in FEGA Norway

  This is the Data Access Committee appointed by Akershus University Hospital (AHUS) for datasets from Immunoglobulin Heavy-Chain locus in Multiple Sclerosis studies.

  Dac EGAC50000000659

• RNA Sequencing of Control and Myotonic Dystrophy Type 1 Cells During Myogenic Differentiation

  RNAseq data of 30 muscle cell samples (proliferating myoblasts to differentiating myotubes) of immortalized control cells, and myotonic dystrophy type 1 (DM1) patient-derived cells and their edited versions.

  Dac EGAC50000000592

• MD Anderson Cancer Center HGSOC LRS Data Access Comittee

  Oxford Nanopore long-read sequencing was performed on six paired tumor-normal samples from patients with high-grade serous ovarian carcinoma. Reads were mapped to the GRCh38 reference genome, incorporating base modification information.

  Dac EGAC50000000597

• Primary human hepatocyte ATAC-seq

  Profiling the chromatin accessibility landscape of cultured primary human hepatocytes (PHH) from three female and three male adult, non-diabetic donors.

  Dataset EGAD50000001751

• DCC_R26.PRAD-CNSM-Array

  Raw Array data from the PRAD-CA for ICGC DCC Release26

  Dataset EGAD00010001414

• WES-based association study of cefaclor-induced anaphylaxis

  This study investigates the genetic factors associated with cefaclor-induced anaphylaxis using whole-exome sequencing (WES).

  Study EGAS50000001163

• Delineating pediatric brain tumor progression using single-nuclei sequencing

  raw fastq files from the single-nuclei RNA-seq experiments generated from 42 paediatric CNS tumour samples by the 10X Genomics technology.

  Dataset EGAD50000001831

• Maternally-Inherited SPTBN1 Mutation

  The dataset consists of exome sequencing data from a male patient with a maternally inherited SPTBN1 mutation. The clinical presentations include autism spectrum disorder, cognitive delay, feeding difficulties, gastrointestinal manifestations, and musculoskeletal abnormalities.

  Dataset EGAD50000001726

• Single-cell RNA-seq from tumor-on-chip (TOC)

  8 Fastq files of single-cell RNAseq data from tumor-on-chip (TOC) after 42h of TNBC and CAF mono- or co-culture

  Dataset EGAD50000001296

• B-cell precursor acute lymphoblastic leukemia acute lymphoblastic leukemia Micro-C sequencing data Data Access Committee

  This dataset included 33 childhood B-cell precursor (BCP) acute lymphoblastic leukemia Micro-C samples. All samples were subjected to Illumina pair-end sequencing.

  Dac EGAC50000000467

• WES_dataset1

  Fourteen MEITLs and one EATL previously had been sequenced using the SureSelectXT Target Enrichment System (Agilent Technologies, Santa Clara, CA, USA).

  Dataset EGAD50000001620

• LBC1921 gvcfs

  297 members of the LBC1921 were sequenced using the Illumina HiSeq X platform. This dataset contains the gvcfs.

  Dataset EGAD00001006416

• scRNA-seq for 4 reactive lymph node and 12 high grade B cell lymphoma samples

  Dataset includes count matrices, barcode tsvs, and features tsv for each sample, generated using Cell Ranger.

  Dataset EGAD50000001386

• β-catenin ChIP sequencing in HCC models.

  This dataset contains ChIP sequencing data for β-catenin, H3K27ac and H3K27me3 from three HCC cell lines and five tumour organoids under normal conditions and oleic acid treatment.

  Dataset EGAD50000001816

• Variant calling for UPST-SCCHN3 cohort

  Tumor versus Germline variant calling on UPST-SCCHN3 cohort

  Dataset EGAD50000002178

• DDD Phenotype Dataset

  Phenotype data for 1230 participants from both South Africa and The Democratic Republic of Congo

  Dataset EGAD00001015752

• Pineoblastoma Single-Nuclei RNA-seq Data Access Committee (St. Jude)

  Committee responsible for reviewing and approving external access requests to controlled-access pediatric brain tumor transcriptomic datasets from St. Jude Children's Research Hospital, ensuring alignment with patient consent and institutional ethics policies.

  Dac EGAC50000000839

• DAC for lymphoma IFZ Essen

  This DAC is set in place to handle acess to data on lymphomas and immune cells submitted by scientists from the Institute of Cell Biology (Cancer Research) at the University of Duisburg-Essen in Essen, Germany.

  Dac EGAC50000000521

• Long read whole genome sequencing data from brain postmortem tissue

  Chart genetic variation in the human brain in healthy controls and Parkinson’s disease (PD) patients.

  Study EGAS50000000921

• ONT and PacBio data of 22q11 patient-parent duos/trios

  ONT and PacBio FASTQ files generated for de novo assembly and resulting de novo assemblies

  Study EGAS50000001647

• DAC Dr MAMI-CHOUAIB

  Principal Investigator Dr Fathia MAMI-CHOUAIB (Fathia.Mami-Chouaib@gustaveroussy.fr) Researcher Dr Stephanie CORGNAC (Stephanie.CORGNAC@gustaveroussy.fr) Head of Bioinformatics platform Dr Marc Deloger (Marc.DELOGER@gustaveroussy.fr) Data Manager Dr Aziza CAIDI (Aziza.CAIDI@gustaveroussy.fr) Data Protection Officer Clara BECHET (Clara.BECHET@gustaveroussy.fr)

  Dac EGAC50000000511

• Targeted capture sequencing for LySeqST

  Targeted capture sequencing of 445 lymphoma samples and 13 normal samples for LySeqST: A targeted sequencing assay for robust genomic classification of diffuse large B-cell lymphoma.

  Dataset EGAD50000002290

• Genome-wide genotyping and methylation data from Understanding Society

  Genome-wide genotyping and methylation data from Understanding Society. Please visit https://www.understandingsociety.ac.uk/ for further information.

  Study EGAS00001008417

• irCLIP library generated from HEK293 cells overexpressing 3FLAG-RIG-I gain-of-function variant C268F

  irCLIP library generated from HEK293 cells transfected with either RIG-IWT or RIG-IC268F (n=3).

  Dataset EGAD50000002390

• Dataset for whole exome sequencing of PTCLs

  The dataset consists of whole exome sequencing FASTQ files and analyzed data, including single nucleotide variants (SNVs) and short insertions and deletions (Indels) of candidate driver genes.

  Dataset EGAD50000001798

• De novo metastatic prostate cancer cohort

  Fastq files from RNA sequencing of normal and tumor samples from 16 patients from the de novo metastatic prostate cancer cohort.

  Dataset EGAD50000002381

• Triple-negative breast cancer - Visium HD data

  Visium HD aligned reads from patient 1D525, BAM file from 10X spaceranger output directory

  Dataset EGAD50000002284

• Pancreatic Cancer Sequencing Initiative

  Pancreatic Cancer Sequencing Initiative for the International Cancer Genome Consortium at the Ontario Institute for Cancer Research.

  Study EGAS00001000343

• Copy Number Variation using Affymetrix Optima Array

  Diagnostic yield of affymetrix optima microarray in patients with non-syndromic autism spectrum disorders in India.

  Study EGAS00001006439

• Myeloproliferative_Neoplasms__MPN__Exome_Validation_Study

  Experiments using targeted pulldown methods will be sequenced to validate findings in the exomes of patients with Myeloproliferative Neoplasms (MPN).

  Study EGAS00001000404

• Colorectal_organoids_and_tumour_tissue

  Whole genome sequencing of single cell derived organoids from normal colon tissue and colorectal cancer.

  Study EGAS00001000881

• ESGI___Whole_Genome_Sequencing_of_NSPHS_samples

  Whole genome sequencing of sampels from the NSPHS cohort. The samples are sequenced using the Illumina HiSeq X Ten system.

  Study EGAS00001001117

• Exome and RNA sequencing of Greenlanders

  This study contains whole exome sequence of 27 Greenlanders and deep RNA sequencing of 17 Greenlanders

  Study EGAS00001002727