22941 results for "ega"

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• Circulating tumor DNA, pathological and immunologic responses to neoadjuvant nivolumab or nivolumab plus relatlimab and chemoradiotherapy in resectable esophageal/gastroesophageal junction cancer

  Study EGAS00001007299

• Single-cell multi-omics defines the cell-type-specific impact of splicing aberrations in human hematopoietic clonal outgrowths

  Study EGAS00001007402

• LAM-HTGTS dataset

  LAM-HTGTS dataset after DIS3 ASO or Control ASO treatment on human cells under plasmablast differentiation.

  Dataset EGAD50000001242

• PREGO reference panel - 3234 individuals from Western France. Individuals' birthplaces are available in epsg.io/2154 (RGF93 v1 / Lambert-93 -- France) coordinates.

  Study EGAS00001007764

• sc-RNA-Seq soft tissue sarcoma tumoroid biobank

  Dataset EGAD00001009002

• Mechanism of Decitabine response in MDS/AML patients

  Data access agreement for access to scRNASeq data of serial AML/MDS patients undergoing decitabine treatment.

  Dac EGAC50000000550

• UTSW KCP DAC

  This DAC manages access to WES and RNA-Seq data from studies approved under the IRBs of KCP principal investigators.

  Dac EGAC50000000203

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

  WES in 23 Angolan and 7 Cape Verdean triple-negative breast cancer samples

  Dac EGAC50000000486

• Clonotype Analysis Data

  This dataset includes: amplicon sequencing data for a total of 3 BCP-ALL patients - fastq files

  Dataset EGAD50000001518

• BCG prime DNA methylation data

  This dataset contains the DNA methylation data of 384 samples from individuals with one or more comorbidities

  Dataset EGAD00010002767

• Ovarian subtypes tumor methylation data

  This dataset contains ovarian endometriod and ovarian, stomach, pancreatic and colorectal mucinous tumor tissue samples

  Dataset EGAD00010002773

• Exome sequencing for identifying point mutations driving M haemophilum susceptibility

  To understand non tuberculous Mycobacterial susceptibility

  Study EGAS50000001076

• cfDNA shallow Whole-Genome sequencing - healthy donors

  sWGS of the blood samples from 14 (fourteen) healthy donors

  Dataset EGAD50000001860

• SiMSen‑Seq

  High resolution amplicon-bases sequencing o screen for PIK3CA hot spot mutations

  Dataset EGAD50000001668

• DNAme of pancreatic neuroendocrine tumors mutated in MEN1/DAXX/ ATRX

  primary pancreatic neuroendocrine tumors mutated in Menin, DAXX or ATRX

  Dataset EGAD00010002784

• CFTR Gene Variant Detection in Moroccan Individuals via Nanopore Long-Read Sequencing

  This is data from LRS of CFTR gene on CF Moroccan patients

  Dac EGAC50000000815

• endogene.bio

  The Endogene Bio Data Access Committee oversees and manages access to controlled genomic and clinical datasets deposited by the Endogene Bio research team.

  Dac EGAC50000000786

• FFPE_Normal_Panel_V3_Cancer_Panel

  FFPE normal panel generation for use with V3 cancer panel 0618521

  Study EGAS00001000836

• Otosclerosis_gene_discovery_

  DNA from patients with otosclerosis will be subjected to exome sequencing

  Study EGAS00001000156

• SHH medulloblastoma samples

  Sequencing data of human SHH medulloblastoma samples

  Study EGAS00001000607

• Breast_Heterogeneity_Validation

  Validation of subs and indels called in breast whole genome studies

  Study EGAS00001001972

• Whole Exome Sequencing of Permanent Neonatal Diabetes Patients

  Whole Exome Sequencing of Permanent Neonatal Diabetes Patients

  Study EGAS00001000047

• Cloning_of_the_breakpoint_of_a_novel_translocation_associated_with_T_acute_lymphoblastic_leukaemia

  Single case of T-ALL carrying t(4;6), a novel translocation.

  Study EGAS00001000520

• ICR MOPOPGEN UK exome control series

  BAM files of individuals from the 1958BC aligned to hg17

  Dataset EGAD00001004396

• HipSci - Embryonic Stem Cells - Exome Sequencing - April 2016

  HipSci - Embryonic Stem Cells - Exome Sequencing - April 2016

  Dataset EGAD00001001999

• Reference epigenome OB56_N_PreA_WGBS data generated from KEP study

  A OB56_N_PreA_WGBS paired end data for Preadipocytes(fat)

  Dataset EGAD00001003479

• IRF5 HL RNASeq dataset

  bam files associated with the study EGAS00001001205

  Dataset EGAD00001001417

• Pipeline study - RNAseq dataset

  Fernandez-Cuesta et al., RNAseq data Pipline

  Dataset EGAD00001000746

• DREAM SMC-HET - WGS mapped reads

  ICGC-TCGA DREAM Somatic Mutation Calling - Tumour Heterogeneity Challenge - WGS mapped reads

  Dataset EGAD00001003971

• Landscape of AL mutations

  Exome Sequencing to Define the Landscape of Plasma Cells in Systemic Light chain Amyloidosis

  Dataset EGAD00001001861

• Illumina_WXS_CONT

  Whole-exome sequencing on Illumina HiSeq2000/2500 of normal colon control tissue

  Dataset EGAD00001002094

• WGS of Asian lung cancers

  VCF files of somatic variants from tumor-normal pairs of Asian lung cancer patients

  Dataset EGAD00001001240

• OT2_Illumina_WGS_BL

  Whole-genome sequencing on Illumina HiSeq2000/2500 of Blood EDTA (OT2_cohort)

  Dataset EGAD00001003370

• Oxford Nanopore sequencing for APL

  Raw fast5 file of Oxford Nanopore sequencing for an APL patient sample

  Dataset EGAD00001008151

• MDS 5q- exome reads

  Cancer exome reads consisting of FASTQ paired end reads from bone marrow samples

  Dataset EGAD00001001058

• Microsatellite unstable colorectal cancers

  Mapped data for 10 Colon MSI cancer samples

  Dataset EGAD00001004500

• MDS Sequential Treatment Validation

  Validations of variants identified by exome sequencing in sequential samples derived after treatment cycle with AZA.

  Dataset EGAD00001000949

• IMpower133 subtype assignments

  This dataset contains subtype assignments for 271 tumor samples profiled by RNA-seq.

  Dataset EGAD00001006926

• Solid_WXS_BL

  Whole-exome sequencing on AB 5500xl Genetic Analyzer of Blood EDTA

  Dataset EGAD00001002104

• Disorders of growth and insulin action

  Illumina paired-end sequencing of whole- exome pulldown DNA from Severe Insulin Resistant patients.

  Dataset EGAD00001000381

• Target sequencing of myxofibrosarcoma

  Target sequencing (fastq files) of 99 pairs (198 samples) of myxofibrosarcoma

  Dataset EGAD00001004101

• AI_NF1glioma_WES

  The dataset includes 59 tumor samples from 56 NF1-glioma patients profiled by Whole Exome Sequencing.

  Dataset EGAD00001004375

• Tracing the origins of relapse in AML to stem cells

  Aligned whole genome sequence from AML relapse project

  Dataset EGAD00001003234

• snv calls for subclonal reconstruction

  single nucleotide variant calls from somatic sniper, vcf format. input for subclonal reconstruction

  Dataset EGAD00001003753

• RNA sequencing of myxofibrosarcoma

  RNA sequencing (fastq files) of 29 samples of myxofibrosarcoma

  Dataset EGAD00001004102

• Exome sequencing Parkinson's disease patients

  In this project we will sequence the exomes of 250 patients with Parkinson's disease

  Dataset EGAD00001000405

• Targeted gene screen of drug resistant organoids

  Sequencing of drug resistant organoids

  Dataset EGAD00001003252

• Multisample2 Amplicon

  Amplicon data of tumor samples generated for validation of WES findings and further sub clonal mapping

  Dataset EGAD00001004020

• Familial CEBPA-mutated AML whole exome sequencing dataset

  Whole exome sequencing data for AML and matched normal samples

  Dataset EGAD00001000996

• Whole exome sequencing of myxofibrosarcoma

  Whole exome sequencing (fastq files) of 41 pairs (82 samples) of myxofibrosarcoma

  Dataset EGAD00001004095