23083 results for "ega"

in 33.18 milliseconds.

• A_cell_atlas_of_the_human_fetal_spine_SB_HDBR_Project_200532

  A cell atlas of the human fetal spine

  Study EGAS00001005090

• SF11310

  Oligodendroglioma, IDH-mutant, 1p19q codeleted

  Dataset EGAD00001008301

• Jagged ends of plasma DNA (human)

  Jagged ends of plasma DNA (human)

  Study EGAS00001005562

• Jagged ends of plasma DNA (mouse)

  Jagged ends of plasma DNA (mouse)

  Study EGAS00001005563

• Neutrophils at timepoint 0h

  Neutrophils at timepoint 0h

  Dataset EGAD00001006807

• The genomic landscape of GCs

  whole-genome sequencing of 168 paired GCs.

  Study EGAS00001007355

• Nimblegen SeqCap Custom Panel Sequencing

  Nimblegen SeqCap Custom Panel Sequencing for pNet

  Dataset EGAD00001005494

• Clinical data

  Clinical data including the treatment arm, HER2 status Pre- and Post-NAT.

  Dataset EGAD00001009414

• Nimblegen SeqCap Sequencing

  Nimblegen SeqCap (sequence capture) deep targetted DNA sequencing pNET

  Dataset EGAD00001005489

• Genome Asia VCF files

  Genome Asia VCF files

  Dataset EGAD00001005975

• SF7003

  Oligodendroglioma (WHO gr. 2)

  Dataset EGAD00001008297

• Neutrophils at timepoint 6h

  Neutrophils at timepoint 6h

  Dataset EGAD00001006809

• Cas9-mtDNA samples

  Dataset including 13 sequenced mtDNA genome samples.

  Dataset EGAD00001008717

• Genomic Sequencing of Triple Negative Breast Cancer - Exome data

  Exome data for study EGAS00001008261

  Dataset EGAD00001015687

• Whole exome sequencing

  Whole-exome sequencing

  Dataset EGAD00001008953

• DATA FILES FOR PCGP SJETP WXS

  DATA FILES FOR PCGP SJETP WXS

  Dataset EGAD00001001248

• BiSeqS

  Runs that contain data for the sensitivity and specificity experiments for BiSeqS.

  Dataset EGAD00001003323

• DONSON exome data

  Exome data from patients and parents with DONSON mutations

  Dataset EGAD00001003160

• dataset for BGI bladder cancer project

  dataset for BGI bladder cancer project

  Dataset EGAD00001000758

• TGCT Whole Exome Sequencing data

  TGCT Whole Exome Sequencing data

  Dataset EGAD00001001222

• WGS dataset

  4 WGS bam files for 4 cases with fusion

  Dataset EGAD00001004359

• Clear cell renal cell carcinoma (HIPO-045)

  Exome from EGAS00001001861

  Dataset EGAD00001002166

• Metastatic Prostate Follow Up 2

  Validation/deeper sequencing for metastatic prostate cancer samples

  Dataset EGAD00001000989

• LCNEC study - WES data set

  Whole exome sequencing

  Dataset EGAD00001003815

• PDAC

  ctDNA and protein markers for earlier detection of pancreatic cancers

  Dataset EGAD00001004399

• SF10679

  Oligodendroglioma, Anaplastic (WHO gr. 3

  Dataset EGAD00001008302

• SF10207

  Oligodendroglioma, Anaplastic (WHO gr. 3

  Dataset EGAD00001008298

• PCHiC

  PCHiC

  Dataset EGAD00001002268

• DNA BAM

  DNA BAM files

  Dataset EGAD00001005503

• Human dnase1l3 deficiency-Mouse AAV samples

  Human dnase1l3 deficiency-Mouse AAV samples

  Dataset EGAD00001006215

• SF4454

  Astrocytoma (WHO gr. 2)

  Dataset EGAD00001006318

• HER2-negative primary breast cancers WES

  Temporal HER2-negative breast cancers WES

  Dataset EGAD00001006980

• SF10922

  Astrocytoma, Anaplastic (WHO gr. 3

  Dataset EGAD00001008307

• IBC RNA-seq

  RNA sequencing of IBC patients

  Dataset EGAD00001011649

• AML WGS bam

  WGS bam files for paired diagnostic and remission samples

  Dataset EGAD00001015515

• HCA Organoids | Colon - Cancer, Nanopore Sequencing Data

  Nanopore Sequencing Data

  Dataset EGAD00001015536

• Test dataset: Sequence and variant data from public 1000 Genomes Project

  This is a test dataset derived from public data of the 1000 Genomes Project. Its purpose is not to allow for any inference about cohort data or results, but to aid bioinformaticians in the technical development and testing of tools, as well as data consumers in learning how to access information. This dataset consists of 2508 samples from the 1000 Genomes Project (https://www.nature.com/articles/nature15393). Samples' (e.g. NA18534) data can be accessed through the IGSR portal (e.g. https://www.internationalgenome.org/data-portal/sample/NA18534) or their corresponding folder at the 1000 Genomes' FTP site (e.g. http://ftp.1000genomes.ebi.ac.uk/vol1/ftp/data_collections/1000_genomes_project/data/CHB/NA18534/exome_alignment/). There are several different types of data this dataset encompasses: Variant Calling Format (VCF, or its binary counterparts BCF) files, both joint (e.g. ALL_chr22_20130502_2504Individuals.vcf.gz) and split (HG01775.chrY.vcf.gz); exome sequencing CRAM files (e.g. NA18534.GRCh38DH.exome.cram); whole genome sequencing CRAM/BAM files (e.g. NA19239.cram). Additionally, there are multiple files that were sliced to create shorter files, which allows for a quick download, formated as "{FILE-INFO}__{NUMBER-OF-READS}r__{CHR}.{START-COORDINATE}-{END-COORDINATE}.{FILETYPE}" (e.g. "HG01500.GRCh38DH__90r__3.10000-10500__4.10000-10500.cram"). These files can be downloaded directly through the EGA-download-client PyEGA3 (https://github.com/EGA-archive/ega-download-client).

  Dataset EGAD00001003338

• The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin.

  Study EGAS00001006088

• The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin.

  Study EGAS00001006122

• The evolutionary dynamics of human colorectal cancer using single-gland spatial multi-omic profiling of DNA, RNA and chromatin.

  Study EGAS00001005827

• High Throughput Data_Hematological Malignancies

  Dac EGAC00001000428

• Children's Cancer Therapy Institute DAC

  Dac EGAC00001001828

• DATA ACCESS WITH REGARDS TO EXOME-WIDE ASSOCIATION ANALYSIS OF CORONARY ARTERY DISEASE IN THE KINGDOM OF SAUDI ARABIA POPULATION

  Dac EGAC00001000420

• DAC for high resolution genomic data generated by the Gisselsson Group at the Department of Clinical Genetics, Lund University.

  Dac EGAC00001000534

• Transcriptional and DNA binding profiling of CEBPE in REH acute lymphoblastic leukaemia cells using shRNA RNA-Seq and ChIP-Seq

  Dac EGAC00001000891

• The data access committee for Multimodal Genomic Features Predict Outcome of Immune Checkpoint Blockade in Non-small Cell Lung Cancer

  Dac EGAC00001001331

• Data access committee for white blood cell and cell-free DNA analyses for detection of residual disease in gastric cancer

  Dac EGAC00001001435

• Data Access Commitee for study Fine-Scale Genomic Analyses Of Admixed Individuals Reveal Unrecognized Genetic Ancestry Components In Argentina

  Dac EGAC00001001634

• Access to aligned sequencing data for study "Loss of SNAI2 in prostate cancer correlates with clinical response to androgen deprivation therapy".

  Dac EGAC00001001809

• Novel de novo pathogenic variant in the GNAI1 as a cause of severe disorders of intellectual development with autistic features

  Dac EGAC00001002145