-
Total RNAseq in the sporadic ALS and healthy control motor cortex
Study
EGAS00001004286
-
Renal_Follow_Up_Series
Study
EGAS00001000095
-
Microenvironment subtypes and association with tumor cell mutations and antigen expression in follicular lymphoma
Study
EGAS00001006052
-
Germline and somatic variants in myelodysplastic syndrome and therapy-related myeloid neoplasms
Dataset
EGAD00001004861
-
Resuscitation Outcomes Consortium (ROC) Prehospital Resuscitation Using an Impedance Valve and Early Versus Delayed Analysis (PRIMED) (ROC-PRIMED-BioLINCC)
Study
phs003825
-
Evaluation of Hybridization Capture versus Amplicon-based Methods for Whole Exome Sequencing
Study
phs000938
-
BrainCloud: Data from human postmortem brain procurement for the neuropathology section
Study
phs000417
-
NHLBI TOPMed: Novel Risk Factors for the Development of Atrial Fibrillation in Women
Study
phs001040
-
Tandem duplication of chromosomal segments is common in ovarian and breast cancer genomes
Dataset
EGAD00001000050
-
Evaluation of Ancestry Admixture among Chileans
Study
phs001385
-
Renal_habitat_RNA
Study
EGAS00001003704
-
Convergent evolution towards CD38 biallelic loss is a recurrent mechanism of resistance to anti-CD38 antibodies in multiple myeloma.
Study
EGAS50000000709
-
Transcriptomic profiles of early and late passage metastatic colorectal cancer (mCRC) tumoroids
Study
EGAS50000000108
-
Genetics of diffuse large B-cell lymphoma in Japan
Study
JGAS000307
-
Deregulation of DUX4 and ERG in acute lymphoblastic leukemia
Study
EGAS00001001923
-
Genome-Wide Association Study of Hypertriglyceridemia in Mexicans
Study
phs000618
-
HLA-DR is absent in primitive macrophages through epigenetic silencing of master regulator CIITA
Study
EGAS00001006981
-
Optimizing Primary Stroke Prevention in Children with Sickle Cell Anemia (STOP II)
Study
phs002386
-
Heart Failure Network Oral Iron Repletion Effects on Oxygen Uptake in Heart Failure (HFN IRONOUT-BioLINCC)
Study
phs003557
-
Pediatric Papillary Thyroid Carcinoma RNA-Seq
Study
EGAS00001005182
-
Acute Respiratory Distress Network (ARDSNet) Study 04 Assessment of Low Tidal Volume and Elevated End-Expiratory Volume to Obviate Lung Injury (ALVEOLI-BioLINCC)
Study
phs003714
-
AVENIO Expanded ctDNA panel sequence alignments (BAMs)
Dataset
EGAD50000000138
-
Admixture histories of São Tomé e Príncipe.
Dataset
EGAD50000001348
-
Single-cell RNA-Seq analysis of thymic ILC1 progenitors and NK cell differentiation This analysis involved a multiplexed sequencing run to study thymic innate lymphoid cells (ILCs) and NK progenitors. The generated data requires a demultiplexing file to separate and identify the individual sample tags for downstream analysis.
Dataset
EGAD50000001157
-
10X single cell sequencing of HNT34 cocultured with Tcells with or without antibody targeting SLAMF6
Dataset
EGAD50000001573
-
Variant calling for IMMU-SCCHN1 cohort
Dataset
EGAD50000002205
-
Neo-RT sWGS
Dataset
EGAD50000002238
-
Exome Sequencing to Identify Causes of Leukaemia Predisposing Congenital Neutropenias (2019-08-19)
Dataset
EGAD00001005264
-
Clinical and biomarker dataset
Dataset
EGAD00001009797
-
SOFT study - sequencing premenopausal breast cancer (2017-11-22)
Dataset
EGAD00001003811
-
Congenital anosmia 1
Dataset
EGAD00001002210
-
Genomic and transcriptomic determinants of therapy resistance and immune landscape evolution during anti-EGFR treatment in colorectal cancer
Dataset
EGAD00001004501
-
Longitudinal Study of Fluoride and Other Factors Related to Dental Fluorosis, Dental Caries, and Bone Health
Study
phs002203
-
Study on the Genetics of Alcoholism (COGA): Smoke Screen and Exome Sequencing
Study
phs001208
-
Differential Presence of Exons in Cell-Free DNA Reveals Different Patterns in Colorectal Cancer Between Metastatic and Non-Metastatic Patients
Study
EGAS00001002687
-
COLO-829/COLO-829BL
Dataset
EGAD00000000055
-
UNC Tumor Donation Program Set 2021
Study
phs002429
-
Genetic Epidemiology Network of Arteriopathy (GENOA)
Study
phs000379
-
ctDNA to predict risk of progression and death after trifluridin/tipiracil therapy
Study
EGAS00001006883
-
A Population Genomics Study Using a Disease-Targeted Cell model: Integration of
Study
phs000225
-
Newborn Screening Translational Research Network (NBSTRN): Newborn Sequencing in Genomic Medicine and Public Health (NSIGHT2)
Study
phs002094
-
Sudden Death in the Young Case Registry
Study
phs003221
-
Genomics of Substance Use Disorders in Latin American Populations
Study
phs003558
-
Germline Genomic Analyses of Breast Cancer in Latinas
Study
phs003144
-
Dana-Farber Cancer Institute (DFCI) Brown Lab CLL Sequencing Study
Study
phs000879
-
CLDN14 mutation identifed from Japanese sensorineural hearing loss patient.
Study
JGAS000191
-
Spontaneous mutations in the single TTN gene represent high tumor mutation burden
Study
EGAS00001004009
-
First genome-wide association study in an Australian Aboriginal population provides insights into genetic risk factors for Body Mass Index and Type 2 Diabetes
Study
EGAS00001001004
-
Indexing Genes Impacted by Copy Number Variation in Developmental Disorders
Study
phs001154
-
NIAID Centralized Sequencing Program
Study
phs001899