-
Whole Genome Sequencing of Bilateral Cleft Lip and Palate Families from Africa: CIDR
Study
phs002623
-
Kids First: Whole Genome Sequencing Studies of Multiplex Nonsyndromic Cleft Lip/Palate Families
Study
phs002626
-
Discovering the Genetic Basis of Cleft Palate: CIDR
Study
phs002220
-
Center for Craniofacial and Dental Genetics (CCDG): Genetics of Orofacial Clefts, Sub-types, and Subclinical Phenotypes - CIDR
Study
phs002815
-
Genetic Analysis of Syndromic Orofacial Clefting
Study
phs002997
-
Center for Craniofacial and Dental Genetics (CCDG): Genetics of Orofacial Clefts and Related Phenotypes
Study
phs000774
-
Kids First: Genomic Studies of Orofacial Cleft Birth Defects
Study
phs001168
-
Gene mutation and rescue in congenital diaphragmatic hernia
Study
phs000485
-
International Consortium to Identify Genes and Interactions Controlling Oral Clefts
Study
phs000094
-
Kids First: Genomics of Orofacial Cleft Birth Defects in Latin American Families
Study
phs001420
-
NIMH (National Institute of Mental Health) De Novo Mutation Identification in Taiwanese Schizophrenia Trios
Study
phs001196
-
Targeted Sequencing of GWAS Loci in Cleft Lip and Palate
Study
phs000625
-
Whole exome sequencing in multiplex cleft families from a consortium
Study
phs000459
-
The epigenetic landscape controlled by p63 in epidermal development
Study
phs001737
-
Center for Craniofacial and Dental Genetics: Study of Dental Caries and Cleft Lip/Palate in Guatemala
Study
phs000440
-
Genome-wide Association Study for Non-syndromic Clefts in the African Population: CIDR
Study
phs001090
-
Center for Craniofacial and Dental Genetics: Exome Sequencing of Orofacial Cleft Families
Study
phs001675
-
Genome-wide NanoRCS of cfDNA from plasma of healthy individuals
Study
EGAS50000000695
-
Genetic Modifiers of Syndromic Orofacial Clefts
Study
phs002221
-
Single Duplex DNA Sequencing with CODEC Detects Mutations with High Sensitivity
Study
phs003255
-
Pre-existing immunity drives the response to neoadjuvant chemotherapy in esophageal adenocarcinoma
Study
EGAS00001007245
-
Genome-wide NanoRCS sequencing of cfDNA and ctDNA from liquid biopsies of healthy individuals and cancer patients
Study
EGAS50000000154
-
Local In Time Statistics for processual research
Study
EGAS00001002520
-
The Genomic Landscape of Interval Colorectal Cancers
Study
phs003093
-
Homozygous Duplication Identified by Whole Genome Sequencing Causes LRBA Deficiency
Study
phs002557
-
Kids First: Genomics of Orofacial Clefts in the Philippines
Study
phs002595
-
Exome sequencing of familial high-grade serous ovarian carcinoma reveals heterogeneity for rare candidate susceptibility genes
Study
EGAS00001004235
-
CCND1-negative MCL
Study
EGAS00001003060
-
GWAS Results from Danjou et al, Nature Genetics 2015
Study
EGAS00001003645
-
Detection of cancers three years prior to diagnosis using plasma cell-free DNA
Study
EGAS00001008068
-
Genome analysis of oesophageal cancer and Barrett's oesophagus
Study
EGAS00001002864
-
Illumina HumanCoreExome genotyping data from the British Society for Surgery of the Hand Genetics of Dupuytren’s Disease consortium (BSSH-GODD consortium) collection
Study
EGAS00001001206
-
Ribosome profiling shows variable sensitivity to detect open reading frames for conventional and different types of cryptic T cell antigens
Study
EGAS50000000322
-
Rapid Whole Genome Sequencing for Genetic Disease Diagnosis in Neonatal Intensive Care Units
Study
phs000564
-
The genomic landscape of serrated lesion of the colorectum
Study
EGAS00001005648
-
Liverpool Preterm Birth Biomarker Study
Study
EGAS00001005076
-
TP53 variant detection analysis in high grade serous epithelial ovarian cancer
Study
EGAS00001004361
-
Genetic mutation profiling of lymphomas arising in the uterine cervix and vagina
Study
JGAS000823
-
RNA sequencing data of in vitro differentiated megakaryocyte cells transduced with E527K and WT SRC
Study
EGAS00001005808
-
Development of a diagnostic gene panel for Gorlin syndrome and its application to liquid biopsy
Study
JGAS000308
-
Singapore Adult Metabolism Study - Phase 2 (SAMS2)
Study
phs004078
-
Metatranscriptomic Sequencing of Pulmonary Fluid in Immunocompromised Children
Study
phs001684
-
Mapping and phasing of structural variation in patient genomes using nanopore sequencing
Study
EGAS00001002333
-
RaScALL: Rapid screening of RNA-seq in acute lymphoblastic leukaemia
Study
EGAS00001006460
-
The genomic and immune landscape of long-term survivors of high-grade serous ovarian cancer
Study
EGAS00001005984
-
We performed whole-exome sequencing of 20 samples (10 actinic keratosis and 10 cutaneous squamous cell carcinoma) to investigate a potential relationship between DNA methylation-based subtypes and genetic mutation patterns (Rodriguez-Paredes et al., Nat Commun 2017)
Study
EGAS00001002670
-
Whole genome, whole exome, and targeted sequencing of high-grade meningioma tumor samples.
Study
EGAS00001002294
-
Exploiting immune cell receptor information to quantify index switching in single cell transcriptome sequencing experiment
Study
EGAS00001002911
-
Comprehensive cancer predisposition gene testing in an adult multiple primary tumor series shows a broad range of deleterious variants and atypical tumor phenotypes
Dataset
EGAD00001004088
-
Characterization and clinical relevance of the genomic alterations defining invasive lobular breast cancer
Dataset
EGAD00001001395
-
A comprehensive characterization of the cell-free transcriptome reveals tissue- and subtype-specific biomarkers for cancer detection
Study
EGAS00001004704
-
Genome-Wide Association Study of Preterm Birth
Study
phs000332
-
The Neonatal Microbiome and Necrotizing Enterocolitis
Study
phs000247
-
Kids First: Whole Genome Sequencing in Recessive Structural Brain Defects
Study
phs002590
-
Application of Hi-C sequencing to detect structural variants in B-cell acute lymphoblastic leukemia
Study
EGAS00001005605
-
Genomic Landscape of Human Skin at a Single-Cell Resolution
Study
phs001979
-
Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing
Study
phs000858
-
Genetics of Schizophrenia in an Ashkenazi Jewish Case-Control Cohort
Study
phs000448
-
Early detection of ovarian cancer using cell-free DNA fragmentomes and protein biomarkers
Study
EGAS50000000484
-
Spatiotemporal Analysis of the Human Cerebellum
Study
phs001908
-
Genome-Wide Association Study of Genetic Susceptibility for Graft-vs-Host Disease Cohort 1
Study
phs002185
-
Sequence analysis of colorectal serrated lesions
Study
JGAS000217
-
Longitudinal copy number variation analysis from plasma DNA of head and neck cancer patients under re-radiotherapy
Study
EGAS50000000163
-
Whole genome sequencing to detect spontaneous acquired mutations in mismatch repair-deficient human colon organoids
Study
EGAS50000000114
-
The application of RNA sequencing for the diagnosis and genomic classification of pediatric acute lymphoblastic leukemia
Study
EGAS00001004212
-
The Genetic Landscape of Metastasis and Recurrence in Head and Neck Squamous Cell Carcinoma
Study
phs001007
-
The spectrum of somatic mutations in high-risk acute myeloid leukemia with -7/del(7q)
Study
phs000759
-
Next Generation Mendelian Genetics: Congenital Hyperinsulinism
Study
phs000539
-
Ultrasensitive Detection and Monitoring of Circulating Tumor DNA using Structural Variants in Early-Stage Breast Cancer
Study
EGAS50000000799
-
Copy number profiling of putative cancer stem from pleural effusion aspirates from breast cancer patients
Study
EGAS00001002343
-
Lenalidomide Resistance in del(5q) Myelodysplastic Syndrome Follows Loss of RUNX1/TP53-mediated Megakaryocytic Differentiation
Study
EGAS00001004113
-
Serial assessment of measurable residual disease in medulloblastoma liquid biopsies
Study
EGAS00001005592
-
Accurate detection of tumor-specific fusion genes reveals strongly immunogenic personal neo-antigens
Study
EGAS00001004877
-
Multi-Ethnic Study of Atherosclerosis (Echocardiogram Image Repository)
Study
phs003702
-
Single-cell DNA amplicon sequencing reveals clonal heterogeneity and evolution in T-cell acute lymphoblastic leukemia
Study
EGAS00001004440
-
Genome-Wide Association Studies of Prematurity and Its Complications (African American)
Study
phs000353
-
Direct Comparative Analysis of 10X Genomics Chromium and Smart-seq2
Study
EGAS00001003973
-
Differential Mutations in Matched Primary and Metastatic Colorectal Cancers
Study
phs001084
-
The Surveillance Monitoring for ART Toxicities (SMARTT) and the Women and Infants Transmission Study (WITS)
Study
phs002061
-
Whole genome sequencing and mutation rate analysis of Vietnamese trios with paternal dioxin exposure
Study
JGAS000137
-
Whole Genome Sequencing of HCC
Dataset
EGAD00001003994
-
Ten colorectal cancer patients with locally advanced primary tumors who underwent primary tumor resection following neoadjuvant chemotherapy (NAC).
Study
JGAS000222
-
Raw sequencing files from WGS and RNA-Seq
Study
EGAS50000000186
-
Clinical relevance of somatic copy-number alterations in plasma circulating tumor DNA from advanced EGFR-mutated NSCLC patients treated with osimertinib
Study
EGAS00001004539
-
Mutational Mechanisms in Multiply Relapsed Pediatric Acute Lymphoblastic Leukemia
Study
EGAS00001007900
-
Single-cell RNA sequencing of 16 NPM1 mutated AML patients
Study
EGAS50000000332
-
Multi-Ethnic Study of Atherosclerosis (Electrocardiogram Tracing Repository)
Study
phs003703
-
Total exRNA Profiles from Plasma, Saliva, and Urine of Healthy Subjects
Study
phs001258
-
Single molecule genome-wide mutation profiles of cell-free DNA for non-invasive detection of cancer
Study
EGAS00001007248
-
Cooperative Study of Sickle Cell Disease (CSSCD)
Study
phs002362
-
Detection and localization of surgically resectable cancers with a multi-analyte blood test
Study
EGAS00001002764
-
RaScALL: Rapid (Ra) screening (Sc) of RNA-seq data for prognostically significant genomic alterations in acute lymphoblastic leukaemia (ALL)
Dataset
EGAD00001009087
-
Single cell resolution landscape of hypomutated childhood cancers
Dataset
EGAD00001015406
-
Gabriella Miller Kids First Pediatric Research Program: An Integrated Clinical and Genomic Analysis of Treatment Failure in Pediatric Osteosarcoma
Study
phs001714
-
Center for Common Disease Genomics [CCDG] - Cardiovascular ATVB: Atherosclerosis Thrombosis and Vascular Biology
Study
phs001592
-
RNA-seq of Liver Cancer
Dataset
EGAD00001003993
-
Pre-activated anti-viral innate immunity in the upper airways controls early SARS-CoV-2 infection in children
Study
EGAS00001005461
-
High number of somatic mutations found in the healthy blood compartment of a 115-year-old woman reveals oligoclonal hematopoiesis
Study
EGAS00001000660
-
Phenotype and Genotype determination of 400 individuals from Northern Germany
Dataset
EGAD00001001315
-
Recurrent mTORC1-activating RRAGC mutations in follicular lymphoma
Study
EGAS00001001190