dbGaP, the database of Genotypes and Phenotypes This is an RSS file. You can use it to subscribe to this data in your favourite RSS reader or to display this data on your own website or blog.

New | phs002826.v1.p1 | Analysis of Papilloma Infiltrating T cells from an Exceptional Responder to Immunotherapy
Analysis of Papilloma Infiltrating T cells from an Exceptional Responder to Immunotherapy  (study page |release notes) (Source: dbGaP, the database of Genotypes and Phenotypes)
Source: dbGaP, the database of Genotypes and Phenotypes - August 18, 2023 Category: Genetics & Stem Cells Tags: StudyRelease Source Type: research

New | phs002480.v3.p3 | Genomics of Glomerular Disorders
​ Genomics of Glomerular Disorders  (study page |release notes) (Source: dbGaP, the database of Genotypes and Phenotypes)
Source: dbGaP, the database of Genotypes and Phenotypes - August 17, 2023 Category: Genetics & Stem Cells Tags: StudyRelease Source Type: research

New | phs003260.v1.p1 | Single Nucleus Transcriptomes from the Ventral Midbrain of Opioid Overdose Cases and Controls
​ Single Nucleus Transcriptomes from the Ventral Midbrain of Opioid Overdose Cases and Controls  (study page |release notes) (Source: dbGaP, the database of Genotypes and Phenotypes)
Source: dbGaP, the database of Genotypes and Phenotypes - August 17, 2023 Category: Genetics & Stem Cells Tags: StudyRelease Source Type: research

New | phs002189.v1.p1 | Merkel Cell Carcinoma Tissue and Data Repository
​ Merkel Cell Carcinoma Tissue and Data Repository  (study page |release notes) (Source: dbGaP, the database of Genotypes and Phenotypes)
Source: dbGaP, the database of Genotypes and Phenotypes - August 17, 2023 Category: Genetics & Stem Cells Tags: StudyRelease Source Type: research

New | phs002005.v1.p1 | MP2PRT: Comprehensive Genomic Profiling to Identify Alterations Associated with Relapse for NCI Standard Risk (SR) B-Lineage ALL and NCI High Risk (HR) B-Lineage ALL with Favorable Genetic Features
MP2PRT: Comprehensive Genomic Profiling to Identify Alterations Associated with Relapse for NCI Standard Risk (SR) B-Lineage ALL and NCI High Risk (HR) B-Lineage ALL with Favorable Genetic Features  (study page |release notes) (Source: dbGaP, the database of Genotypes and Phenotypes)
Source: dbGaP, the database of Genotypes and Phenotypes - August 16, 2023 Category: Genetics & Stem Cells Tags: StudyRelease Source Type: research