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NYU Dataset
SARS-CoV-2 Sequences from the NYU Langone Health COVID-19 Inpatient and Outpatient Population
- Authors
- Matthew T. MauranoSitharam RamaswamiPaul ZappileDacia Dimartino41 more author(s)...
- Description
The dataset includes 864 genomic sequences obtained from COVID-19 patients aged 18 years old and above within the NYU Langone Health system between March 12 and May 10, 2020. Patients reflected the health system's catchment area (i.e., the greater New York City metropolitan area). rRNA-depleted total RNA was sequenced, underwent quality control, and analyzed to produce phylogenetic trees. Further...
- Subject
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COVID-19GenomicsInfectious DiseaseRisk Factors
- Timeframe
- 2020
- Access Rights
- Free to AllApplication Required
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All of Us Research Hub
- Description
With an emphasis on reaching historically underrepresented populations, the All of Us Research Program recruits adults aged 18 and above across the United States to share their health data to enable new insights into human health and research on precision medicine. Participants contribute electronic health records (EHR), survey responses, biospecimens, wearable devices (biometrics), and physical measurements....
- Subject
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COVID-19Electronic Health RecordsGenomicsHealth Care SystemHealth StatusMental HealthPopulation CharacteristicsRisk Factors
- Access Rights
- Application RequiredAll NYU
- Local Expert
- Fred LaPolla
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NYU Dataset
Transposon Insertion Profiling by Sequencing (TIPseq) Utilized for LINE-1 Mapping in Single Cells
- Authors
- Wilson McKerrowZuojian TangJared P. SterankaLindsay M. Payer5 more author(s)...
- Description
This dataset was compiled to determine a genome-wide long interspersed element-1 (LINE-1) insertion site mapping method for bulk DNA. This study has shown that transposon insertion profiling by sequencing (TIPseq) is a method that can be used for LINE-1 mapping in single cells. Live GM12878 lymphoblastoid cells were used for this study. The dataset contains sequencing data as well as supplementary...
- Subject
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Genomics
- Access Rights
- Free to All
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NYU Dataset
Genetic Sequencing Data Characterized Genetic Etiology of Craniofacial Microsomia
- Authors
- Andrew T. TimberlakeCasey GriffinCarrie L. HeikeAnne V. Hing25 more author(s)...
- Description
This dataset was collected to study the genetic cause of craniofacial microsomia (CFM), which is the second most common congenital facial anomaly. In this study, they performed whole-exome or genome sequencing of 146 kindreds with sporadic (n = 138) or familial (n = 8) CFM. This is identified as a highly significant burden of loss of function variants in SF3B2, which is the most prevalent genetic cause...
- Subject
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Genomics
- Access Rights
- Free to All
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NYU Dataset
Whole Exome Sequencing Confirmed Progression of Smoldering Multiple Myeloma to Multiple Myeloma
- Authors
- Eileen M. BoyleShayu DeshpandeRuslana TytarenkoCody Ashby19 more author(s)...
- Description
Smoldering multiple myeloma (SMM) is an asymptomatic plasma cell disorder. It is associated with a high-risk of progression to multiple myeloma (MM). For this study, they performed targeted sequencing on 82 patients. The results showed fewer NRAS and FAM46C mutations with SMM, which is consistent with their role as drivers of the transition to MM. They also analyzed the change in clonal structure over...
- Subject
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CancerGenomics
- Access Rights
- Free to AllAuthor Approval Required
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Alzheimer’s Disease Neuroimaging Initiative
- Alternate Title(s)
- ADNI, ADNI1, ADNI GO, ADNI2, ADNI3
- Authors
- Michael W. Weiner
- Description
The Alzheimer’s Disease Neuroimaging Initiative (ADNI) began in 2004 as longitudinal multicenter study to identify clinical, imaging, genetic, and biochemical biomarkers for the detection and tracking of Alzheimer’s disease (AD). Participants are recruited from and followed at 59 research sites in the United States and Canada. ADNI1 enrolled 400 subjects who were diagnosed with mild cognitive impairment...
- Subject
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Chronic DiseaseGenomicsMental HealthNeuroscience
- Access Rights
- Free to AllApplication RequiredAuthor Approval Required
- Local Expert
- Omonigho M. BubuRicardo Osorio
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NYU Dataset
Clinical and genomic signatures of rising SARS-CoV-2 Delta breakthrough infections in New York
- Authors
- Ralf DuerrDacia DimartinoChristian MarierPaul Zappile10 more author(s)...
- Description
Investigators obtained high quality SARS-CoV-2 sequences from 132 vaccinated and 283 unvaccinated individuals who were seen at NYU Langone Health facilities between May 1, 2021 and August 3, 2021. Fully vaccinated individuals received either two doses of the BNT162b2 (Pfizer/BioNTech) or mRNA-1273 (Moderna) vaccines, or a single-dose of the COVID-19 Janssen vaccine. Breakthrough infections were defined...
- Subject
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COVID-19GenomicsInfectious Disease
- Timeframe
- 2021
- Access Rights
- Free to AllApplication Required
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Relating Clinical Outcomes in Multiple Myeloma to Personal Assessment of Genetic Profile Trial
- Alternate Title(s)
- CoMMpass
- Description
The Relating Clinical Outcomes in MM to Personal Assessment of Genetic Profile (CoMMpass) trial is a longitudinal observational study sponsored by the Multiple Myeloma Research Foundation (MMRF) which follows adult patients with newly diagnosed and symptomatic myeloma over a 10 year period. The study began in 2011 and has enrolled 1154 participants across the United States, Canada, and Spain. Study...
- Subject
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CancerGenomics
- Access Rights
- Free to AllApplication Required
- Local Expert
- Gareth J. Morgan
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NYU Dataset
Isolation of Clostridia from the Gut Microbiome of Helminth-Colonized Humans
- Authors
- Shushan SargsianZe ChenSoo Ching LeeAmicha Robertson14 more author(s)...
- Description
Helminth colonization has been associated with altered composition of the gut microbiota, such as increases in Clostridia. However, it is unclear if specific bacterial species display differential effects on helminth reproduction. This study isolated and sequenced the genome of 13 Clostridia from the Orang Asli, an indigenous population in Malaysia with a high prevalence of helminth infections. Metagenomic...
- Subject
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Genomics
- Access Rights
- Free to All