| identifier: | SDY508 |
| description: |
Integrate two high-throughput technologies namely, microengraving-based screening of primary B cells and next-generation sequencing to examine the relationship between the diversity and quality of humoral responses raised and the severity of disease.
|
| aggregation: |
instance of dataset
|
| availability: |
available with registration
|
| acknowledges: |
NIAID (HIPC funded)
|
| isAbout: |
Determine how humoral responses relate to severity of disease to provide insight to predicting outcomes.
|
| authorizations: |
registration required
|
| landingPage: |
https://www.immunespace.org/project/Studies/SDY508/begin.view? |
| subject species: | Homo sapiens |
| study conditions: | West Nile virus |
| study type: | Observational |
| study category: | Immune Response |
| assay type: | |
| time point: | |
| subject race: |
Black or African American White |
| subject gender: |
Female Male |
| subject age: |
21-30 31-40 41-50 51-60 61-70 |
| name: |
Antibody responses to infection with West Nile virus
|
| affiliations: |
Yale
|
| fullName: |
David Hafler
|
| roles: |
principal investigator
|
| name: |
Humoral responses to West Nile virus
|
| size: |
12
|
| output: |
Next-generation sequencing for pools of B cells isolated from subject.
|
| description: |
Integrate two high-throughput technologies namely, microengraving-based screening of primary B cells and next-generation sequencing to examine the relationship between the diversity and quality of humoral responses raised and the severity of disease.
|
| name: |
ImmuneSpace
|
| homePage: |
http://www.immunespace.org |