Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

ABSTRACT: Biomarkers of Vaccine Immunosafety (BioVacSafe) - Study CRC305B

PROVIDER: PRJNA492829 | ENA |

REPOSITORIES: ENA

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
	SRR7893490.fastq.gz	Fastqsanger.gz
	SRR7893500.fastq.gz	Fastqsanger.gz
	SRR7893510.fastq.gz	Fastqsanger.gz
	SRR7893520.fastq.gz	Fastqsanger.gz
	SRR7893530.fastq.gz	Fastqsanger.gz

Items per page:

1 - 5 of 766

Similar Datasets

Project description:Biomarkers of Vaccine Immunosafety (BioVacSafe) - Study CRC305A

| PRJNA492827 | ENA

Project description:Biomarkers of Vaccine Immunosafety (BioVacSafe) - Study CRC305C

| PRJNA492965 | ENA

Project description:Biomarkers of Vaccine Immunosafety (BioVacSafe)

| PRJNA515032 | ENA

BioVacSafe (Biomarkers for enhanced vaccine immunosafety) Influenza challenge

Project description:BioVacSafe (Biomarkers for enhanced vaccine immunosafety) Influenza challenge

| PRJNA732702 | ENA

Biomarkers for canine Leptospira vaccine potency

Project description:Biomarkers for canine Leptospira vaccine potency

| PRJNA793869 | ENA

Identification of Biomarkers of Vaccine Reactogenicity

Project description:Identification of Biomarkers of Vaccine Reactogenicity

| PRJNA494386 | ENA

Immune profiles identification by vaccinomics after MVA immunization in randomized clinical study

Project description:Whole blood transcriptomics analysis of healthy individuals, immunized with the MVA-B vaccine via transcutaneous or intramuscular route. We define an early gene expression profile, detected at day 1 and day 7 after immunization, that is associated with the development of either MVA specific humoral or CD8 T cell responses. We used System Biology approach to analyse vaccine efficacy in order to find innate predictive biomarkers of the quality of adaptive responses for potential clinical use in the future. Moreover, from a methodological point of view this study increases knowledges on how vaccine route(s) can affect resulting immune responses and into mechanisms involved in the induction of humoral and cellular immunity to vaccine.

2020-10-30 | E-MTAB-9642 | biostudies-arrayexpress

Innate gene signature distinguishes humoral versus cytotoxic responses to influenza vaccination

Project description:Whole blood transcriptomics analysis of healthy individuals, immunized with the trivalent 2012-2013 season flu vaccine via transcutaneous, intramuscular or intradermal route. We define an early gene expression profile, detected at day 1 after immunization, that is associated with the development of either humoral or cytotoxic CD8 T cell responses. We used System Biology approach to analyse vaccine efficacy in order to find innate predictive biomarkers of the quality of adaptive responses for potential clinical use in the future. Moreover, from a methodological point of view this study increases knowledges on how vaccine route(s) can affect resulting immune responses and into mechanisms involved in the induction of humoral and cellular immunity to influenza vaccination.

2019-07-01 | E-MTAB-7741 | biostudies-arrayexpress

Genome-wide profiling of whole blood from healthy adult volunteers before and after receiving non-live vaccines including seasonal influenza or pneumococcal vaccine or placebo (saline) injections I

Project description:The objective of this study is to: 1) Characterize the cellular origin of transciptional signatures observed on day 1 after vaccination with 2009/10 seasonal influenza and pneumococcal vaccine discovered by transcriptional profiling of whole blood samples in data set “WholeBlood_SysVax”. 2) Discover potential biomarkers for immune-responsiveness to non-live vaccines.

2013-07-10 | GSE30059 | GEO

Transcriptional profiling of YF-naïve participants after vaccination against yellow fever.

Project description:Mechanisms of poor responses to vaccines remain unknown. Yellow fever-naïve adults were vaccinated with a yellow fever vaccine (YF-17D, Stamaril). Transcriptomic profilling of blood collected pre-vaccination and post-vaccination (day 3, 7, 14 and 84) was performed in order to identify candidate biomarkers of antibody response to the vaccine.

2020-05-19 | GSE136163 | GEO

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data