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Screening and Functional Validation of Human Birth Defects Genomic Variants (R01 Clinical Trial not Allowed)

USARFP notice for Screening and Functional Validation of Human Birth Defects Genomic Variants (R01 Clinical Trial not Allowed). The reference ID of the tender is 52847012 and it is closing on 07 May 2025.

Tender Details

  • Country: USA
  • Summary: Screening and Functional Validation of Human Birth Defects Genomic Variants (R01 Clinical Trial not Allowed)
  • UST Ref No: 52847012
  • Deadline: 07 May 2025
  • Financier: Self Financed
  • Purchaser Ownership: Government
  • Tender Value: Refer Document
  • Notice Type: Tender
  • Document Ref. No.: PAR-21-229
  • Purchaser's Detail:
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  • Description:
  • Tender are invited for Screening and Functional Validation of Human Birth Defects Genomic Variants (R01 Clinical Trial Not Allowed)
    CFDA Number : 93.121 -- Oral Diseases and Disorders Research93.351 -- Research Infrastructure Programs93.865 -- Child Health and Human Development Extramural Research
    Cost Sharing or Matching Requirement : No
    Closing Date for Applications: May 07, 2025
    Posted Date : May 05, 2021
    Description: Rapid advances in genotyping and next generation sequencing technologies have led to the identification of genetic variants that are associated with a wide variety of congenital defects including structural birth defects (SBDs), intellectual developmental disabilities (IDDs) and inborn errors of metabolism (IEMs). Large quantities of genomic data collected from pediatric birth defects cohorts are available to the research community through several databases such as the Database of Genotypes and Phenotypes (dbGaP), the Gabriella Miller Kids First Data Resource Portal, the European Genome-Phenome Archive and Clinical Genome Resource (ClinGen). The purpose of this initiative is to promote the screening, functional validation and characterization of birth defects-associated genetic variants identified through public facing databases and individual efforts using in-silico tools, appropriate animal models, in vitro systems or multi-pronged approaches. This initiative addresses a challenging gap between identify...
  • Documents:

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Screening and Functional Validation of Human Birth Defects Genomic Variants (R01 Clinical Trial not Allowed) - USA Tender

The NATIONAL INSTITUTES OF HEALTH, a Government sector organization in USA, has announced a new tender for Screening and Functional Validation of Human Birth Defects Genomic Variants (R01 Clinical Trial not Allowed). This tender is published on USARFP under UST Ref No: 52847012 and is categorized as a Tender. Interested and eligible suppliers are invited to participate by reviewing the tender documents and submitting their bids before the deadline on 2025-05-07.

The estimated tender value is Refer Document, and full details, including technical specifications and submission requirements, are provided in the official tender documents. Ensure all submissions meet the criteria outlined to be considered for evaluation.

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