Opportunity Overview
The emergence of next generation sequencing in the early 2000's led to so-called genome-wide studies focused on identifying individual variants associated with specific phenotypes. Such studies helped identify several variants associated with important phenotypic traits in plant and animal breeds. It also uncovered many variants linked to disease in humans. However much of the variation underlying these traits remains unexplained. Moreover, the increase in size of genomic datasets and complexity of traits being studied represent important challenges to the statistical frameworks in use.
It is now clear that complex phenotypic traits may be determined not only by many genes of small effect but also by so-called epistatic interactions among them. Some progress has been made in detecting interactions among a small number of variants but the role of high-order epistatic interactions still needs to be addressed. Thus, the challenge today is to develop new methods of analysis that can scale up to modern population genomics databases and uncover interactions between many genetic variants.
Our project addresses these challenges by harnessing the power of deep learning (DL) methods and complex network analysis (CNA) to develop an end-to-end computational tool to associate causal genetic variants to a phenotype of interest and also detect underlying epistatic interactions. Our approach will go beyond pairwise gene-to-gene interactions and study higher-order interactions.
We will implement DL models that scale up to high-dimensional input and...
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Start FreeSolicitation Details
| Issuing agency | BBSRC |
|---|---|
| Country | United Kingdom |
| Category | Training & Education |
| Published | March 01, 2026 |
| Procurement stage | Active solicitation |
| Response due | August 31, 2027 |
| Status | Open — accepting responses |
| Official source | View original notice |
| Last verified | August 12, 2026 |
Source: UK Research and Innovation (UKRI) — Open Government Licence v3.0.
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