This project will create intelligent systems for personalized and precise risk prediction and diagnosis of non-communicable diseases using multi-omics data, by developing, implementing and validating novel algorithms for structure learning and inference in large-scale, multi-organ causal Bayesian gene networks, based on computational methods that we have developed previously to infer, characterize and validate gene regulatory networks in complex diseases.
More information can be found in the NFR project bank.
Group members involved
- Sean Bankier (postdoc, 2021-2024)
- Gutama Ibrahim (PhD student, 2022-2024)
- Mariyam Khan (PhD student, 2021-2023)
Date
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Title
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Nov 25, 2024
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Bioinformatics Advances paper
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Nov 11, 2024
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PLOS Genetics paper
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Oct 31, 2024
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Young Scientist Award to Sean
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Aug 19, 2024
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Gene expression prediction using GRNs preprint
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Feb 6, 2024
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Findr in Julia is now BioFindr
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Jan 15, 2024
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MVMR with correlated instruments preprint
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Nov 1, 2023
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Mariyam presents TRACE seminar
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Aug 22, 2023
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Causal inference in drug discovery review
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Aug 22, 2023
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FlowGAT preprint
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Aug 21, 2023
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Findr in Julia
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Jun 28, 2023
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Helmholtz grant to Mariyam
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Jun 6, 2023
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Sean speaks at ENDO
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Jun 6, 2023
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Sean and Adriaan presented at GRN meeting
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Jan 25, 2023
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Mariyam interviewed by UiB AI News
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Jan 24, 2023
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Cortisol-responsive gene networks preprint
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Nov 9, 2022
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Sean speaks at Exercise in Medicine workshop
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Nov 9, 2022
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Mariyam speaks at NORA Research School Annual Conference
|
Nov 9, 2022
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Research stay abroad funding to Mariyam
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Oct 12, 2022
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Erasmus+ funding to Sean
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Oct 12, 2022
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Mariyam presents at ICSB 2022
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Sep 30, 2022
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Causal inference in drug discovery preprint
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Sep 16, 2022
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Sean attends EMBO multi-omics course
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Sep 1, 2022
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NORA-Turing exchange fellowship to Mariyam
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Aug 17, 2022
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eQTL networks review
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Mar 23, 2022
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Welcome Gutama!
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Sep 22, 2021
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Congratulations Sean!
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Sep 10, 2021
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PhD position available
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Mar 8, 2021
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Welcome Mariyam!
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Nov 3, 2020
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PhD and postdoc position available
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Oct 15, 2020
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INTRePID project funded by NFR
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