Our abstract titled "NERINE: Network-based association test for rare variants in complex traits and diseases" has been accepted for oral presentation at the "Machine Learning and Statistics" session of the ESHG 2024, Berlin, Germany. The talk is scheduled to happen on June 4,...
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"The authors use whole-exome germ line sequencing to analyze whether a set of 27 complement genes is associated with PF. Uncovering much-needed new pathophysiological clues could enable better therapy for patients with PF in the future, but finding new and meaningful connections from a haystack...
Check out our latest preprint titled "Deep sequencing of proteotoxicity modifier genes uncovers a Presenilin-2/beta-amyloid-actin genetic risk module shared among alpha-synucleinopathies." Link to the study: https://www....
Speaker: Sumaiya Nazeen
Title: "Network-based approaches for rare variant association in complex diseases"
Related Article: ...
Talk title: Network-based approaches for rare variant association in complex diseases
Lab: Sunyaev
Time: 9:30 - 11 am
Our manuscript titled "Low-frequency inherited complement receptor variants are associated with purpura fulminans" have been accepted in Blood.
Link to medRxiv preprint: https://doi.org/10.1101/2022.02.24.22271459
Talk Title: Network-based rare variant association testing in dichotomous traits
Talk title: Computational Biology in the 21st Century: Untangling Health and Disease
Abstract: Computational biology is a discipline that lies at the intersection of computer science and life sciences. It has been a game changer for life sciences research in myriad ways in recent years....
Our manuscript titled "The missing link between genetic association and regulatory function" has been accepted for publication in eLife. This study, led by Noah Connally, investigates whether the baseline expression of trait-related genes explains GWAS associations. We tested different...
Read the full twitter thread at the following link:
https://twitter.com/CellCellPress/status/1613951138432258083
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