Over the past decades, large-scale human genetic studies have identified numerous risk genes and variants associated with complex diseases and traits.
In a recent study posted to the bioRxiv* preprint server, researchers developed and elucidated a ‘bridge integration’ method to harmonize single-cell ribonucleic acid (RNA) sequencing (scRNA-seq) ...
Results that may be inaccessible to you are currently showing.
Hide inaccessible results
Feedback