@bvhalldorsson Great paper. Could you share your SV calling pipeline using DRAGEN 3.7.8, along with the number of duplications detected per individual?
Thrilled to share the bulk of my PhD work, now up on bioRxiv!
This project brings together aspects of network theory, systems biology, and single cell genomics, towards understanding properties of gene regulatory networks (GRNs). Read on for more —> (1/)
https://t.co/RY1syLiS6S
@jxchong For Eagle 2, the reference-based phasing is performed on a target set with reference panel .If Ntarget < Nref/2, Eagle2 performs only one phasing iteration. The few iteration maybe affect the accuracy
Congratulations to @NancyGenetics, director of the @VUMCgenetics, for receiving the 2023 ASHG Leadership Award from the American Society of Human Genetics (@GeneticsSociety).
https://t.co/4LVfOSI5YH
Ting’s paper is out. @TingQi2 Leveraging a powerful new method and large datasets, we established a comprehensive genetic regulation map of RNA splicing, which helped to reveal a distinct and essential role of RNA splicing in common traits and diseases. https://t.co/eXxHNIl3WD
Congratulations @JDMosley_Moses and @DriestSara! Great to see your important work recognized as a key advance in genomic medicine @VUMChealth @VUMCgenetics @vumcdbmi https://t.co/2lJb0IV42R
@Joni_Coleman @Andrew_Grotz In my opinion, ldsc and simple linear model seems to have the similar assumption, however Regenie obtains the summary statistics with whole genome regression model
Polygenic Scores for Cognitive Abilities and their Association with Different Aspects of General Intelligence - a Deep Phenotyping Approach https://t.co/2K9QbtXCrN