Fig. 5: Transcriptional consequences of rare CNVs can be significantly predicted.
From: Functional annotation of rare structural variation in the human brain
SV expression prediction performance and associated R2 from building the same linear model using different training and test datasets. a CMC into CMC_HBCC, b CMC_HBCC into CMC, c CMC into CMC, and d CMC_HBCC into CMC_HBCC. The best fit line with confidence interval was produced using generalized additive model smoothing.
