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Nature Genetics|September 30, 2024
Valid inference for machine learning-assisted genome-wide association studiesJiacheng Miao, Yixuan Wu, Zhongxuan Sun, et al.Nature Genetics|September 16, 2024
Interpreting cis-regulatory interactions from large-scale deep neural networksShushan Toneyan, Peter K KooNature Genetics|September 25, 2024
Integration of variant annotations using deep set networks boosts rare variant association testingBrian Clarke, Eva Holtkamp, Hakime Öztürk, et al.Nature Genetics|September 23, 2024
A phenome-wide association study of methylated GC-rich repeats identifies a GCC repeat expansion in AFF3 associated with intellectual disabilityBharati Jadhav, Paras Garg, Joke J F A van Vugt, et al.Nature Genetics|September 24, 2024
Statistically and functionally fine-mapped blood eQTLs and pQTLs from 1,405 humans reveal distinct regulation patterns and disease relevanceQingbo S Wang, Takanori Hasegawa, Ho Namkoong, et al.Nature Genetics|September 10, 2024
Variants in tubule epithelial regulatory elements mediate most heritable differences in human kidney functionGabriel B Loeb, Pooja Kathail, Richard W Shuai, et al.Nature Genetics|March 12, 2024
Enhancer-promoter interactions become more instructive in the transition from cell-fate specification to tissue differentiationTim Pollex, Adam Rabinowitz, Maria Cristina Gambetta, et al.Nature Genetics|March 7, 2024
MYC activity at enhancers drives prognostic transcriptional programs through an epigenetic switchSimon T Jakobsen, Rikke A M Jensen, Maria S Madsen, et al.Nature Genetics|February 29, 2024
Epigenetic variation impacts individual differences in the transcriptional response to influenza infectionKatherine A Aracena, Yen-Lung Lin, Kaixuan Luo, et al.Nature Genetics|February 27, 2024
BANKSY unifies cell typing and tissue domain segmentation for scalable spatial omics data analysisVipul Singhal, Nigel Chou, Joseph Lee, et al.Pageof 744