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Medrxiv : the Preprint Server for Health Sciences|April 2, 2024
Mapping structural variants to rare disease genes using long-read whole genome sequencing and trait-relevant polygenic scoresCas LeMaster, Carl Schwendinger-Schreck, Bing Ge, et al.Plos Computational Biology|June 15, 2007
A survey of genomic properties for the detection of regulatory polymorphismsStephen B Montgomery, Obi L Griffith, Johanna M Schuetz, et al.Plos One|June 12, 2012
Genotype-based test in mapping cis-regulatory variants from allele-specific expression dataJean Francois Lefebvre, Emilio Vello, Bing Ge, et al.Genome Research|August 25, 2011
DNA methylation profiles of human active and inactive X chromosomesAndrew J Sharp, Elisavet Stathaki, Eugenia Migliavacca, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|November 28, 2020
Evaluating the Genomic Parameters Governing rAAV-Mediated Homologous RecombinationLaura P Spector, Matthew Tiffany, Nicole M Ferraro, et al.Nature Methods|November 26, 2013
Quantifying RNA allelic ratios by microfluidic multiplex PCR and sequencingRui Zhang, Xin Li, Gokul Ramaswami, et al.JCI Insight|June 22, 2021
The role of Sp140 revealed in IgE and mast cell responses in Collaborative Cross miceKazufumi Matsushita, Xin Li, Yuki Nakamura, et al.Biorxiv : the Preprint Server for Biology|May 15, 2024
regionalpcs: improved discovery of DNA methylation associations with complex traitsTiffany Eulalio, Min Woo Sun, Olivier Gevaert, et al.American Journal of Human Genetics|January 11, 2016
An Efficient Multiple-Testing Adjustment for eQTL Studies that Accounts for Linkage Disequilibrium between VariantsJoe R Davis, Laure Fresard, David A Knowles, et al.Nature Communications|January 3, 2025
regionalpcs improve discovery of DNA methylation associations with complex traitsTiffany Eulalio, Min Woo Sun, Olivier Gevaert, et al.Pageof 20