Select Publications
Preprints
2024, Chromatin remodeling with combined FACT and BET inhibition disrupts oncogenic transcription in Diffuse Midline Glioma, http://dx.doi.org/10.1101/2024.06.06.597703
,2024, Genes in Humans and Mice: Insights from Deep learning of 777K Bulk Transcriptomes, http://dx.doi.org/10.1101/2024.04.01.587517
,2024, Multifaceted Representation of Genes via Deep Learning of Gene Expression Networks, http://dx.doi.org/10.1101/2024.03.07.583777
,2023, Evolutionary conservation of embryonic DNA methylome remodelling in distantly related teleost species, http://dx.doi.org/10.1101/2023.05.24.542066
,2022, Environmental and genetic disease modifiers of haploinsufficiency of A20, http://dx.doi.org/10.1101/2022.03.19.485004
,2022, Human genomic DNA is widely interspersed with i-motif structures, http://dx.doi.org/10.1101/2022.04.14.488274
,2020, ClinSV: Clinical grade structural and copy number variant detection from whole genome sequencing data, http://dx.doi.org/10.1101/2020.06.30.20143453
,2018, The Medical Genome Reference Bank: a whole-genome data resource of 4,000 healthy elderly individuals. Rationale and cohort design, http://dx.doi.org/10.1101/274019
,2017, Universal alternative splicing of noncoding exons, http://dx.doi.org/10.1101/136275
,2016, Machine-learning annotation of human splicing branchpoints, http://dx.doi.org/10.1101/094003
,2016, RNA-seq reveals more consistent reference genes for gene expression studies in human non-melanoma skin cancers, http://dx.doi.org/10.7287/peerj.preprints.2331
,2016, RNA-seq reveals more consistent reference genes for gene expression studies in human non-melanoma skin cancers, http://dx.doi.org/10.7287/peerj.preprints.2331v1
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