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| 37577719 | EpiVar Browser: advanced exploration of epigenomics data under controlled access. | bioRxiv | 2023 |
| 37576549 | Glucocorticoid stimulation induces regionalized gene responses within topologically associating domains. | Front Genet | 2023 |
| 37599818 | Selection for immune evasion in SARS-CoV-2 revealed by high-resolution epitope mapping and sequence analysis. | iScience | 2023 |
| 37170172 | Capturing sex-specific and hypofertility-linked effects of assisted reproductive technologies on the cord blood DNA methylome. | Clin Epigenetics | 2023 |
| 37228757 | Transposable elements are associated with the variable response to influenza infection. | Cell Genom | 2023 |
| 37228750 | Genome graphs detect human polymorphisms in active epigenomic state during influenza infection. | Cell Genom | 2023 |
| 37131148 | HostSeq: a Canadian whole genome sequencing and clinical data resource. | BMC Genom Data | 2023 |
| 37395395 | ZMYM2 is essential for methylation of germline genes and active transposons in embryonic development. | Nucleic Acids Res | 2023 |
| 36449159 | A Pangenome Approach to Detect and Genotype TE Insertion Polymorphisms. | Methods Mol Biol | 2023 |
| 36449158 | Genotyping of Transposable Element Insertions Segregating in Human Populations Using Short-Read Realignments. | Methods Mol Biol | 2023 |
| 36815791 | Application of Genomic Sequencing to Refine Patient Stratification for Adjuvant Therapy in Renal Cell Carcinoma. | Clin Cancer Res | 2023 |
| 34996498 | Integrative analysis of 3604 GWAS reveals multiple novel cell type-specific regulatory associations. | Genome Biol | 2022 |
| 35547873 | Intra-Tumoral CD8+ T-Cell Infiltration and PD-L1 Positivity in Homologous Recombination Deficient Pancreatic Ductal Adenocarcinoma. | Front Oncol | 2022 |
| 35648852 | A systems biology approach identifies candidate drugs to reduce mortality in severely ill patients with COVID-19. | Sci Adv | 2022 |
| 35720974 | PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions. | Cell Genom | 2022 |
| 35416251 | Glioblastoma scRNA-seq shows treatment-induced, immune-dependent increase in mesenchymal cancer cells and structural variants in distal neural stem cells. | Neuro Oncol | 2022 |
| 36611933 | Identification of R-Spondin Gene Signature Predictive of Metastatic Progression in BRAFV<sup>600E</sup>-Positive Papillary Thyroid Cancer. | Cells | 2022 |
| 36337358 | More than a 'Hundred Days War': Persistent SARS-CoV-2 infection in a patient with ANCA-associated vasculitis. | J Assoc Med Microbiol Infect Dis Can | 2022 |
| 35863436 | The amino acid sensor GCN2 suppresses terminal oligopyrimidine (TOP) mRNA translation via La-related protein 1 (LARP1). | J Biol Chem | 2022 |
| 36327219 | Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative. | PLoS Genet | 2022 |
| 35188098 | Application of ATAC-Seq for genome-wide analysis of the chromatin state at single myofiber resolution. | Elife | 2022 |
| 33433612 | Invasive growth associated with cold-inducible RNA-binding protein expression drives recurrence of surgically resected brain metastases. | Neuro Oncol | 2021 |
| 36778585 | CanDIG: Federated network across Canada for multi-omic and health data discovery and analysis. | Cell Genom | 2021 |
| 33521749 | Cell-free DNA tissues of origin by methylation profiling reveals significant cell, tissue, and organ-specific injury related to COVID-19 severity. | Med | 2021 |
| 33654212 | Publisher Correction: Single-cell analysis of childhood leukemia reveals a link between developmental states and ribosomal protein expression as a source of intra-individual heterogeneity. | Sci Rep | 2021 |
| 33731361 | Ultrafast functional profiling of RNA-seq data for nonmodel organisms. | Genome Res | 2021 |
| 35072136 | GA4GH: International policies and standards for data sharing across genomic research and healthcare. | Cell Genom | 2021 |
| 34590283 | Inferring Copy Number from Triple-Negative Breast Cancer Patient Derived Xenograft scRNAseq Data Using scCNA. | Methods Mol Biol | 2021 |
| 34706766 | A small number of early introductions seeded widespread transmission of SARS-CoV-2 in Québec, Canada. | Genome Med | 2021 |
| 34731633 | Inherent genomic properties underlie the epigenomic heterogeneity of human induced pluripotent stem cells. | Cell Rep | 2021 |
| 34811454 | Author Correction: Distinct roles of androgen receptor, estrogen receptor alpha, and BCL6 in the establishment of sex-biased DNA methylation in mouse liver. | Sci Rep | 2021 |
| 34043590 | Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19. | J Clin Invest | 2021 |
| 34215813 | Distinct roles of androgen receptor, estrogen receptor alpha, and BCL6 in the establishment of sex-biased DNA methylation in mouse liver. | Sci Rep | 2021 |
| 34289352 | Whole-genome sequencing of H3K4me3 and DNA methylation in human sperm reveals regions of overlap linked to fertility and development. | Cell Rep | 2021 |
| 33976190 | A coordinated progression of progenitor cell states initiates urinary tract development. | Nat Commun | 2021 |
| 34335193 | Single Cell Transcriptomics of Ependymal Cells Across Age, Region and Species Reveals Cilia-Related and Metal Ion Regulatory Roles as Major Conserved Ependymal Cell Functions. | Front Cell Neurosci | 2021 |
| 34194450 | The Cowpea Kinome: Genomic and Transcriptomic Analysis Under Biotic and Abiotic Stresses. | Front Plant Sci | 2021 |
| 31591503 | A point mutation in the linker domain of mouse STAT5A is associated with impaired NK-cell regulation. | Genes Immun | 2020 |
| 32056496 | Developmental genome-wide DNA methylation asymmetry between mouse placenta and embryo. | Epigenetics | 2020 |
| 32075553 | Transposable elements have contributed human regulatory regions that are activated upon bacterial infection. | Philos Trans R Soc Lond B Biol Sci | 2020 |
| 32066997 | Single-cell analysis of human adipose tissue identifies depot and disease specific cell types. | Nat Metab | 2020 |
| 31797611 | Machine learning algorithms for simultaneous supervised detection of peaks in multiple samples and cell types. | Pac Symp Biocomput | 2020 |
| 33168820 | Paired rRNA-depleted and polyA-selected RNA sequencing data and supporting multi-omics data from human T cells. | Sci Data | 2020 |
| 33398295 | Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19. | medRxiv | 2020 |
| 32766608 | Cell-Free DNA in Blood Reveals Significant Cell, Tissue and Organ Specific injury and Predicts COVID-19 Severity. | medRxiv | 2020 |
| 32527045 | Sex Chromosomes and Sex Phenotype Contribute to Biased DNA Methylation in Mouse Liver. | Cells | 2020 |
| 32415257 | Single-cell analysis of childhood leukemia reveals a link between developmental states and ribosomal protein expression as a source of intra-individual heterogeneity. | Sci Rep | 2020 |
| 32450900 | Personalized and graph genomes reveal missing signal in epigenomic data. | Genome Biol | 2020 |
| 30582441 | Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot. | Circ Res | 2019 |