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The nature of co-infection during outbreaks of infectious disease
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Exploring the Genetics and Biological Pathways of Obesity through Computational Biology and Statistical Approaches
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Developing enrichment analyzing methods at sub-cell type level to generate novel insights on complex disease pathogenesis
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A benchmark of rare cell type detection methods for single-cell RNA sequencing data
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Potential biomarkers for ALS/FTD as a consequence of TDP-43 loss of function
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Uncovering the contribution of rare genetic variants in orofacial clefts
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A Profiling of DNA Modifications in Neurodegenerative and Neuropsychiatric Disorders
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Examination of Brain Chromatin Accessibility in the Prairie Vole (Microtus ochrogaster)
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Analyzing the Developmental and Transcriptomic response of Callosobruchus maculatus to Alternative Bean Hosts
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Bayesian Functional Genome-wide Association Study using Standardized Individual-level and Summary-level GWAS Data
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EDClust: An EM-MM hybrid method for cell clustering in population-level single cell RNA sequencing
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The Disease-Associated Proteins Drosophila Nab2 and Ataxin-2 Interact with Shared RNAs and Coregulate Neuronal Morphology
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Identifying the causal variant of a rare skeletal disorder using whole-genome sequencing
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Roles of DNA methylation and hydroxymethylation in aging, immunosenescence, and gene regulation
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Integrating human brain transcriptomes and proteomes with genome-wide association data identifies risk genes shared between depression and Alzheimer’s disease
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Fundamental Principles of 3D Genomic Organization
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Maximizing the ability to detect modifying genetic factors of rare complex disorders – Fragile X-Associated Primary Ovarian Insufficiency and Down Syndrome - Congenital Heart Defects
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Genome-wide DNA methylation profile change in cancer cell lines under stresses
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Applying Genome-Wide Association Study to Analyze Novel Variants That Potentially Relate to Alzheimer’s Disease
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Integrative Prioritization of Genetic Loci for Nicotine Consumption
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