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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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