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Genomics

Bringing IGV webapp to Your Cloud Workspace in Seqera
Run IGV directly in your cloud workspace with automatic track discovery. Eliminate downloads and view genomic data where it lives. Open source proof of concept for Seqera Platform users.
Jan 16, 2026 3 min read Data at Scale
Microarray and deep sequencing cross-platform analysis of the mirRNome and isomiR variation in response to epidermal growth factor.
BACKGROUND: Epidermal Growth Factor (EGF) plays an important function in the regulation of cell growth, proliferation, and …
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A Pathogenic Mechanism in Huntington's Disease Involves Small CAG-Repeated RNAs with Neurotoxic Activity.
Huntington’s disease (HD) is an autosomal dominantly inherited disorder caused by the expansion of CAG repeats in the Huntingtin …
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Genome assembly comparison identifies structural variants in the human genome.
Numerous types of DNA variation exist, ranging from SNPs to larger structural alterations such as copy number variants (CNVs) and …
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