HELP

ac4C sites: fold enrichment >= 1, p value < 1e-04, and remove peaks that result from non-specific IgG binding, we intersected ac4C peaks with peaks called in IgG-IP, and kept only those that had no coordinate overlap.

Cite: Dynamic regulation of mRNA acetylation at synapses by learning and memory

At ac4Cat, the exploration never ceases. While our initial journey navigates through the mouse hippocampal regions, anticipate the unveiling of enriched, multi-regional neural datasets. Our evolving platform is a tapestry where each thread of data weaves deeper insights, enhancing the scholarly understanding of ac4C’s role and dynamic interplays across varied neural landscapes.

Experience the vibrancy of cutting-edge research as we unveil our enriching acRIP-seq and mRNA-seq results. In a dynamic confluence of genetic expressions and RNA-binding proteins, our curated datasets navigate through the labyrinth of ac4C modifications with utmost precision, adhering to the pinnacle of scientific rigor and integrity.

In the heart of ac4Cat lies a dedication to multifaceted synaptic scrutiny. With a focus that gracefully adapts and expands, our analyses illuminate the synaptic orchestration of ac4C modifications, aiming to offer a more holistic panorama of synaptic interactions and contributions across a spectrum of neural territories.

ac4Cat is not merely a platform but a living entity in the scientific exploration of ac4C modifications. With a design that breathes user-centric simplicity and an essence that vibrates with scientific vibrancy, we offer a navigation experience that is as enriching as it is effortless, allowing you to flow through updates and discoveries with unparalleled ease.

Embrace a journey marked by constant evolution, enriched perspectives, and an ever-widening horizon of ac4C discoveries across the vast and mysterious landscapes of neural biology.