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Examine the impact of epigenomic modifications that cause diseases and disorders in plants, animals, and humans.
What is Epigenomics?
Epigenomics is the study of epigenetic changes — such as chromatin assembly, histone modification, and DNA-protein interaction — in a cell.
These modifications are different between different cell types and can affect gene translation and gene expression without changing the DNA sequence.
Why is Studying Epigenomics Important?
Genetic disorders, metabolic disorders, cancers, degenerative diseases, and changes in plant plasticity have all been linked to epigenetic errors.
Studying the locations and understanding how reversible compound interactions influence genome expression can help scientists recognize the mechanisms by which genes are turned on or off in disease.
What Can You Do?
Build a comprehensive epigenetic analysis to identify new biomarkers and therapeutic targets.
Understand the role heritability, environment, and behavior play in gene expression and cell differentiation.
Tools for Studying Epigenomics
Whole Genome Bisulfite Sequencing (WGBS)
Reduced Representation Bisulfite Sequencing (RRBS)
Chromatin Immunoprecipitation Sequencing (ChIP-Seq)
Assay for Transposase Accessible Chromatin Sequencing (ATAC-Seq)
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Get in touch with your local field team and start designing a project. We’ll help drive your research forward with the right tools for your investigative needs.
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At this step you'll be able to keep an eye on all the various methods and platforms we’re using to ensure your starting material will produce the most in-depth information possible. It’s easy to get in touch with us if you have a question or concern.
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Securely access your raw data and view detailed analyses specific to your scientific question all in one place. Then reach out to our bioinformatics scientists to dig deeper into the results.
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More PSOmics Solutions
Epigenomics is just one field of study within the omics landscape. Learn how we are helping answer specific questions in other areas.