Generating Sequencing-Based DNA Methylation Maps from Low DNA Input Samples
Methods in Molecular Biology, ISSN: 1940-6029, Vol: 2458, Page: 3-21
2022
- 4Citations
- 2Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations4
- Citation Indexes4
- CrossRef1
- Captures2
- Readers2
Book Chapter Description
Reduced representation bisulfite sequencing (RRBS) is a technique used for assessing genome-wide DNA methylation patterns in eukaryotes. RRBS was introduced to focus on CpG-rich regions that are likely to be of most interest for epigenetic regulation, such as gene promoters and enhancer sequence elements (Meissner et al., Nature 454:766–770, 2008). This “reduced representation” lowers the cost of sequencing and also gives increased depth of coverage, facilitating the resolution of more subtle changes in methylation levels. Here, we describe a modified RRBS sequencing (RRBS-seq) library preparation. Our protocol is optimized for generating single base–resolution libraries when low input DNA is a concern (10–100 ng). Our protocol includes steps to optimize library preparation, such as using deparaffinization solution (when formalin-fixed material is used), and a replacement of gel size-selection with sample purification beads. The described protocol can be accomplished in 3 days and has been successfully applied to tissues or cells from different organisms, including formalin-fixed tissues, to yield robust and reproducible results.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85123966353&origin=inward; http://dx.doi.org/10.1007/978-1-0716-2140-0_1; http://www.ncbi.nlm.nih.gov/pubmed/35103959; https://link.springer.com/10.1007/978-1-0716-2140-0_1; https://dx.doi.org/10.1007/978-1-0716-2140-0_1; https://link.springer.com/protocol/10.1007/978-1-0716-2140-0_1
Springer Science and Business Media LLC
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