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HandWiki. Illumina Dye Sequencing. Encyclopedia. Available online: https://encyclopedia.pub/entry/30840 (accessed on 25 September 2026).
HandWiki. Illumina Dye Sequencing. Encyclopedia. Available at: https://encyclopedia.pub/entry/30840. Accessed September 25, 2026.
HandWiki. "Illumina Dye Sequencing" Encyclopedia, https://encyclopedia.pub/entry/30840 (accessed September 25, 2026).
HandWiki. (2022, October 24). Illumina Dye Sequencing. In Encyclopedia. https://encyclopedia.pub/entry/30840
HandWiki. "Illumina Dye Sequencing." Encyclopedia. Web. 24 October, 2022.
Illumina Dye Sequencing
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The content is sourced from: https://handwiki.org/wiki/Biology:Illumina_dye_sequencing

Illumina dye sequencing is a technique used to determine the series of base pairs in DNA, also known as DNA sequencing. The reversible terminated chemistry concept was invented by Bruno Canard and Simon Sarfati at the Pasteur Institute in Paris. It was developed by Shankar Balasubramanian and David Klenerman of Cambridge University, who subsequently founded Solexa, a company later acquired by Illumina. This sequencing method is based on reversible dye-terminators that enable the identification of single nucleotides as they are washed over DNA strands. It can also be used for whole-genome and region sequencing, transcriptome analysis, metagenomics, small RNA discovery, methylation profiling, and genome-wide protein-nucleic acid interaction analysis.

illumina solexa methylation

References

  1. Clark, David P.,. Molecular biology. Pazdernik, Nanette Jean,, McGehee, Michelle R., (Third ed.). London. ISBN 978-0-12-813289-0. OCLC 1062496183. https://www.worldcat.org/oclc/1062496183. 
  2. "Illumina sequencing library preparation for highly multiplexed target capture and sequencing". Cold Spring Harbor Protocols 2010 (6): pdb.prot5448. June 2010. doi:10.1101/pdb.prot5448. PMID 20516186.  https://dx.doi.org/10.1101%2Fpdb.prot5448
  3. "Illumina Sequencing Technology". https://www.youtube.com/watch?v=womKfikWlxM. 
  4. "Parallel tagged amplicon sequencing of relatively long PCR products using the Illumina HiSeq platform and transcriptome assembly". Molecular Ecology Resources 16 (1): 91–102. January 2016. doi:10.1111/1755-0998.12429. PMID 25959587.  https://dx.doi.org/10.1111%2F1755-0998.12429
  5. Illumina, Inc.. "Multiplexed Sequencing with the Illumina Genome Analyzer System". http://www.illumina.com/documents/products/datasheets/datasheet_sequencing_multiplex.pdf. 
  6. "A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers". BMC Genomics 13: 341. July 2012. doi:10.1186/1471-2164-13-341. PMID 22827831.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3431227
  7. Clark, David P.; Pazdernik, Nanette J.; McGehee, Michelle R. (2019). Molecular Biology. Academic Cell. pp. 253–255. ISBN 9780128132883. 
  8. "Applications of next-generation sequencing technologies in functional genomics". Genomics 92 (5): 255–64. November 2008. doi:10.1016/j.ygeno.2008.07.001. PMID 18703132.  https://dx.doi.org/10.1016%2Fj.ygeno.2008.07.001
  9. "Improved pipeline for reducing erroneous identification by 16S rRNA sequences using the Illumina MiSeq platform". Journal of Microbiology 53 (1): 60–9. January 2015. doi:10.1007/s12275-015-4601-y. PMID 25557481.  https://dx.doi.org/10.1007%2Fs12275-015-4601-y
  10. "Generations of sequencing technologies". Genomics 93 (2): 105–11. February 2009. doi:10.1016/j.ygeno.2008.10.003. PMID 18992322.  https://dx.doi.org/10.1016%2Fj.ygeno.2008.10.003
  11. "De novo assembly and characterization of root transcriptome using Illumina paired-end sequencing and development of cSSR markers in sweet potato (Ipomoea batatas)". BMC Genomics 11: 726. December 2010. doi:10.1186/1471-2164-11-726. PMID 21182800.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3016421
  12. "The first insight into the tissue specific taxus transcriptome via Illumina second generation sequencing". PLOS ONE 6 (6): e21220. 22 June 2011. doi:10.1371/journal.pone.0021220. PMID 21731678. Bibcode: 2011PLoSO...621220H.  http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=3120849
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