Review
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New generation genome sequencing methods

Year 2022, Volume: 6 Issue: 4, 503 - 506, 01.04.2022

Ilgın Kekeç Nisa Sipahi Serkan İkiz

https://doi.org/10.28982/josam.972535

Abstract

Sequencing procedures, which present information related to events in the living metabolism, are performed by genetic methods. Gene structure and genetic control mechanisms can be determined by sequencing methods, as they represent significant contributions to transcriptomic, ecological, and epidemiological studies. Thus, chromosomal abnormalities in living things with a whole genome analysis of different organisms (e.g., plants, bacteria, yeast, fungi, and viruses) are detected quickly, so that clinical disease can be diagnosed with reliable data from biomedical research. The nucleic acid sequencing processes have a history of about fifty years. With the technology developed in recent years, second and third-generation methods, known as next-generation sequencing (NGS), found their rightful place in the sector approximately 15 years ago. New-generation sequencing promotes inexpensive, routine, and comprehensive analyses of the living genome. In general, sequencing methods are separated as first-, second-, and third-generation sequencing methods, with the latter called ‘new-generation sequencing:’ our review focuses on these specific sequencing methods.

Keywords

DNA Genome New generation sequencing Sequencing methods

References

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  • 28. Hestand MS, Ameur A. The versatility of SMRT sequencing. Genes. 2019;10(1):24. doi: 10.3390/genes10010024.
  • 29. Ameur A, Che H, Martin M, Bunikis I, Dahlberg J, Hoijer I, et al. De novo assembly of two Swedish genomes reveals missing segments from the human GRCh38 reference and improves variant calling of population-scale sequencing data. Genes. 2018;9(10):486. doi: 10.3390/genes9100486
  • 30. Laehnemann D, Borkhardt A, McHardy AC. Denoising DNA deep sequencing data high-throughput sequencing errors and their correction. Brief Bioinformatics. 2015;17(1):154-79.
  • 31. Jain M, Hugh EO, Paten B, Akeson M. The oxford nanopore MinION: Delivery of nanopore sequencing to the genomics community. Genome Biol. 2016;17(1):1-11.
  • 32. Lu H, Giordano F, Ning Z. Oxford nanopore MinION sequencing and genome assembly. Genomics Proteomics Bioinformatics. 2016;14(1):265-79.
  • 33. Laver T, Harrison J, O’Neill PA, Moore K, Farbos A, Paszkiewicz K, Studholme DJ. Assessing the performance of the Oxford Nanopore Technologies MinION. Biomol Detect Quantif. 2015;3:1–8. doi: 10.1016/j.bdq.2015.02.001.

Year 2022, Volume: 6 Issue: 4, 503 - 506, 01.04.2022

Ilgın Kekeç Nisa Sipahi Serkan İkiz

https://doi.org/10.28982/josam.972535

Abstract

References

  • 1. Kizmaz MZ, Paylan İC, and Erkan S. Historical development of DNA sequencing. Gaziosmanpaşa University Gbad. 2017;6(2):47-53.
  • 2. Darcan C, Türkyılmaz O. Overview of next generation sequencing technology. Bilecik Şeyh Edebali University J of Sci. 2018;5(1):41–9.
  • 3. McCombie WR, McPherson JD, Mardis ER. Next generation sequencing technologies. Cold Spring Harb Perspect Med. 2019;9(11):a036798.
  • 4. Ustek D, Abaci N, Sirma S, Cakiris A. New generation DNA sequencing. Experimed. 2011;1(1):11–8.
  • 5. Akyol İ, Yildiz MA, Tutar E. Yeni nesil nükleotid dizileme metotlarının biyokimyasal temelleri. Tarim ve Doga Dergisi. 2017;20(1):1-15.
  • 6. Liu L, Li Y, Li S, Hu N, He Y, Pong R, et al. Comparison of next-generation sequencing systems. J Biomed Biotechnol. 2012;2012:1-11. doi: 10.1155/2012/251364.
  • 7. Kamps R, Brandão RD, Bosh BJ van den, Paulussen ADC, Xanthoulea S, Blok MJ, et al. Next-Generation sequencing in oncology : Genetic diagnosis, risk prediction and cancer classification. Int. J. Mol. Sci. 2017;18(2):308. doi: 10.3390/ijms18020308.
  • 8. Dogan M, Eroz R, Yuce H, Ozmerdivenli R. The known about next-generation sequencing (NGS). Duzce Med J. 2017;19(1):27–30.
  • 9. Kchouk M, Gibrat J, Elloumi M. Generations of sequencing technologies: from first to next generation. Biol Med. 2017;9(3):1-8. doi: 10.4172/0974-8369.1000395
  • 10. Bruijns B, Tiggelaar R, Gardeniers H. Massively parallel sequencing techniques for forensics: a review. Electrophoresis. 2018;39(21):2642-54.
  • 11. Kanagal-Shamanna R. Emulsion PCR. Techniques and Applications. Clinical applications of PCR. Humana Press, New York, NY. 2016;1392:33-42.
  • 12. Verma V, Gupta A, Chaudhary VK. Emulsion PCR made easy. BioTechniques. 2020;69(1):64-9.
  • 13. Callahan BJ, McMurdie PJ, Rosen MJ, Han AW, Johnson AJA, Holmes SP. DADA2: high-resolution sample inference from Illumina amplicon data. Nat Methods. 2016;13(7):581-3.
  • 14. Melamede RJ. U.S. Patent No. 4,863,849. Washington, DC: U.S. Patent and Trademark Office. 1989
  • 15. Luo C, Tsementzi D, Kyrpides N, Read T, Konstantinidis KT. Direct comparisons of Illumina vs. Roche 454 sequencing technologies on the same microbial community DNA sample. PloS One. 2012;7(2):1-12.
  • 16. White RA, Callister SJ, Moore RJ, Baker ES, Jansson JK. The past, present and future of microbiome analyses. Nat Protocols. 2016;11(11):2049-53.
  • 17. Manley LJ, Ma D, Levine SS. Monitoring error rates in Illumina sequencing. Journal of biomolecular techniques: JBT. 2016;27(4):125.
  • 18. Schirmer M, D’Amore R, Ijaz UZ, Hall N, Quince C. Illumina error profiles: resolving fine-scale variation in metagenomic sequencing data. BMC Bioinformatics. 2016;17(1):1-15.
  • 19. Song L, Huang W, Kang J, Huang Y, Ren H, Ding K. Comparison of error correction algorithms for Ion Torrent PGM data: application to hepatitis B virus. Sci Rep. 2017;7(1):1-11.
  • 20. Adamiak J, Otlewska A, Tafer H, Lopandic K, Gutarowska B, Sterflinger K, Piñar G. First evaluation of the microbiome of built cultural heritage by using the Ion Torrent next generation sequencing platform. Int Biodeter Biodegradation. 2018;131:11-8.
  • 21. Guerrero-Sanchez VM, Maldonado-Alconada AM, Amil-Ruiz F, Verardi A, Jorrín-Novo JV, Rey MD. Ion Torrent and lllumina, two complementary RNA-seq platforms for constructing the holm oak (Quercus ilex) transcriptome. PLoS One. 2019;14(1):1-18.
  • 22. Ambardar S, Gupta R, Trakroo D, Lal R, Vakhlu J. High throughput sequencing: an overview of sequencing chemistry. Indian J Microbiol. 2016;56(4):394-404.
  • 23. Hayden EC. Nanopore genome sequencer makes its debut. Nat News. 2012. doi: 10.1038/nature.2012.10051.
  • 24. Lee H, Gurtowski J, Yoo S, Nattestad M, Marcus S, Goodwin S, et al. Third-generation sequencing and the future of genomics. BioRxiv. 2016;1-20. doi: 10.1101/048603.
  • 25. Thompson JF, Steinmann KE. Single molecule sequencing with a HeliScope genetic analysis system. Curr Protoc Mol Biol. 2010;92(1):7-10.
  • 26. Ardui S, Ameur A, Vermeesch JR, Hestand MS. Single Molecule Real-Time (SMRT) Sequencing Comes of Age: Applications and utilities for medical diagnostics. Nucleic Acids Res. 2018;46(5):2159–68.
  • 27. Hart C, Lipson D, Ozsolak F, Raz T, Steinmann K, Thompson J, Milos PM. Single molecule sequencing:sequence method to enable accurate quantitation. Methods Enzymol. 2010;472:407–30. doi: 10.1016/S0076-6879(10)72002-4.
  • 28. Hestand MS, Ameur A. The versatility of SMRT sequencing. Genes. 2019;10(1):24. doi: 10.3390/genes10010024.
  • 29. Ameur A, Che H, Martin M, Bunikis I, Dahlberg J, Hoijer I, et al. De novo assembly of two Swedish genomes reveals missing segments from the human GRCh38 reference and improves variant calling of population-scale sequencing data. Genes. 2018;9(10):486. doi: 10.3390/genes9100486
  • 30. Laehnemann D, Borkhardt A, McHardy AC. Denoising DNA deep sequencing data high-throughput sequencing errors and their correction. Brief Bioinformatics. 2015;17(1):154-79.
  • 31. Jain M, Hugh EO, Paten B, Akeson M. The oxford nanopore MinION: Delivery of nanopore sequencing to the genomics community. Genome Biol. 2016;17(1):1-11.
  • 32. Lu H, Giordano F, Ning Z. Oxford nanopore MinION sequencing and genome assembly. Genomics Proteomics Bioinformatics. 2016;14(1):265-79.
  • 33. Laver T, Harrison J, O’Neill PA, Moore K, Farbos A, Paszkiewicz K, Studholme DJ. Assessing the performance of the Oxford Nanopore Technologies MinION. Biomol Detect Quantif. 2015;3:1–8. doi: 10.1016/j.bdq.2015.02.001.
There are 33 citations in total.

Details

Primary Language English
Subjects Biochemistry and Cell Biology (Other), Medical Microbiology
Journal Section Review
Authors

Ilgın Kekeç 0000-0002-0821-8376

Nisa Sipahi 0000-0001-8915-3545

Serkan İkiz 0000-0001-6502-0780

Publication Date April 1, 2022
Published in Issue Year 2022 Volume: 6 Issue: 4

Cite

APA Kekeç, I., Sipahi, N., & İkiz, S. (2022). New generation genome sequencing methods. Journal of Surgery and Medicine, 6(4), 503-506. https://doi.org/10.28982/josam.972535
AMA Kekeç I, Sipahi N, İkiz S. New generation genome sequencing methods. J Surg Med. April 2022;6(4):503-506. doi:10.28982/josam.972535
Chicago Kekeç, Ilgın, Nisa Sipahi, and Serkan İkiz. “New Generation Genome Sequencing Methods”. Journal of Surgery and Medicine 6, no. 4 (April 2022): 503-6. https://doi.org/10.28982/josam.972535.
EndNote Kekeç I, Sipahi N, İkiz S (April 1, 2022) New generation genome sequencing methods. Journal of Surgery and Medicine 6 4 503–506.
IEEE I. Kekeç, N. Sipahi, and S. İkiz, “New generation genome sequencing methods”, J Surg Med, vol. 6, no. 4, pp. 503–506, 2022, doi: 10.28982/josam.972535.
ISNAD Kekeç, Ilgın et al. “New Generation Genome Sequencing Methods”. Journal of Surgery and Medicine 6/4 (April 2022), 503-506. https://doi.org/10.28982/josam.972535.
JAMA Kekeç I, Sipahi N, İkiz S. New generation genome sequencing methods. J Surg Med. 2022;6:503–506.
MLA Kekeç, Ilgın et al. “New Generation Genome Sequencing Methods”. Journal of Surgery and Medicine, vol. 6, no. 4, 2022, pp. 503-6, doi:10.28982/josam.972535.
Vancouver Kekeç I, Sipahi N, İkiz S. New generation genome sequencing methods. J Surg Med. 2022;6(4):503-6.
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