These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
155 related articles for article (PubMed ID: 29621212)
1. The long view on sequencing. Nat Biotechnol; 2018 Apr; 36(4):287. PubMed ID: 29621212 [No Abstract] [Full Text] [Related]
2. Advancements in Next-Generation Sequencing. Levy SE; Myers RM Annu Rev Genomics Hum Genet; 2016 Aug; 17():95-115. PubMed ID: 27362342 [TBL] [Abstract][Full Text] [Related]
3. WHEN TWO IS BETTER THAN ONE. Perkel J Biotechniques; 2016 Feb; 60(2):56-60. PubMed ID: 26842349 [TBL] [Abstract][Full Text] [Related]
4. Three decades of nanopore sequencing. Deamer D; Akeson M; Branton D Nat Biotechnol; 2016 May; 34(5):518-24. PubMed ID: 27153285 [TBL] [Abstract][Full Text] [Related]
5. Future Promises and Concerns of Ubiquitous Next-Generation Sequencing. McCombie WR; McPherson JD Cold Spring Harb Perspect Med; 2019 Sep; 9(9):. PubMed ID: 30478095 [TBL] [Abstract][Full Text] [Related]
6. [New generation sequencing in medical genetics]. Stoppa-Lyonnet D; Houdayer C Med Sci (Paris); 2012 Feb; 28(2):123-4. PubMed ID: 22377291 [No Abstract] [Full Text] [Related]
7. Closing in on a complete human genome. Eisenstein M Nature; 2021 Feb; 590(7847):679-681. PubMed ID: 33619406 [No Abstract] [Full Text] [Related]
8. The current state of clinical interpretation of sequence variants. Hoskinson DC; Dubuc AM; Mason-Suares H Curr Opin Genet Dev; 2017 Feb; 42():33-39. PubMed ID: 28157586 [TBL] [Abstract][Full Text] [Related]
9. Super-speedy sequencing puts genomic diagnosis in the fast lane. Eisenstein M Nature; 2024 Feb; 626(8000):915-917. PubMed ID: 38374432 [No Abstract] [Full Text] [Related]
10. The Impact of Next-Generation Sequencing on Cancer Genomics: From Discovery to Clinic. Mardis ER Cold Spring Harb Perspect Med; 2019 Sep; 9(9):. PubMed ID: 30397020 [TBL] [Abstract][Full Text] [Related]
11. Next-Generation Sequencing Strategies. Levy SE; Boone BE Cold Spring Harb Perspect Med; 2019 Jul; 9(7):. PubMed ID: 30323017 [TBL] [Abstract][Full Text] [Related]
12. Why Deep Learning Is Changing the Way to Approach NGS Data Processing: A Review. Celesti F; Celesti A; Wan J; Villari M IEEE Rev Biomed Eng; 2018; 11():68-76. PubMed ID: 29993643 [TBL] [Abstract][Full Text] [Related]
13. Making pretest genomic counseling optional: lessons from the RAVE study. Sutton EJ; Kullo IJ; Sharp RR Genet Med; 2018 Oct; 20(10):1157-1158. PubMed ID: 29388941 [No Abstract] [Full Text] [Related]
14. Genomics: the personal side of genomics. Blow N Nature; 2007 Oct; 449(7162):627-30. PubMed ID: 17914399 [No Abstract] [Full Text] [Related]
15. [DNA sequencing by nanopores: achievements and prospects]. Montel F Med Sci (Paris); 2018 Feb; 34(2):161-165. PubMed ID: 29451487 [TBL] [Abstract][Full Text] [Related]
16. From Sanger sequencing to genome databases and beyond. Straiton J; Free T; Sawyer A; Martin J Biotechniques; 2019 Feb; 66(2):60-63. PubMed ID: 30744413 [TBL] [Abstract][Full Text] [Related]
17. Deep learning of genomic variation and regulatory network data. Telenti A; Lippert C; Chang PC; DePristo M Hum Mol Genet; 2018 May; 27(R1):R63-R71. PubMed ID: 29648622 [TBL] [Abstract][Full Text] [Related]