DNA sequencer (English Wikipedia)

Cook-Deegan, Robert Mullan (1991). "Origins of the Human Genome Project". FASEB Journal. 5 (1). University of Washington: 8–11. doi:10.1096/fasebj.5.1.1991595. PMID 1991595. S2CID 37792736. Retrieved 20 October 2014.
Metzker, M. L. (2005). "Emerging technologies in DNA sequencing". Genome Res. 15 (12): 1767–1776. doi:10.1101/gr.3770505. PMID 16339375.
Hutchison, C. A. III. (2007). "DNA sequencing: bench to bedside and beyond". Nucleic Acids Res. 35 (18): 6227–6237. doi:10.1093/nar/gkm688. PMC 2094077. PMID 17855400.
F. S. Collins; M. Morgan; A. Patrinos (2003). "The Human Genome Project: lessons from large-scale biology". Science. 300 (5617): 286–290. Bibcode:2003Sci...300..286C. doi:10.1126/science.1084564. PMID 12690187. S2CID 22423746.
Quail, Michael A.; Smith, Miriam; Coupland, Paul; Otto, Thomas D.; Harris, Simon R.; Connor, Thomas R.; Bertoni, Anna; Swerdlow, Harold P.; Gu, Yong (2012-07-24). "A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers". BMC Genomics. 13 (1): 341. doi:10.1186/1471-2164-13-341. ISSN 1471-2164. PMC 3431227. PMID 22827831.
Michael A. Quail; Iwanka Kozarewa; Frances Smith; Aylwyn Scally; Philip J. Stephens; Richard Durbin; Harold Swerdlow; Daniel J. Turner (2008). "A large genome centre's improvements to the Illumina sequencing system". Nat Methods. 5 (12): 1005–1010. doi:10.1038/nmeth.1270. PMC 2610436. PMID 19034268.
Li, Heng; Ruan, Jue; Durbin, Richard (2008-11-01). "Mapping short DNA sequencing reads and calling variants using mapping quality scores". Genome Research. 18 (11): 1851–1858. doi:10.1101/gr.078212.108. ISSN 1088-9051. PMC 2577856. PMID 18714091.
Gilbert W, Maxam A (1973). "The Nucleotide Sequence of the lac Operator". Proc Natl Acad Sci U S A. 70 (12): 13581–3584. Bibcode:1973PNAS...70.3581G. doi:10.1073/pnas.70.12.3581. PMC 427284. PMID 4587255.
Sanger F, Coulson AR (May 1975). "A rapid method for determining sequences in DNA by primed synthesis with DNA polymerase". J. Mol. Biol. 94 (3): 441–8. doi:10.1016/0022-2836(75)90213-2. PMID 1100841.
Lin Liu; Yinhu Li; Siliang Li; Ni Hu; Yimin He; Ray Pong; Danni Lin; Lihua Lu; Maggie Law (2012). "Comparison of Next-Generation Sequencing Systems". Journal of Biomedicine and Biotechnology. 2012: 251364. doi:10.1155/2012/251364. PMC 3398667. PMID 22829749.
Mardis, Elaine R. (1 September 2008). "Next-Generation DNA Sequencing Methods". Annual Review of Genomics and Human Genetics. 9 (1): 387–402. doi:10.1146/annurev.genom.9.081307.164359. PMID 18576944. S2CID 2484571.
Rai, Alex J.; Kamath, Rashmi M.; Gerald, William; Fleisher, Martin (29 October 2008). "Analytical validation of the GeXP analyzer and design of a workflow for cancer-biomarker discovery using multiplexed gene-expression profiling". Analytical and Bioanalytical Chemistry. 393 (5): 1505–1511. doi:10.1007/s00216-008-2436-7. PMID 18958454. S2CID 46721686.
Koren, S; Schatz, MC; Walenz, BP; Martin, J; Howard, JT; Ganapathy, G; Wang, Z; Rasko, DA; McCombie, WR; Jarvis, ED; Phillippy, AM (Jul 1, 2012). "Hybrid error correction and de novo assembly of single-molecule sequencing reads". Nature Biotechnology. 30 (7): 693–700. doi:10.1038/nbt.2280. PMC 3707490. PMID 22750884.
Chin, Chen-Shan; Alexander, David H.; Marks, Patrick; Klammer, Aaron A.; Drake, James; Heiner, Cheryl; Clum, Alicia; Copeland, Alex; Huddleston, John; Eichler, Evan E.; Turner, Stephen W.; Korlach, Jonas (2013). "Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data". Nature Methods. 10 (6): 563–569. doi:10.1038/nmeth.2474. PMID 23644548. S2CID 205421576.
Tyler, Andrea D.; Mataseje, Laura; Urfano, Chantel J.; Schmidt, Lisa; Antonation, Kym S.; Mulvey, Michael R.; Corbett, Cindi R. (2018-07-19). "Evaluation of Oxford Nanopore's MinION Sequencing Device for Microbial Whole Genome Sequencing Applications". Scientific Reports. 8 (1): 10931. Bibcode:2018NatSR...810931T. doi:10.1038/s41598-018-29334-5. ISSN 2045-2322. PMC 6053456. PMID 30026559.
Jain, Miten; Koren, Sergey; Miga, Karen H.; Quick, Josh; Rand, Arthur C.; Sasani, Thomas A.; Tyson, John R.; Beggs, Andrew D.; Dilthey, Alexander T.; Fiddes, Ian T.; Malla, Sunir (29 January 2018). "Nanopore sequencing and assembly of a human genome with ultra-long reads". Nature Biotechnology. 36 (4): 338–345. doi:10.1038/nbt.4060. ISSN 1546-1696. PMC 5889714. PMID 29431738.
Lu, Hengyun; Giordano, Francesca; Ning, Zemin (2016-10-01). "Oxford Nanopore MinION Sequencing and Genome Assembly". Genomics, Proteomics & Bioinformatics. SI: Big Data and Precision Medicine. 14 (5): 265–279. doi:10.1016/j.gpb.2016.05.004. ISSN 1672-0229. PMC 5093776. PMID 27646134.
Kim, Hak-Min; Jeon, Sungwon; Chung, Oksung; Jun, Je Hoon; Kim, Hui-Su; Blazyte, Asta; Lee, Hwang-Yeol; Yu, Youngseok; Cho, Yun Sung; Bolser, Dan M; Bhak, Jong (2021-03-01). "Comparative analysis of 7 short-read sequencing platforms using the Korean Reference Genome: MGI and Illumina sequencing benchmark for whole-genome sequencing". GigaScience. 10 (3): giab014. doi:10.1093/gigascience/giab014. ISSN 2047-217X. PMC 7953489. PMID 33710328.
C Anukam, Kingsley; E Bassey, Bassey (2020). "Genetic Variants predisposition to Severe COVID-19 Illness Identified in a Healthy Nigerian Man, using Nebula Genomics Gene.iobio Platform" (PDF). Journal of Medical Laboratory Science. 30 (4): 62–75. doi:10.5281/zenodo.4399050. ISSN 1116-1043. S2CID 244988198.
Shen, Hanjie; Liu, Pengjuan; Li, Zhanqing; Chen, Fang; Jiang, Hui; Shi, Shiming; Xi, Yang; Li, Qiaoling; Wang, Xiaojue; Zhao, Jing; Liang, Xinming; Xie, Yinlong; Wang, Lin; Tian, Wenlan; Berntsen, Tam; Alexeev, Andrei; Luo, Yinling; Gong, Meihua; Li, Jiguang; Xu, Chongjun; Barua, Nina; Drmanac, Snezana; Dai, Sijie; Mi, Zilan; Ren, Han; Lin, Zhe; Chen, Ao; Zhang, Wenwei; Mu, Feng; Xu, Xun; Zhao, Xia; Jiang, Yuan; Drmanac, Radoje (23 December 2019). "Advanced Whole Genome Sequencing Using an Entirely PCR-free Massively Parallel Sequencing Workflow". bioRxiv 10.1101/2019.12.20.885517.
Liao, Mingfeng; Liu, Yang; Yuan, Jing; Wen, Yanling; Xu, Gang; Zhao, Juanjuan; Cheng, Lin; Li, Jinxiu; Wang, Xin; Wang, Fuxiang; Liu, Lei (May 12, 2020). "Single-cell landscape of bronchoalveolar immune cells in patients with COVID-19". Nature Medicine. 26 (6): 842–844. doi:10.1038/s41591-020-0901-9. ISSN 1546-170X. PMID 32398875. S2CID 218593518.
Shendure, J.; Ji, H. (2008). "Next-generation DNA sequencing". Nat. Biotechnol. 26 (10): 1135–1145. doi:10.1038/nbt1486. PMID 18846087. S2CID 6384349.
Sun, Xiaohuan; Wang, Jingjing; Fang, Chao; Li, Jiguang; Han, Mo; Wei, Xiaofang; Zheng, Haotian; Luo, Xiaoqing; Gong, Meihua; Xiao, Liang; Hu, Yuehua; Song, Zewei (2020-07-03). "Efficient and stable metabarcoding sequencing from DNBSEQ-G400 sequencer examined by large fungal community analysis". bioRxiv 10.1101/2020.07.02.185710.

engadget.com

"MinION USB-sized DNA sequencer goes through real-world testing". Engadget. 19 September 2014. Retrieved 2021-12-05.

genengnews.com

LeMieux, Julianna; PhD (2020-12-03). "Genomics Analysis Moves to the Next Level". GEN - Genetic Engineering and Biotechnology News. Retrieved 2021-12-20.

genomeweb.com

"Roche Shutting Down 454 Sequencing Business". GenomeWeb. 2013-10-15.
"PacBio Launches Higher-Throughput, Lower-Cost Single-Molecule Sequencing System". October 2015.
Karow, Julia (2010-03-02). "Ion Torrent Systems Presents $50,000 Electronic Sequencer at AGBT". GenomeWeb.

harvard.edu

ui.adsabs.harvard.edu

F. S. Collins; M. Morgan; A. Patrinos (2003). "The Human Genome Project: lessons from large-scale biology". Science. 300 (5617): 286–290. Bibcode:2003Sci...300..286C. doi:10.1126/science.1084564. PMID 12690187. S2CID 22423746.
Gilbert W, Maxam A (1973). "The Nucleotide Sequence of the lac Operator". Proc Natl Acad Sci U S A. 70 (12): 13581–3584. Bibcode:1973PNAS...70.3581G. doi:10.1073/pnas.70.12.3581. PMC 427284. PMID 4587255.
Tyler, Andrea D.; Mataseje, Laura; Urfano, Chantel J.; Schmidt, Lisa; Antonation, Kym S.; Mulvey, Michael R.; Corbett, Cindi R. (2018-07-19). "Evaluation of Oxford Nanopore's MinION Sequencing Device for Microbial Whole Genome Sequencing Applications". Scientific Reports. 8 (1): 10931. Bibcode:2018NatSR...810931T. doi:10.1038/s41598-018-29334-5. ISSN 2045-2322. PMC 6053456. PMID 30026559.

illumina.com

"Sequencing and Microarray Systems". www.illumina.com.

iontorrent.com

"Ion PGM - Ion Torrent". Archived from the original on 2012-09-20. Retrieved 2013-02-13.

jomls.org

C Anukam, Kingsley; E Bassey, Bassey (2020). "Genetic Variants predisposition to Severe COVID-19 Illness Identified in a Healthy Nigerian Man, using Nebula Genomics Gene.iobio Platform" (PDF). Journal of Medical Laboratory Science. 30 (4): 62–75. doi:10.5281/zenodo.4399050. ISSN 1116-1043. S2CID 244988198.

nasa.gov

Gaskill, Melissa (August 29, 2016). "First DNA Sequencing in Space a Game Changer". NASA. Retrieved October 26, 2016.

nih.gov

pubmed.ncbi.nlm.nih.gov

Cook-Deegan, Robert Mullan (1991). "Origins of the Human Genome Project". FASEB Journal. 5 (1). University of Washington: 8–11. doi:10.1096/fasebj.5.1.1991595. PMID 1991595. S2CID 37792736. Retrieved 20 October 2014.
Metzker, M. L. (2005). "Emerging technologies in DNA sequencing". Genome Res. 15 (12): 1767–1776. doi:10.1101/gr.3770505. PMID 16339375.
Hutchison, C. A. III. (2007). "DNA sequencing: bench to bedside and beyond". Nucleic Acids Res. 35 (18): 6227–6237. doi:10.1093/nar/gkm688. PMC 2094077. PMID 17855400.
F. S. Collins; M. Morgan; A. Patrinos (2003). "The Human Genome Project: lessons from large-scale biology". Science. 300 (5617): 286–290. Bibcode:2003Sci...300..286C. doi:10.1126/science.1084564. PMID 12690187. S2CID 22423746.
Quail, Michael A.; Smith, Miriam; Coupland, Paul; Otto, Thomas D.; Harris, Simon R.; Connor, Thomas R.; Bertoni, Anna; Swerdlow, Harold P.; Gu, Yong (2012-07-24). "A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers". BMC Genomics. 13 (1): 341. doi:10.1186/1471-2164-13-341. ISSN 1471-2164. PMC 3431227. PMID 22827831.
Michael A. Quail; Iwanka Kozarewa; Frances Smith; Aylwyn Scally; Philip J. Stephens; Richard Durbin; Harold Swerdlow; Daniel J. Turner (2008). "A large genome centre's improvements to the Illumina sequencing system". Nat Methods. 5 (12): 1005–1010. doi:10.1038/nmeth.1270. PMC 2610436. PMID 19034268.
Li, Heng; Ruan, Jue; Durbin, Richard (2008-11-01). "Mapping short DNA sequencing reads and calling variants using mapping quality scores". Genome Research. 18 (11): 1851–1858. doi:10.1101/gr.078212.108. ISSN 1088-9051. PMC 2577856. PMID 18714091.
Gilbert W, Maxam A (1973). "The Nucleotide Sequence of the lac Operator". Proc Natl Acad Sci U S A. 70 (12): 13581–3584. Bibcode:1973PNAS...70.3581G. doi:10.1073/pnas.70.12.3581. PMC 427284. PMID 4587255.
Sanger F, Coulson AR (May 1975). "A rapid method for determining sequences in DNA by primed synthesis with DNA polymerase". J. Mol. Biol. 94 (3): 441–8. doi:10.1016/0022-2836(75)90213-2. PMID 1100841.
Lin Liu; Yinhu Li; Siliang Li; Ni Hu; Yimin He; Ray Pong; Danni Lin; Lihua Lu; Maggie Law (2012). "Comparison of Next-Generation Sequencing Systems". Journal of Biomedicine and Biotechnology. 2012: 251364. doi:10.1155/2012/251364. PMC 3398667. PMID 22829749.
Mardis, Elaine R. (1 September 2008). "Next-Generation DNA Sequencing Methods". Annual Review of Genomics and Human Genetics. 9 (1): 387–402. doi:10.1146/annurev.genom.9.081307.164359. PMID 18576944. S2CID 2484571.
Rai, Alex J.; Kamath, Rashmi M.; Gerald, William; Fleisher, Martin (29 October 2008). "Analytical validation of the GeXP analyzer and design of a workflow for cancer-biomarker discovery using multiplexed gene-expression profiling". Analytical and Bioanalytical Chemistry. 393 (5): 1505–1511. doi:10.1007/s00216-008-2436-7. PMID 18958454. S2CID 46721686.
Koren, S; Schatz, MC; Walenz, BP; Martin, J; Howard, JT; Ganapathy, G; Wang, Z; Rasko, DA; McCombie, WR; Jarvis, ED; Phillippy, AM (Jul 1, 2012). "Hybrid error correction and de novo assembly of single-molecule sequencing reads". Nature Biotechnology. 30 (7): 693–700. doi:10.1038/nbt.2280. PMC 3707490. PMID 22750884.
Chin, Chen-Shan; Alexander, David H.; Marks, Patrick; Klammer, Aaron A.; Drake, James; Heiner, Cheryl; Clum, Alicia; Copeland, Alex; Huddleston, John; Eichler, Evan E.; Turner, Stephen W.; Korlach, Jonas (2013). "Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data". Nature Methods. 10 (6): 563–569. doi:10.1038/nmeth.2474. PMID 23644548. S2CID 205421576.
Tyler, Andrea D.; Mataseje, Laura; Urfano, Chantel J.; Schmidt, Lisa; Antonation, Kym S.; Mulvey, Michael R.; Corbett, Cindi R. (2018-07-19). "Evaluation of Oxford Nanopore's MinION Sequencing Device for Microbial Whole Genome Sequencing Applications". Scientific Reports. 8 (1): 10931. Bibcode:2018NatSR...810931T. doi:10.1038/s41598-018-29334-5. ISSN 2045-2322. PMC 6053456. PMID 30026559.
Jain, Miten; Koren, Sergey; Miga, Karen H.; Quick, Josh; Rand, Arthur C.; Sasani, Thomas A.; Tyson, John R.; Beggs, Andrew D.; Dilthey, Alexander T.; Fiddes, Ian T.; Malla, Sunir (29 January 2018). "Nanopore sequencing and assembly of a human genome with ultra-long reads". Nature Biotechnology. 36 (4): 338–345. doi:10.1038/nbt.4060. ISSN 1546-1696. PMC 5889714. PMID 29431738.
Lu, Hengyun; Giordano, Francesca; Ning, Zemin (2016-10-01). "Oxford Nanopore MinION Sequencing and Genome Assembly". Genomics, Proteomics & Bioinformatics. SI: Big Data and Precision Medicine. 14 (5): 265–279. doi:10.1016/j.gpb.2016.05.004. ISSN 1672-0229. PMC 5093776. PMID 27646134.
Kim, Hak-Min; Jeon, Sungwon; Chung, Oksung; Jun, Je Hoon; Kim, Hui-Su; Blazyte, Asta; Lee, Hwang-Yeol; Yu, Youngseok; Cho, Yun Sung; Bolser, Dan M; Bhak, Jong (2021-03-01). "Comparative analysis of 7 short-read sequencing platforms using the Korean Reference Genome: MGI and Illumina sequencing benchmark for whole-genome sequencing". GigaScience. 10 (3): giab014. doi:10.1093/gigascience/giab014. ISSN 2047-217X. PMC 7953489. PMID 33710328.
Liao, Mingfeng; Liu, Yang; Yuan, Jing; Wen, Yanling; Xu, Gang; Zhao, Juanjuan; Cheng, Lin; Li, Jinxiu; Wang, Xin; Wang, Fuxiang; Liu, Lei (May 12, 2020). "Single-cell landscape of bronchoalveolar immune cells in patients with COVID-19". Nature Medicine. 26 (6): 842–844. doi:10.1038/s41591-020-0901-9. ISSN 1546-170X. PMID 32398875. S2CID 218593518.
Shendure, J.; Ji, H. (2008). "Next-generation DNA sequencing". Nat. Biotechnol. 26 (10): 1135–1145. doi:10.1038/nbt1486. PMID 18846087. S2CID 6384349.

ncbi.nlm.nih.gov

Hutchison, C. A. III. (2007). "DNA sequencing: bench to bedside and beyond". Nucleic Acids Res. 35 (18): 6227–6237. doi:10.1093/nar/gkm688. PMC 2094077. PMID 17855400.
Quail, Michael A.; Smith, Miriam; Coupland, Paul; Otto, Thomas D.; Harris, Simon R.; Connor, Thomas R.; Bertoni, Anna; Swerdlow, Harold P.; Gu, Yong (2012-07-24). "A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers". BMC Genomics. 13 (1): 341. doi:10.1186/1471-2164-13-341. ISSN 1471-2164. PMC 3431227. PMID 22827831.
Michael A. Quail; Iwanka Kozarewa; Frances Smith; Aylwyn Scally; Philip J. Stephens; Richard Durbin; Harold Swerdlow; Daniel J. Turner (2008). "A large genome centre's improvements to the Illumina sequencing system". Nat Methods. 5 (12): 1005–1010. doi:10.1038/nmeth.1270. PMC 2610436. PMID 19034268.
Li, Heng; Ruan, Jue; Durbin, Richard (2008-11-01). "Mapping short DNA sequencing reads and calling variants using mapping quality scores". Genome Research. 18 (11): 1851–1858. doi:10.1101/gr.078212.108. ISSN 1088-9051. PMC 2577856. PMID 18714091.
Gilbert W, Maxam A (1973). "The Nucleotide Sequence of the lac Operator". Proc Natl Acad Sci U S A. 70 (12): 13581–3584. Bibcode:1973PNAS...70.3581G. doi:10.1073/pnas.70.12.3581. PMC 427284. PMID 4587255.
Lin Liu; Yinhu Li; Siliang Li; Ni Hu; Yimin He; Ray Pong; Danni Lin; Lihua Lu; Maggie Law (2012). "Comparison of Next-Generation Sequencing Systems". Journal of Biomedicine and Biotechnology. 2012: 251364. doi:10.1155/2012/251364. PMC 3398667. PMID 22829749.
Koren, S; Schatz, MC; Walenz, BP; Martin, J; Howard, JT; Ganapathy, G; Wang, Z; Rasko, DA; McCombie, WR; Jarvis, ED; Phillippy, AM (Jul 1, 2012). "Hybrid error correction and de novo assembly of single-molecule sequencing reads". Nature Biotechnology. 30 (7): 693–700. doi:10.1038/nbt.2280. PMC 3707490. PMID 22750884.
Tyler, Andrea D.; Mataseje, Laura; Urfano, Chantel J.; Schmidt, Lisa; Antonation, Kym S.; Mulvey, Michael R.; Corbett, Cindi R. (2018-07-19). "Evaluation of Oxford Nanopore's MinION Sequencing Device for Microbial Whole Genome Sequencing Applications". Scientific Reports. 8 (1): 10931. Bibcode:2018NatSR...810931T. doi:10.1038/s41598-018-29334-5. ISSN 2045-2322. PMC 6053456. PMID 30026559.
Jain, Miten; Koren, Sergey; Miga, Karen H.; Quick, Josh; Rand, Arthur C.; Sasani, Thomas A.; Tyson, John R.; Beggs, Andrew D.; Dilthey, Alexander T.; Fiddes, Ian T.; Malla, Sunir (29 January 2018). "Nanopore sequencing and assembly of a human genome with ultra-long reads". Nature Biotechnology. 36 (4): 338–345. doi:10.1038/nbt.4060. ISSN 1546-1696. PMC 5889714. PMID 29431738.
Lu, Hengyun; Giordano, Francesca; Ning, Zemin (2016-10-01). "Oxford Nanopore MinION Sequencing and Genome Assembly". Genomics, Proteomics & Bioinformatics. SI: Big Data and Precision Medicine. 14 (5): 265–279. doi:10.1016/j.gpb.2016.05.004. ISSN 1672-0229. PMC 5093776. PMID 27646134.
Kim, Hak-Min; Jeon, Sungwon; Chung, Oksung; Jun, Je Hoon; Kim, Hui-Su; Blazyte, Asta; Lee, Hwang-Yeol; Yu, Youngseok; Cho, Yun Sung; Bolser, Dan M; Bhak, Jong (2021-03-01). "Comparative analysis of 7 short-read sequencing platforms using the Korean Reference Genome: MGI and Illumina sequencing benchmark for whole-genome sequencing". GigaScience. 10 (3): giab014. doi:10.1093/gigascience/giab014. ISSN 2047-217X. PMC 7953489. PMID 33710328.

otago.ac.nz

sequence.otago.ac.nz

Genome Sequencer FLX System Software Manual, version 2.3

pacb.com

"PacBio Sequel Systems".
"Home - PacBio - Sequence with Confidence". PacBio.

sciencedaily.com

"New method helps pocket-sized DNA sequencer achieve near-perfect accuracy". ScienceDaily. Retrieved 2021-12-05.

semanticscholar.org

api.semanticscholar.org

Cook-Deegan, Robert Mullan (1991). "Origins of the Human Genome Project". FASEB Journal. 5 (1). University of Washington: 8–11. doi:10.1096/fasebj.5.1.1991595. PMID 1991595. S2CID 37792736. Retrieved 20 October 2014.
F. S. Collins; M. Morgan; A. Patrinos (2003). "The Human Genome Project: lessons from large-scale biology". Science. 300 (5617): 286–290. Bibcode:2003Sci...300..286C. doi:10.1126/science.1084564. PMID 12690187. S2CID 22423746.
Mardis, Elaine R. (1 September 2008). "Next-Generation DNA Sequencing Methods". Annual Review of Genomics and Human Genetics. 9 (1): 387–402. doi:10.1146/annurev.genom.9.081307.164359. PMID 18576944. S2CID 2484571.
Rai, Alex J.; Kamath, Rashmi M.; Gerald, William; Fleisher, Martin (29 October 2008). "Analytical validation of the GeXP analyzer and design of a workflow for cancer-biomarker discovery using multiplexed gene-expression profiling". Analytical and Bioanalytical Chemistry. 393 (5): 1505–1511. doi:10.1007/s00216-008-2436-7. PMID 18958454. S2CID 46721686.
Chin, Chen-Shan; Alexander, David H.; Marks, Patrick; Klammer, Aaron A.; Drake, James; Heiner, Cheryl; Clum, Alicia; Copeland, Alex; Huddleston, John; Eichler, Evan E.; Turner, Stephen W.; Korlach, Jonas (2013). "Nonhybrid, finished microbial genome assemblies from long-read SMRT sequencing data". Nature Methods. 10 (6): 563–569. doi:10.1038/nmeth.2474. PMID 23644548. S2CID 205421576.
C Anukam, Kingsley; E Bassey, Bassey (2020). "Genetic Variants predisposition to Severe COVID-19 Illness Identified in a Healthy Nigerian Man, using Nebula Genomics Gene.iobio Platform" (PDF). Journal of Medical Laboratory Science. 30 (4): 62–75. doi:10.5281/zenodo.4399050. ISSN 1116-1043. S2CID 244988198.
Liao, Mingfeng; Liu, Yang; Yuan, Jing; Wen, Yanling; Xu, Gang; Zhao, Juanjuan; Cheng, Lin; Li, Jinxiu; Wang, Xin; Wang, Fuxiang; Liu, Lei (May 12, 2020). "Single-cell landscape of bronchoalveolar immune cells in patients with COVID-19". Nature Medicine. 26 (6): 842–844. doi:10.1038/s41591-020-0901-9. ISSN 1546-170X. PMID 32398875. S2CID 218593518.
Shendure, J.; Ji, H. (2008). "Next-generation DNA sequencing". Nat. Biotechnol. 26 (10): 1135–1145. doi:10.1038/nbt1486. PMID 18846087. S2CID 6384349.

technologyreview.com

Regalado, Antonio (September 17, 2014). "Radical New DNA Sequencer Finally Gets into Researchers' Hands". Technology Review. Retrieved October 3, 2014.

thermofisher.com

"Applied Biosystems - US". www.thermofisher.com.
"Sanger Sequencing and Fragment Analysis by CE - US". www.thermofisher.com.
"Ion Torrent".
"Applied Biosystems SeqStudio Genetic Analyzer - US".
"Applied Biosystems - US". www.thermofisher.com.
"Sequencing - US". www.thermofisher.com.

washington.edu

faculty.washington.edu

Cook-Deegan, Robert Mullan (1991). "Origins of the Human Genome Project". FASEB Journal. 5 (1). University of Washington: 8–11. doi:10.1096/fasebj.5.1.1991595. PMID 1991595. S2CID 37792736. Retrieved 20 October 2014.

web.archive.org

"Products : 454 Life Sciences, a Roche Company". Archived from the original on 2012-09-13. Retrieved 2012-09-05.
"Products - GS FLX+ System : 454 Life Sciences, a Roche Company". Archived from the original on 2012-09-05. Retrieved 2012-09-05.
"Products - GS Junior System : 454 Life Sciences, a Roche Company". Archived from the original on 2012-09-13. Retrieved 2012-09-05.
"Products - Analysis Software : 454 Life Science, a Roche Company". Archived from the original on 2009-02-19. Retrieved 2013-10-23.
"GenomeLab GeXP manual" (PDF). Medgar Evers College, City University of New York. August 2014. Archived (PDF) from the original on 2021-12-05.
"Ion PGM - Ion Torrent". Archived from the original on 2012-09-20. Retrieved 2013-02-13.

worldcat.org

search.worldcat.org

Quail, Michael A.; Smith, Miriam; Coupland, Paul; Otto, Thomas D.; Harris, Simon R.; Connor, Thomas R.; Bertoni, Anna; Swerdlow, Harold P.; Gu, Yong (2012-07-24). "A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers". BMC Genomics. 13 (1): 341. doi:10.1186/1471-2164-13-341. ISSN 1471-2164. PMC 3431227. PMID 22827831.
Li, Heng; Ruan, Jue; Durbin, Richard (2008-11-01). "Mapping short DNA sequencing reads and calling variants using mapping quality scores". Genome Research. 18 (11): 1851–1858. doi:10.1101/gr.078212.108. ISSN 1088-9051. PMC 2577856. PMID 18714091.
Tyler, Andrea D.; Mataseje, Laura; Urfano, Chantel J.; Schmidt, Lisa; Antonation, Kym S.; Mulvey, Michael R.; Corbett, Cindi R. (2018-07-19). "Evaluation of Oxford Nanopore's MinION Sequencing Device for Microbial Whole Genome Sequencing Applications". Scientific Reports. 8 (1): 10931. Bibcode:2018NatSR...810931T. doi:10.1038/s41598-018-29334-5. ISSN 2045-2322. PMC 6053456. PMID 30026559.
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