Sanger sequencing (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Sanger sequencing" in English language version.

refsWebsite

Global rank English rank

29nih.gov

4^th place

19doi.org

2^nd place

3harvard.edu

18^th place

17^th place

3worldcat.org

5^th place

3semanticscholar.org

11^th place

8^th place

1nytimes.com

7^th place

1phrap.com

low place

1microchipbiotech.com

low place

doi.org

Chait, Edward; Page, Guy; Hunkapiller, Michael (1988). "Battle of the DNA sequencers". Nature. 333 (6172): 477–478. Bibcode:1988Natur.333..477C. doi:10.1038/333477a0. ISSN 0028-0836.
Zhang, J (1999-12-15). "A multiple-capillary electrophoresis system for small-scale DNA sequencing and analysis". Nucleic Acids Research. 27 (24): 36e–36. doi:10.1093/nar/27.24.e36. PMC 148759. PMID 10572188.
Shendure J, Ji H (October 2008). "Next-generation DNA sequencing". Nature Biotechnology. 26 (10): 1135–1145. doi:10.1038/nbt1486. PMID 18846087. S2CID 6384349.
Daniels RS, Harvey R, Ermetal B, Xiang Z, Galiano M, Adams L, McCauley JW (November 2021). "A Sanger sequencing protocol for SARS-CoV-2 S-gene". Influenza and Other Respiratory Viruses. 15 (6): 707–710. doi:10.1111/irv.12892. PMC 8447197. PMID 34346163.
Vega E, Barclay L, Gregoricus N, Williams K, Lee D, Vinjé J (August 2011). "Novel surveillance network for norovirus gastroenteritis outbreaks, United States". Emerging Infectious Diseases. 17 (8): 1389–1395. doi:10.3201/eid1708.101837. PMC 3381557. PMID 21801614.
Sanger F, Nicklen S, Coulson AR (December 1977). "DNA sequencing with chain-terminating inhibitors". Proceedings of the National Academy of Sciences of the United States of America. 74 (12): 5463–5467. Bibcode:1977PNAS...74.5463S. doi:10.1073/pnas.74.12.5463. PMC 431765. PMID 271968.
Smith LM, Sanders JZ, Kaiser RJ, Hughes P, Dodd C, Connell CR, et al. (1986). "Fluorescence detection in automated DNA sequence analysis". Nature. 321 (6071): 674–679. Bibcode:1986Natur.321..674S. doi:10.1038/321674a0. PMID 3713851. S2CID 27800972. We have developed a method for the partial automation of DNA sequence analysis. Fluorescence detection of the DNA fragments is accomplished by means of a fluorophore covalently attached to the oligonucleotide primer used in enzymatic DNA sequence analysis. A different coloured fluorophore is used for each of the reactions specific for the bases A, C, G and T. The reaction mixtures are combined and co-electrophoresed down a single polyacrylamide gel tube, the separated fluorescent bands of DNA are detected near the bottom of the tube, and the sequence information is acquired directly by computer.
Smith LM, Fung S, Hunkapiller MW, Hunkapiller TJ, Hood LE (April 1985). "The synthesis of oligonucleotides containing an aliphatic amino group at the 5' terminus: synthesis of fluorescent DNA primers for use in DNA sequence analysis". Nucleic Acids Research. 13 (7): 2399–2412. doi:10.1093/nar/13.7.2399. PMC 341163. PMID 4000959.
Crossley, Beate M.; Bai, Jianfa; Glaser, Amy; Maes, Roger; Porter, Elizabeth; Killian, Mary Lea; Clement, Travis; Toohey-Kurth, Kathy (November 2020). "Guidelines for Sanger sequencing and molecular assay monitoring". Journal of Veterinary Diagnostic Investigation. 32 (6): 767–775. doi:10.1177/1040638720905833. ISSN 1040-6387. PMC 7649556. PMID 32070230.
Sanches PR, Charlie-Silva I, Braz HL, Bittar C, Freitas Calmon M, Rahal P, Cilli EM (September 2021). "Recent advances in SARS-CoV-2 Spike protein and RBD mutations comparison between new variants Alpha (B.1.1.7, United Kingdom), Beta (B.1.351, South Africa), Gamma (P.1, Brazil) and Delta (B.1.617.2, India)". Journal of Virus Eradication. 7 (3): 100054. doi:10.1016/j.jve.2021.100054. PMC 8443533. PMID 34548928.
Ledergerber C, Dessimoz C (September 2011). "Base-calling for next-generation sequencing platforms". Briefings in Bioinformatics. 12 (5): 489–497. doi:10.1093/bib/bbq077. PMC 3178052. PMID 21245079.
Murphy KM, Berg KD, Eshleman JR (January 2005). "Sequencing of genomic DNA by combined amplification and cycle sequencing reaction". Clinical Chemistry. 51 (1): 35–39. doi:10.1373/clinchem.2004.039164. PMID 15514094.
SenGupta DJ, Cookson BT (May 2010). "SeqSharp: A general approach for improving cycle-sequencing that facilitates a robust one-step combined amplification and sequencing method". The Journal of Molecular Diagnostics. 12 (3): 272–277. doi:10.2353/jmoldx.2010.090134. PMC 2860461. PMID 20203000.
Kan CW, Fredlake CP, Doherty EA, Barron AE (November 2004). "DNA sequencing and genotyping in miniaturized electrophoresis systems". Electrophoresis. 25 (21–22): 3564–3588. doi:10.1002/elps.200406161. PMID 15565709. S2CID 4851728.
Morozova O, Marra MA (November 2008). "Applications of next-generation sequencing technologies in functional genomics". Genomics. 92 (5): 255–264. doi:10.1016/j.ygeno.2008.07.001. PMID 18703132.
Sinville R, Soper SA (July 2007). "High resolution DNA separations using microchip electrophoresis". Journal of Separation Science. 30 (11): 1714–1728. doi:10.1002/jssc.200700150. PMID 17623451.
Kumar KR, Cowley MJ, Davis RL (October 2019). "Next-Generation Sequencing and Emerging Technologies". Seminars in Thrombosis and Hemostasis. 45 (7): 661–673. doi:10.1055/s-0039-1688446. PMID 31096307.
Mastrorosa FK, Miller DE, Eichler EE (June 2023). "Applications of long-read sequencing to Mendelian genetics". Genome Medicine. 15 (1): 42. doi:10.1186/s13073-023-01194-3. PMC 10266321. PMID 37316925.
Tyson JR, O'Neil NJ, Jain M, Olsen HE, Hieter P, Snutch TP (February 2018). "MinION-based long-read sequencing and assembly extends the Caenorhabditis elegans reference genome". Genome Research. 28 (2): 266–274. doi:10.1101/gr.221184.117. PMC 5793790. PMID 29273626.

harvard.edu

ui.adsabs.harvard.edu

Chait, Edward; Page, Guy; Hunkapiller, Michael (1988). "Battle of the DNA sequencers". Nature. 333 (6172): 477–478. Bibcode:1988Natur.333..477C. doi:10.1038/333477a0. ISSN 0028-0836.
Sanger F, Nicklen S, Coulson AR (December 1977). "DNA sequencing with chain-terminating inhibitors". Proceedings of the National Academy of Sciences of the United States of America. 74 (12): 5463–5467. Bibcode:1977PNAS...74.5463S. doi:10.1073/pnas.74.12.5463. PMC 431765. PMID 271968.
Smith LM, Sanders JZ, Kaiser RJ, Hughes P, Dodd C, Connell CR, et al. (1986). "Fluorescence detection in automated DNA sequence analysis". Nature. 321 (6071): 674–679. Bibcode:1986Natur.321..674S. doi:10.1038/321674a0. PMID 3713851. S2CID 27800972. We have developed a method for the partial automation of DNA sequence analysis. Fluorescence detection of the DNA fragments is accomplished by means of a fluorophore covalently attached to the oligonucleotide primer used in enzymatic DNA sequence analysis. A different coloured fluorophore is used for each of the reactions specific for the bases A, C, G and T. The reaction mixtures are combined and co-electrophoresed down a single polyacrylamide gel tube, the separated fluorescent bands of DNA are detected near the bottom of the tube, and the sequence information is acquired directly by computer.

microchipbiotech.com

Microchip Biologies Inc. Apollo 100

nih.gov

pubmed.ncbi.nlm.nih.gov

Zhang, J (1999-12-15). "A multiple-capillary electrophoresis system for small-scale DNA sequencing and analysis". Nucleic Acids Research. 27 (24): 36e–36. doi:10.1093/nar/27.24.e36. PMC 148759. PMID 10572188.
Shendure J, Ji H (October 2008). "Next-generation DNA sequencing". Nature Biotechnology. 26 (10): 1135–1145. doi:10.1038/nbt1486. PMID 18846087. S2CID 6384349.
Daniels RS, Harvey R, Ermetal B, Xiang Z, Galiano M, Adams L, McCauley JW (November 2021). "A Sanger sequencing protocol for SARS-CoV-2 S-gene". Influenza and Other Respiratory Viruses. 15 (6): 707–710. doi:10.1111/irv.12892. PMC 8447197. PMID 34346163.
Vega E, Barclay L, Gregoricus N, Williams K, Lee D, Vinjé J (August 2011). "Novel surveillance network for norovirus gastroenteritis outbreaks, United States". Emerging Infectious Diseases. 17 (8): 1389–1395. doi:10.3201/eid1708.101837. PMC 3381557. PMID 21801614.
Sanger F, Nicklen S, Coulson AR (December 1977). "DNA sequencing with chain-terminating inhibitors". Proceedings of the National Academy of Sciences of the United States of America. 74 (12): 5463–5467. Bibcode:1977PNAS...74.5463S. doi:10.1073/pnas.74.12.5463. PMC 431765. PMID 271968.
Smith LM, Sanders JZ, Kaiser RJ, Hughes P, Dodd C, Connell CR, et al. (1986). "Fluorescence detection in automated DNA sequence analysis". Nature. 321 (6071): 674–679. Bibcode:1986Natur.321..674S. doi:10.1038/321674a0. PMID 3713851. S2CID 27800972. We have developed a method for the partial automation of DNA sequence analysis. Fluorescence detection of the DNA fragments is accomplished by means of a fluorophore covalently attached to the oligonucleotide primer used in enzymatic DNA sequence analysis. A different coloured fluorophore is used for each of the reactions specific for the bases A, C, G and T. The reaction mixtures are combined and co-electrophoresed down a single polyacrylamide gel tube, the separated fluorescent bands of DNA are detected near the bottom of the tube, and the sequence information is acquired directly by computer.
Smith LM, Fung S, Hunkapiller MW, Hunkapiller TJ, Hood LE (April 1985). "The synthesis of oligonucleotides containing an aliphatic amino group at the 5' terminus: synthesis of fluorescent DNA primers for use in DNA sequence analysis". Nucleic Acids Research. 13 (7): 2399–2412. doi:10.1093/nar/13.7.2399. PMC 341163. PMID 4000959.
Crossley, Beate M.; Bai, Jianfa; Glaser, Amy; Maes, Roger; Porter, Elizabeth; Killian, Mary Lea; Clement, Travis; Toohey-Kurth, Kathy (November 2020). "Guidelines for Sanger sequencing and molecular assay monitoring". Journal of Veterinary Diagnostic Investigation. 32 (6): 767–775. doi:10.1177/1040638720905833. ISSN 1040-6387. PMC 7649556. PMID 32070230.
Sanches PR, Charlie-Silva I, Braz HL, Bittar C, Freitas Calmon M, Rahal P, Cilli EM (September 2021). "Recent advances in SARS-CoV-2 Spike protein and RBD mutations comparison between new variants Alpha (B.1.1.7, United Kingdom), Beta (B.1.351, South Africa), Gamma (P.1, Brazil) and Delta (B.1.617.2, India)". Journal of Virus Eradication. 7 (3): 100054. doi:10.1016/j.jve.2021.100054. PMC 8443533. PMID 34548928.
Ledergerber C, Dessimoz C (September 2011). "Base-calling for next-generation sequencing platforms". Briefings in Bioinformatics. 12 (5): 489–497. doi:10.1093/bib/bbq077. PMC 3178052. PMID 21245079.
Murphy KM, Berg KD, Eshleman JR (January 2005). "Sequencing of genomic DNA by combined amplification and cycle sequencing reaction". Clinical Chemistry. 51 (1): 35–39. doi:10.1373/clinchem.2004.039164. PMID 15514094.
SenGupta DJ, Cookson BT (May 2010). "SeqSharp: A general approach for improving cycle-sequencing that facilitates a robust one-step combined amplification and sequencing method". The Journal of Molecular Diagnostics. 12 (3): 272–277. doi:10.2353/jmoldx.2010.090134. PMC 2860461. PMID 20203000.
Kan CW, Fredlake CP, Doherty EA, Barron AE (November 2004). "DNA sequencing and genotyping in miniaturized electrophoresis systems". Electrophoresis. 25 (21–22): 3564–3588. doi:10.1002/elps.200406161. PMID 15565709. S2CID 4851728.
Morozova O, Marra MA (November 2008). "Applications of next-generation sequencing technologies in functional genomics". Genomics. 92 (5): 255–264. doi:10.1016/j.ygeno.2008.07.001. PMID 18703132.
Sinville R, Soper SA (July 2007). "High resolution DNA separations using microchip electrophoresis". Journal of Separation Science. 30 (11): 1714–1728. doi:10.1002/jssc.200700150. PMID 17623451.
Kumar KR, Cowley MJ, Davis RL (October 2019). "Next-Generation Sequencing and Emerging Technologies". Seminars in Thrombosis and Hemostasis. 45 (7): 661–673. doi:10.1055/s-0039-1688446. PMID 31096307.
Mastrorosa FK, Miller DE, Eichler EE (June 2023). "Applications of long-read sequencing to Mendelian genetics". Genome Medicine. 15 (1): 42. doi:10.1186/s13073-023-01194-3. PMC 10266321. PMID 37316925.
Tyson JR, O'Neil NJ, Jain M, Olsen HE, Hieter P, Snutch TP (February 2018). "MinION-based long-read sequencing and assembly extends the Caenorhabditis elegans reference genome". Genome Research. 28 (2): 266–274. doi:10.1101/gr.221184.117. PMC 5793790. PMID 29273626.

ncbi.nlm.nih.gov

Zhang, J (1999-12-15). "A multiple-capillary electrophoresis system for small-scale DNA sequencing and analysis". Nucleic Acids Research. 27 (24): 36e–36. doi:10.1093/nar/27.24.e36. PMC 148759. PMID 10572188.
Daniels RS, Harvey R, Ermetal B, Xiang Z, Galiano M, Adams L, McCauley JW (November 2021). "A Sanger sequencing protocol for SARS-CoV-2 S-gene". Influenza and Other Respiratory Viruses. 15 (6): 707–710. doi:10.1111/irv.12892. PMC 8447197. PMID 34346163.
Vega E, Barclay L, Gregoricus N, Williams K, Lee D, Vinjé J (August 2011). "Novel surveillance network for norovirus gastroenteritis outbreaks, United States". Emerging Infectious Diseases. 17 (8): 1389–1395. doi:10.3201/eid1708.101837. PMC 3381557. PMID 21801614.
Sanger F, Nicklen S, Coulson AR (December 1977). "DNA sequencing with chain-terminating inhibitors". Proceedings of the National Academy of Sciences of the United States of America. 74 (12): 5463–5467. Bibcode:1977PNAS...74.5463S. doi:10.1073/pnas.74.12.5463. PMC 431765. PMID 271968.
Smith LM, Fung S, Hunkapiller MW, Hunkapiller TJ, Hood LE (April 1985). "The synthesis of oligonucleotides containing an aliphatic amino group at the 5' terminus: synthesis of fluorescent DNA primers for use in DNA sequence analysis". Nucleic Acids Research. 13 (7): 2399–2412. doi:10.1093/nar/13.7.2399. PMC 341163. PMID 4000959.
Crossley, Beate M.; Bai, Jianfa; Glaser, Amy; Maes, Roger; Porter, Elizabeth; Killian, Mary Lea; Clement, Travis; Toohey-Kurth, Kathy (November 2020). "Guidelines for Sanger sequencing and molecular assay monitoring". Journal of Veterinary Diagnostic Investigation. 32 (6): 767–775. doi:10.1177/1040638720905833. ISSN 1040-6387. PMC 7649556. PMID 32070230.
Sanches PR, Charlie-Silva I, Braz HL, Bittar C, Freitas Calmon M, Rahal P, Cilli EM (September 2021). "Recent advances in SARS-CoV-2 Spike protein and RBD mutations comparison between new variants Alpha (B.1.1.7, United Kingdom), Beta (B.1.351, South Africa), Gamma (P.1, Brazil) and Delta (B.1.617.2, India)". Journal of Virus Eradication. 7 (3): 100054. doi:10.1016/j.jve.2021.100054. PMC 8443533. PMID 34548928.
Ledergerber C, Dessimoz C (September 2011). "Base-calling for next-generation sequencing platforms". Briefings in Bioinformatics. 12 (5): 489–497. doi:10.1093/bib/bbq077. PMC 3178052. PMID 21245079.
SenGupta DJ, Cookson BT (May 2010). "SeqSharp: A general approach for improving cycle-sequencing that facilitates a robust one-step combined amplification and sequencing method". The Journal of Molecular Diagnostics. 12 (3): 272–277. doi:10.2353/jmoldx.2010.090134. PMC 2860461. PMID 20203000.
Mastrorosa FK, Miller DE, Eichler EE (June 2023). "Applications of long-read sequencing to Mendelian genetics". Genome Medicine. 15 (1): 42. doi:10.1186/s13073-023-01194-3. PMC 10266321. PMID 37316925.
Tyson JR, O'Neil NJ, Jain M, Olsen HE, Hieter P, Snutch TP (February 2018). "MinION-based long-read sequencing and assembly extends the Caenorhabditis elegans reference genome". Genome Research. 28 (2): 266–274. doi:10.1101/gr.221184.117. PMC 5793790. PMID 29273626.

nytimes.com

Taylor DB (2021-03-17). "A Timeline of the Coronavirus Pandemic". The New York Times. ISSN 0362-4331. Retrieved 2021-12-05.

phrap.com

"Phred – Quality Base Calling". Retrieved 2011-02-24.

semanticscholar.org

api.semanticscholar.org

Shendure J, Ji H (October 2008). "Next-generation DNA sequencing". Nature Biotechnology. 26 (10): 1135–1145. doi:10.1038/nbt1486. PMID 18846087. S2CID 6384349.
Smith LM, Sanders JZ, Kaiser RJ, Hughes P, Dodd C, Connell CR, et al. (1986). "Fluorescence detection in automated DNA sequence analysis". Nature. 321 (6071): 674–679. Bibcode:1986Natur.321..674S. doi:10.1038/321674a0. PMID 3713851. S2CID 27800972. We have developed a method for the partial automation of DNA sequence analysis. Fluorescence detection of the DNA fragments is accomplished by means of a fluorophore covalently attached to the oligonucleotide primer used in enzymatic DNA sequence analysis. A different coloured fluorophore is used for each of the reactions specific for the bases A, C, G and T. The reaction mixtures are combined and co-electrophoresed down a single polyacrylamide gel tube, the separated fluorescent bands of DNA are detected near the bottom of the tube, and the sequence information is acquired directly by computer.
Kan CW, Fredlake CP, Doherty EA, Barron AE (November 2004). "DNA sequencing and genotyping in miniaturized electrophoresis systems". Electrophoresis. 25 (21–22): 3564–3588. doi:10.1002/elps.200406161. PMID 15565709. S2CID 4851728.

worldcat.org

search.worldcat.org

Chait, Edward; Page, Guy; Hunkapiller, Michael (1988). "Battle of the DNA sequencers". Nature. 333 (6172): 477–478. Bibcode:1988Natur.333..477C. doi:10.1038/333477a0. ISSN 0028-0836.
Crossley, Beate M.; Bai, Jianfa; Glaser, Amy; Maes, Roger; Porter, Elizabeth; Killian, Mary Lea; Clement, Travis; Toohey-Kurth, Kathy (November 2020). "Guidelines for Sanger sequencing and molecular assay monitoring". Journal of Veterinary Diagnostic Investigation. 32 (6): 767–775. doi:10.1177/1040638720905833. ISSN 1040-6387. PMC 7649556. PMID 32070230.
Taylor DB (2021-03-17). "A Timeline of the Coronavirus Pandemic". The New York Times. ISSN 0362-4331. Retrieved 2021-12-05.