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21“…The precision and robustness of Sanger sequencing contribute significantly to the scientific basis of clinical investigations. …”
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23por Lyons, Elizabeth A, Scheible, Melissa K, Sturk-Andreaggi, Kimberly, Irwin, Jodi A, Just, Rebecca S“…RESULTS: We developed a robust 8-amplicon Sanger sequencing strategy that regularly produces complete, forensic-quality mtGenome haplotypes in the first pass of data generation. …”
Publicado 2013
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24por Cabral, Gabriela Bastos, Ferreira, João Leandro de Paula, de Souza, Renato Pereira, Cunha, Mariana Sequetin, Luchs, Adriana, Figueiredo, Cristina Adelaide, Brígido, Luís Fernando de Macedo“…The identity of Sanger generated sequences with published consensus NGS support the use of Sanger method for ZIKV population studies. …”
Publicado 2017
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25“…Despite its long history, there is a lack of user-friendly Sanger sequencing data analysis tools that can be run interactively as a web application or at large-scale in batch from the command-line. …”
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26“…sangeranalyseR is feature-rich, free, and open-source R package for processing Sanger sequencing data. It allows users to go from loading reads to saving aligned contigs in a few lines of R code by using sensible defaults for most actions. …”
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27por Holt, James M., Kelly, Melissa, Sundlof, Brett, Nakouzi, Ghunwa, Bick, David, Lyon, Elaine“…Employing the algorithm in clinical practice reduced overall orthogonal testing using dideoxynucleotide (Sanger) sequencing by 71%. CONCLUSION: Our results indicate that a low false positive call rate can be maintained while significantly reducing the need for confirmatory testing. …”
Publicado 2021
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28por Daniels, Rodney S., Harvey, Ruth, Ermetal, Burcu, Xiang, Zheng, Galiano, Monica, Adams, Lorin, McCauley, John W.“…We describe a Sanger sequencing protocol for SARS‐CoV‐2 S‐gene the Spike (S)‐glycoprotein product of which, composed of receptor‐binding (S1) and membrane fusion (S2) segments, is the target of vaccines used to combat COVID‐19. …”
Publicado 2021
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29por Furutani, Shunsuke, Furutani, Nozomi, Kawai, Yasuyuki, Nakayama, Akifumi, Nagai, Hidenori“…Thus, the three elemental Sanger-based DNA sequencing steps were accomplished within 41 min. …”
Publicado 2022
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30por Rounds, William H., Ligocki, Ann J., Levin, Mikhail K., Greenberg, Benjamin M., Bigwood, Douglas W., Eastman, Eric M., Cowell, Lindsay G., Monson, Nancy L.“…This antibody gene signature (AGS) was developed using Sanger sequencing of single B cells. While potentially helpful to patients, Sanger sequencing is not an assay that can be practically deployed in clinical settings. …”
Publicado 2014
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31por Jeong, Ji Hun, Lee, Hwan Tae, Seo, Ja Young, Seo, Yiel Hea, Kim, Kyung Hee, Kim, Moon Jin, Lee, Jae Hoon, Park, Jinny, Hong, Jun Shik, Park, Pil Whan, Ahn, Jeong Yeal“…The results were confirmed by Sanger sequencing and compared with results from fragment analysis. …”
Publicado 2016
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33“…According to HTS data, Sanger technology consistently yielded the most abundant photobiont sequence in the sample. …”
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34por Kluesner, Mitchell G., Nedveck, Derek A., Lahr, Walker S., Garbe, John R., Abrahante, Juan E., Webber, Beau R., Moriarity, Branden S.“…To overcome these limitations, we developed a simple, cost-effective, and accurate program to measure base editing efficiency from fluorescence-based Sanger sequencing, termed “EditR.” We provide EditR as a free online tool or downloadable desktop application requiring a single Sanger sequencing file and guide RNA sequence. …”
Publicado 2018
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35High diagnostic yield of direct Sanger sequencing in the diagnosis of neuronal ceroid lipofuscinosespor Jilani, Abdulhakim, Matviychuk, Diana, Blaser, Susan, Dyack, Sarah, Mathieu, Jean, Prasad, Asuri N., Prasad, Chitra, Kyriakopoulou, Lianna, Mercimek‐Andrews, Saadet“…The diagnostic yield of direct Sanger sequencing of CLN genes was 27% in symptomatic patients. …”
Publicado 2019
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36por Rocca, Maria Santa, Ferrarini, Margherita, Msaki, Aichi, Vinanzi, Cinzia, Ghezzi, Marco, De Rocco Ponce, Maurizio, Foresta, Carlo, Ferlin, Alberto“…The accuracy was compared with the results obtained with Sanger. RESULTS: We found that HipSTR was more accurate than Sanger in genotyping normal karyotype men (46,XY), however, it was more likely to misidentify homozygote genotypes in men with Klinefelter syndrome (47,XXY). …”
Publicado 2020
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37por De Cario, Rosina, Kura, Ada, Suraci, Samuele, Magi, Alberto, Volta, Andrea, Marcucci, Rossella, Gori, Anna Maria, Pepe, Guglielmina, Giusti, Betti, Sticchi, Elena“…Variants called following guidelines suggested by the Broad Institute and identified according to MAF <0.01 and allele balance >0.2 were Sanger validated. Three out of 945 validated variants showed a discrepancy between NGS and Sanger. …”
Publicado 2020
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38por Salles, Tiago Souza, Cavalcanti, Andrea Cony, da Costa, Fábio Burack, Dias, Vanessa Zaquieu, de Souza, Leandro Magalhães, de Meneses, Marcelo Damião Ferreira, da Silva, José Antônio Suzano, Amaral, Cinthya Domingues, Felix, Jhonatan Ramos, Pereira, Duleide Alves, Boatto, Stefanella, Guimarães, Maria Angélica Arpon Marandino, Ferreira, Davis Fernandes, Azevedo, Renata Campos“…Therefore, to support the urgent surveillance of SARS-CoV-2 S gene, this work describes a new feasible protocol for complete nucleotide sequencing of the S gene using the Sanger technique. Such a methodology could be easily adopted by any laboratory with experience in sequencing, adding to effective surveillance of SARS-CoV-2 spreading and evolution.…”
Publicado 2022
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39por Ayoup, Mohammed Salah, Rabee, Ahmed R., Abdel-Hamid, Hamida, Harras, Marwa F., El Menofy, Nagwan G., Ismail, Magda M. F.“…[Image: see text] Facile synthesis of molecular hybrids containing a 2,4-dinitrophenyl moiety was achieved via nucleophilic aromatic substitution of the fluoride anion of Sanger’s reagent (2,4-dinitrofluorobenzene) with various N, S, and O nucleophiles, considered as bioactive moieties. …”
Publicado 2022
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40por Li, Jinhui, Yang, Lang, Wang, Kaiying, Gao, Zhiyong, Li, Peihan, Lin, Yanfeng, Jia, Leili, Wang, Quanyi, Song, Hongbin, Li, Peng“…Samples were evaluated immediately using parallel multiplex RT-qPCR and nanopore sequencing, and were then amplified by designed primers and Sanger sequencing to obtain whole genome sequences. …”
Publicado 2023
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