Zobrazeno 1 - 10
of 1 273
pro vyhledávání: '"Semiconductor sequencing"'
Autor:
Li-Ya Wang, Xing-Qiang Rao, Yu-Qin Luo, Bei Liu, Chun-Fang Peng, Dan Chen, Kai Yan, Ye-Qing Qian, Yan-Mei Yang, Ying-Zhi Huang, Min Chen, Yi-Xi Sun, Hong-Ge Li, Ying-Hui Ye, Fan Jin, Hai-Liang Liu, Min-Yue Dong
Publikováno v:
Human Genomics, Vol 13, Iss 1, Pp 1-8 (2019)
Abstract Background Recent advances in semiconductor sequencing platform (SSP) have provided new methods for preimplantation genetic diagnosis/screening (PGD/S). The present study aimed to evaluate the applicability and efficiency of SSP in PGD/S. Me
Externí odkaz:
https://doaj.org/article/91cb0291047146fea23a439432233bf5
Autor:
Yin, Ai-hua, Peng, Chun-fang, Zhao, Xin, Caughey, Bennett A., Yang, Jie-xia, Liu, Jian, Huang, Wei-wei, Liu, Chang, Luo, Dong-hong, Liu, Hai-liang, Chen, Yang-yi, Wu, Jing, Hou, Rui, Zhang, Mindy, Ai, Michael, Zheng, Lianghong, Xue, Rachel Q., Mai, Ming-qin, Guo, Fang-fang, Qi, Yi-ming, Wang, Dong-mei, Krawczyk, Michal, Zhang, Daniel, Wang, Yu-nan, Huang, Quan-fei, Karin, Michael, Zhang, Kang
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 2015 Nov . 112(47), 14670-14675.
Externí odkaz:
https://www.jstor.org/stable/26465876
Autor:
Tiago César Gouvêa Moreira, Micheline Campos Rezende, Fábio Borges Mury, Luciana de Andrade Agostinho, Carla Simone Moreira de Freitas, Pricila da Silva Spinola, Cibele R. Bonvicino, Cibele Rodrigues Bonvicino
Publikováno v:
Biomédica
Biomédica: revista del Instituto Nacional de Salud, Vol 41, Iss 4, Pp 773-786 (2021)
Biomédica, Volume: 41, Issue: 4, Pages: 773-786, Published: 15 DEC 2021
Biomédica: revista del Instituto Nacional de Salud, Vol 41, Iss 4, Pp 773-786 (2021)
Biomédica, Volume: 41, Issue: 4, Pages: 773-786, Published: 15 DEC 2021
Introduction: Next Generation Sequencing (NGS) is cost-effective and a faster method to study genes, but its protocol is challenging. Objective: To analyze different adjustments to the protocol for screening the BRCA genes using Ion Torrent PGM seque
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a86b22a41d9d5e624cb1c522a740a61d
https://doi.org/10.7705/biomedica.5663
https://doi.org/10.7705/biomedica.5663
Publikováno v:
Human Immunology. 82:812-819
Next-generation sequencing (NGS), also known as massively parallel sequencing, has revolutionized genomic research. The current advances in NGS technology make it possible to provide high resolution, high throughput HLA typing in clinical laboratorie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5712097a267b13c64b40300966036faa
https://doi.org/10.1016/j.humimm.2021.03.011
https://doi.org/10.1016/j.humimm.2021.03.011
Publikováno v:
Analytical Chemistry
Isothermal recombinase polymerase amplification-based solid-phase primer extension is used for the optical detection of a hypertrophic cardiomyopathy associated single nucleotide polymorphism (SNP) in a fingerprick blood sample. The assay exploits fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66f75f4f18d7e10c76337d74b4146b2d
https://doi.org/10.1021/acs.analchem.1c03419
https://doi.org/10.1021/acs.analchem.1c03419
Autor:
Harriet Feilotter, David Good, Annette E. Hay, Nancy Carson, Christina K. Ferrone, Brooke Snetsinger, Michael J. Rauh, Guillaume Richard-Carpentier, Susan Crocker, Grace Zhang, Xiao Zhang, Barnaba Werunga, Graeme Quest, Laura Semenuk, Henry K. Wong, Janet Lui
Publikováno v:
The Journal of Molecular Diagnostics. 23:1292-1305
The identification of clinically significant genes recurrently mutated in myeloid malignancies necessitates expanding diagnostic testing with higher throughput, such as targeted next-generation sequencing. We present validation of the Thermo Fisher O
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::100eabfd0392b5d53b44a71678ddae99
https://doi.org/10.1016/j.jmoldx.2021.07.010
https://doi.org/10.1016/j.jmoldx.2021.07.010
Publikováno v:
The Journal of Molecular Diagnostics. 23:1241-1248
Next-generation sequencing (NGS) has proved to be a beneficial approach for genotyping solid tumor specimens and for identifying clinically actionable mutations. However, copy number variations (CNVs), which can be equally important, are often challe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::785f4483443c1d4c0689a4869f197a81
https://doi.org/10.1016/j.jmoldx.2021.07.016
https://doi.org/10.1016/j.jmoldx.2021.07.016
Autor:
Eszter Mihalov-Kovács, Ákos Gellért, Szilvia Marton, Szilvia L. Farkas, Enikő Fehér, Miklós Oldal, Ferenc Jakab, Vito Martella, Krisztián Bányai
Publikováno v:
Emerging Infectious Diseases, Vol 21, Iss 4, Pp 660-663 (2015)
We identified unusual rotavirus strains in fecal specimens from sheltered dogs in Hungary by viral metagenomics. The novel rotavirus species displayed limited genome sequence homology to representatives of the 8 rotavirus species, A–H, and qualifie
Externí odkaz:
https://doaj.org/article/397dcddd8b1c4610a7783cbba7b29bd7
Autor:
Mei‑Juan Xie, Shou‑Fang Qu, Xue-Xi Yang, Long Wu, Zhi‑Kun Liang, Fen‑Xia Li, Dan He, Fang Yang, Ying‑Song Wu
Publikováno v:
Molecular Medicine Reports
Chromosomal abnormalities (CAs) can cause spontaneous miscarriage and increase the incidence of subsequent pregnancy loss and other complications. Presently, CAs are detected mainly by array comparative genomic hybridization (CGH) and single nucleoti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12ddbdc50fbdcd0f04c6d08c4bd754c8
https://doi.org/10.3892/mmr.2020.11208
https://doi.org/10.3892/mmr.2020.11208
Autor:
Shalini Anandan, Dhirendra Kumar, Lucky Sangal, Dhiviya Prabaa Muthuirulandi Sethuvel, Naresh Chand Sharma, Balaji Veeraraghavan, Naveen Kumar Devanga Ragupathi, Karthick Vasudevan, Sushil K. Gupta
Publikováno v:
Journal of Genomics
Objectives: Pertussis is a highly contagious disease of the respiratory tract caused by Bordetella pertussis, a bacterium that lives in the mouth, nose, and throat. Current study reports the highly accurate complete genomes of two clinical B. pertuss
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf7a09f9df78954b9d4ed4fb6e207d7f
http://europepmc.org/articles/PMC8437686
http://europepmc.org/articles/PMC8437686