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Material Type: Bài báo
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Toward best practice in cancer mutation detection with whole-genome and whole-exome sequencingNature biotechnology, 2021-09, Vol.39 (9), p.1141-1150 [Tạp chí có phản biện]2021. This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply. ;COPYRIGHT 2021 Nature Publishing Group ;This is a U.S. government work and not under copyright protection in the U.S.; foreign copyright protection may apply 2021. ;ISSN: 1087-0156 ;ISSN: 1546-1696 ;EISSN: 1546-1696 ;DOI: 10.1038/s41587-021-00994-5 ;PMID: 34504346Tài liệu số/Tài liệu điện tử |
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Material Type: Bài báo
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Sequencing-based methods and resources to study antimicrobial resistanceNature reviews. Genetics, 2019-06, Vol.20 (6), p.356-370 [Tạp chí có phản biện]COPYRIGHT 2019 Nature Publishing Group ;2019© Springer Nature Limited 2019 ;ISSN: 1471-0056 ;EISSN: 1471-0064 ;DOI: 10.1038/s41576-019-0108-4 ;PMID: 30886350Tài liệu số/Tài liệu điện tử |
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Material Type: Bài báo
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DengueSeq: a pan-serotype whole genome amplicon sequencing protocol for dengue virusBMC genomics, 2024-05, Vol.25 (1), p.433-433 [Tạp chí có phản biện]2024. The Author(s). ;COPYRIGHT 2024 BioMed Central Ltd. ;2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2024 ;ISSN: 1471-2164 ;EISSN: 1471-2164 ;DOI: 10.1186/s12864-024-10350-x ;PMID: 38693476Tài liệu số/Tài liệu điện tử |
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Material Type: Bài báo
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Trycycler: consensus long-read assemblies for bacterial genomesGenome Biology, 2021-09, Vol.22 (1), p.266-266, Article 266 [Tạp chí có phản biện]2021. The Author(s). ;2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 1474-760X ;ISSN: 1474-7596 ;EISSN: 1474-760X ;DOI: 10.1186/s13059-021-02483-z ;PMID: 34521459Tài liệu số/Tài liệu điện tử |
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Material Type: Bài báo
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Third-Generation Sequencing: The Spearhead towards the Radical Transformation of Modern GenomicsLife (Basel, Switzerland), 2021-12, Vol.12 (1), p.30 [Tạp chí có phản biện]2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;2021 by the authors. 2021 ;ISSN: 2075-1729 ;EISSN: 2075-1729 ;DOI: 10.3390/life12010030 ;PMID: 35054423Tài liệu số/Tài liệu điện tử |
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Material Type: Bài báo
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SMOOTH-seq: single-cell genome sequencing of human cells on a third-generation sequencing platformGenome Biology, 2021-06, Vol.22 (1), p.195-195, Article 195 [Tạp chí có phản biện]2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2021 ;ISSN: 1474-760X ;ISSN: 1474-7596 ;EISSN: 1474-760X ;DOI: 10.1186/s13059-021-02406-y ;PMID: 34193237Tài liệu số/Tài liệu điện tử |
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Material Type: Bài báo
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A Randomized, Controlled Trial of the Analytic and Diagnostic Performance of Singleton and Trio, Rapid Genome and Exome Sequencing in Ill InfantsAmerican journal of human genetics, 2019-10, Vol.105 (4), p.719-733 [Tạp chí có phản biện]2019 American Society of Human Genetics ;Copyright © 2019 American Society of Human Genetics. Published by Elsevier Inc. All rights reserved. ;2019 American Society of Human Genetics. 2019 American Society of Human Genetics ;ISSN: 0002-9297 ;EISSN: 1537-6605 ;DOI: 10.1016/j.ajhg.2019.08.009 ;PMID: 31564432Tài liệu số/Tài liệu điện tử |
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Material Type: Bài báo
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The complete costs of genome sequencing: a microcosting study in cancer and rare diseases from a single center in the United KingdomGenetics in medicine, 2020-01, Vol.22 (1), p.85-94 [Tạp chí có phản biện]2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. ;The Author(s) 2019 ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/s41436-019-0618-7 ;PMID: 31358947Tài liệu số/Tài liệu điện tử |
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9 |
Material Type: Bài báo
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Characterization and remediation of sample index swaps by non-redundant dual indexing on massively parallel sequencing platformsBMC genomics, 2018-05, Vol.19 (1), p.332-332, Article 332 [Tạp chí có phản biện]COPYRIGHT 2018 BioMed Central Ltd. ;COPYRIGHT 2018 BioMed Central Ltd. ;The Author(s). 2018 ;ISSN: 1471-2164 ;EISSN: 1471-2164 ;DOI: 10.1186/s12864-018-4703-0 ;PMID: 29739332Tài liệu số/Tài liệu điện tử |
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10 |
Material Type: Bài báo
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Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic testGenetics in medicine, 2018-04, Vol.20 (4), p.435-443 [Tạp chí có phản biện]Copyright Nature Publishing Group Apr 2018 ;Copyright © 2018 The Author(s) 2018 The Author(s) ;ISSN: 1098-3600 ;EISSN: 1530-0366 ;DOI: 10.1038/gim.2017.119 ;PMID: 28771251Tài liệu số/Tài liệu điện tử |