Literature DB >> 26423591

Overview of Target Enrichment Strategies.

Iwanka Kozarewa1, Javier Armisen2, Andrew F Gardner3, Barton E Slatko3, C L Hendrickson4.   

Abstract

Target enrichment is commonly used in next generation sequencing (NGS) workflows to eliminate genomic DNA regions that are not of interest for a particular experiment. By only targeting specific regions such as exons, one can obtain greater depth of DNA sequencing coverage for regions of interest or increase the sampling numbers of individuals, thereby saving both time and cost. This overview of target enrichment strategies provides a high-level review of distinct approaches to capture specific sequences: (a) hybridization-based strategies, (b) transposon-mediated fragmentation (tagmentation), (c) molecular inversion probes (MIPs), and (d) singleplex and multiplex polymerase chain reaction (PCR) target enrichment. Strategies for assay design and performance criteria are also discussed. Other platforms currently in development are also briefly described.
Copyright © 2015 John Wiley & Sons, Inc.

Keywords:  DNA capture; PCR amplification; hybridization based enrichment; target enrichment

Mesh:

Year:  2015        PMID: 26423591     DOI: 10.1002/0471142727.mb0721s112

Source DB:  PubMed          Journal:  Curr Protoc Mol Biol        ISSN: 1934-3647


  20 in total

1.  Assembly of Long-Adapter Single-Strand Oligonucleotide (LASSO) Probes for Massively Parallel Capture of Kilobase Size DNA Targets.

Authors:  Lamia Chkaiban; Lorenzo Tosi; Biju Parekkadan
Journal:  Curr Protoc       Date:  2021-11

2.  Targeted Virome Sequencing Enhances Unbiased Detection and Genome Assembly of Known and Emerging Viruses-The Example of SARS-CoV-2.

Authors:  Vasiliki Pogka; Gethsimani Papadopoulou; Vaia Valiakou; Dionyssios N Sgouras; Andreas F Mentis; Timokratis Karamitros
Journal:  Viruses       Date:  2022-06-11       Impact factor: 5.818

Review 3.  Cell free DNA as a diagnostic and prognostic marker for cardiovascular diseases.

Authors:  Iuliia A Polina; Daria V Ilatovskaya; Kristine Y DeLeon-Pennell
Journal:  Clin Chim Acta       Date:  2020-01-21       Impact factor: 3.786

4.  Performance and automation of ancient DNA capture with RNA hyRAD probes.

Authors:  Tomasz Suchan; Mariya A Kusliy; Naveed Khan; Loreleï Chauvey; Laure Tonasso-Calvière; Stéphanie Schiavinato; John Southon; Marcel Keller; Keiko Kitagawa; Johannes Krause; Alexander N Bessudnov; Alexander A Bessudnov; Alexander S Graphodatsky; Silvia Valenzuela-Lamas; Jarosław Wilczyński; Sylwia Pospuła; Krzysztof Tunia; Marek Nowak; Magdalena Moskal-delHoyo; Alexey A Tishkin; Alexander J E Pryor; Alan K Outram; Ludovic Orlando
Journal:  Mol Ecol Resour       Date:  2021-10-15       Impact factor: 8.678

5.  Development and evaluation of ActSeq: A targeted next-generation sequencing panel for clinical oncology use.

Authors:  Zonggao Shi; Jacqueline Lopez; William Kalliney; Bobbie Sutton; Joyce Simpson; Kevin Maggert; Sheng Liu; Jun Wan; M Sharon Stack
Journal:  PLoS One       Date:  2022-04-21       Impact factor: 3.240

6.  Targeted Next-Generation Sequencing of 117 Routine Clinical Samples Provides Further Insights into the Molecular Landscape of Uveal Melanoma.

Authors:  Sophie Thornton; Sarah E Coupland; Lisa Olohan; Julie S Sibbring; John G Kenny; Christiane Hertz-Fowler; Xuan Liu; Sam Haldenby; Heinrich Heimann; Rumana Hussain; Natalie Kipling; Azzam Taktak; Helen Kalirai
Journal:  Cancers (Basel)       Date:  2020-04-23       Impact factor: 6.639

7.  Targeted genome fragmentation with CRISPR/Cas9 enables fast and efficient enrichment of small genomic regions and ultra-accurate sequencing with low DNA input (CRISPR-DS).

Authors:  Scott R Kennedy; Rosa Ana Risques; Daniela Nachmanson; Shenyi Lian; Elizabeth K Schmidt; Michael J Hipp; Kathryn T Baker; Yuezheng Zhang; Maria Tretiakova; Kaitlyn Loubet-Senear; Brendan F Kohrn; Jesse J Salk
Journal:  Genome Res       Date:  2018-09-19       Impact factor: 9.043

8.  Hybrid Capture-Based Next Generation Sequencing and Its Application to Human Infectious Diseases.

Authors:  Maxime Gaudin; Christelle Desnues
Journal:  Front Microbiol       Date:  2018-11-27       Impact factor: 5.640

9.  A comprehensive assessment of Next-Generation Sequencing variants validation using a secondary technology.

Authors:  Jianchao Zheng; Hongyun Zhang; Santasree Banerjee; Yun Li; Junyu Zhou; Qian Yang; Xuemei Tan; Peng Han; Qinmei Fu; Xiaoli Cui; Yuying Yuan; Meiyan Zhang; Ruiqin Shen; Haifeng Song; Xiuqing Zhang; Lijian Zhao; Zhiyu Peng; Wei Wang; Ye Yin
Journal:  Mol Genet Genomic Med       Date:  2019-06-04       Impact factor: 2.183

10.  The reliable assurance of detecting somatic mutations in cancer-related genes by next-generation sequencing: the results of external quality assessment in China.

Authors:  Rui Zhang; Jiansheng Ding; Yanxi Han; Lang Yi; Jiehong Xie; Xin Yang; Gaowei Fan; Guojing Wang; Mingju Hao; Dong Zhang; Kuo Zhang; Guigao Lin; Jinming Li
Journal:  Oncotarget       Date:  2016-09-06
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