Literature DB >> 33542447

Adaptor Template Oligo-Mediated Sequencing (ATOM-Seq) is a new ultra-sensitive UMI-based NGS library preparation technology for use with cfDNA and cfRNA.

Thomas L Dunwell1, Simon C Dailey1, Anine L Ottestad2,3, Jihang Yu1, Philipp W Becker1, Sarah Scaife1, Susan D Richman4, Henry M Wood4, Hayley Slaney4, Daniel Bottomley4, Xiangsheng Yang5, Hui Xiao5, Sissel G F Wahl2,3, Bjørn H Grønberg2,3, Hongyan Dai2,6, Guoliang Fu7.   

Abstract

Liquid biopsy testing utilising Next Generation Sequencing (NGS) is rapidly moving towards clinical adoption for personalised oncology. However, before NGS can fulfil its potential any novel testing approach must identify ways of reducing errors, allowing separation of true low-frequency mutations from procedural artefacts, and be designed to improve upon current technologies. Popular NGS technologies typically utilise two DNA capture approaches; PCR and ligation, which have known limitations and seem to have reached a development plateau with only small, stepwise improvements being made. To maximise the ultimate utility of liquid biopsy testing we have developed a highly versatile approach to NGS: Adaptor Template Oligo Mediated Sequencing (ATOM-Seq). ATOM-Seq's strengths and versatility avoid the major limitations of both PCR- and ligation-based approaches. This technology is ligation free, simple, efficient, flexible, and streamlined, and it offers novel advantages that make it perfectly suited for use on highly challenging clinical material. Using reference and clinical materials, we demonstrate detection of known SNVs down to allele frequencies of 0.1% using as little as 20-25 ng of cfDNA, as well as the ability to detect fusions from RNA. We illustrate ATOM-Seq's suitability for clinical testing by showing high concordance rates between paired cfDNA and FFPE clinical samples.

Entities:  

Mesh:

Substances:

Year:  2021        PMID: 33542447      PMCID: PMC7862664          DOI: 10.1038/s41598-021-82737-9

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


  26 in total

1.  Detection and quantification of rare mutations with massively parallel sequencing.

Authors:  Isaac Kinde; Jian Wu; Nick Papadopoulos; Kenneth W Kinzler; Bert Vogelstein
Journal:  Proc Natl Acad Sci U S A       Date:  2011-05-17       Impact factor: 11.205

2.  Comprehensive Characterization of Cancer Driver Genes and Mutations.

Authors:  Matthew H Bailey; Collin Tokheim; Eduard Porta-Pardo; Sohini Sengupta; Denis Bertrand; Amila Weerasinghe; Antonio Colaprico; Michael C Wendl; Jaegil Kim; Brendan Reardon; Patrick Kwok-Shing Ng; Kang Jin Jeong; Song Cao; Zixing Wang; Jianjiong Gao; Qingsong Gao; Fang Wang; Eric Minwei Liu; Loris Mularoni; Carlota Rubio-Perez; Niranjan Nagarajan; Isidro Cortés-Ciriano; Daniel Cui Zhou; Wen-Wei Liang; Julian M Hess; Venkata D Yellapantula; David Tamborero; Abel Gonzalez-Perez; Chayaporn Suphavilai; Jia Yu Ko; Ekta Khurana; Peter J Park; Eliezer M Van Allen; Han Liang; Michael S Lawrence; Adam Godzik; Nuria Lopez-Bigas; Josh Stuart; David Wheeler; Gad Getz; Ken Chen; Alexander J Lazar; Gordon B Mills; Rachel Karchin; Li Ding
Journal:  Cell       Date:  2018-04-05       Impact factor: 41.582

3.  A method for counting PCR template molecules with application to next-generation sequencing.

Authors:  James A Casbon; Robert J Osborne; Sydney Brenner; Conrad P Lichtenstein
Journal:  Nucleic Acids Res       Date:  2011-04-13       Impact factor: 16.971

4.  Detecting very low allele fraction variants using targeted DNA sequencing and a novel molecular barcode-aware variant caller.

Authors:  Chang Xu; Mohammad R Nezami Ranjbar; Zhong Wu; John DiCarlo; Yexun Wang
Journal:  BMC Genomics       Date:  2017-01-03       Impact factor: 3.969

5.  Characterization of background noise in capture-based targeted sequencing data.

Authors:  Gahee Park; Joo Kyung Park; Seung-Ho Shin; Hyo-Jeong Jeon; Nayoung K D Kim; Yeon Jeong Kim; Hyun-Tae Shin; Eunjin Lee; Kwang Hyuck Lee; Dae-Soon Son; Woong-Yang Park; Donghyun Park
Journal:  Genome Biol       Date:  2017-07-21       Impact factor: 13.583

6.  SPlinted Ligation Adapter Tagging (SPLAT), a novel library preparation method for whole genome bisulphite sequencing.

Authors:  Amanda Raine; Erika Manlig; Per Wahlberg; Ann-Christine Syvänen; Jessica Nordlund
Journal:  Nucleic Acids Res       Date:  2017-04-07       Impact factor: 16.971

7.  SALP, a new single-stranded DNA library preparation method especially useful for the high-throughput characterization of chromatin openness states.

Authors:  Jian Wu; Wei Dai; Lin Wu; Jinke Wang
Journal:  BMC Genomics       Date:  2018-02-13       Impact factor: 3.969

8.  fastp: an ultra-fast all-in-one FASTQ preprocessor.

Authors:  Shifu Chen; Yanqing Zhou; Yaru Chen; Jia Gu
Journal:  Bioinformatics       Date:  2018-09-01       Impact factor: 6.937

9.  Fragment Length of Circulating Tumor DNA.

Authors:  Hunter R Underhill; Jacob O Kitzman; Sabine Hellwig; Noah C Welker; Riza Daza; Daniel N Baker; Keith M Gligorich; Robert C Rostomily; Mary P Bronner; Jay Shendure
Journal:  PLoS Genet       Date:  2016-07-18       Impact factor: 5.917

10.  Validation of the Oncomine focus panel for next-generation sequencing of clinical tumour samples.

Authors:  Hannah L Williams; Kathy Walsh; Austin Diamond; Anca Oniscu; Zandra C Deans
Journal:  Virchows Arch       Date:  2018-08-13       Impact factor: 4.064

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.