Literature DB >> 27822865

Targeted Locus Amplification and Next-Generation Sequencing.

Quint P Hottentot1, M van Min2, E Splinter3, Stefan J White4.   

Abstract

Despite developments in targeted and whole-genome sequencing, the robust detection of all genetic variation, including structural variants, in and around genes of interest and in an allele-specific manner remains a challenge. Targeted locus amplification (TLA) is a cross-linking-based technique that generates complex DNA libraries covering >100 kb of contiguous sequence surrounding one primer pair complementary to a short locus-specific sequence. In combination with next-generation sequencing, TLA enables the complete sequencing and haplotyping of targeted regions of interest. Here we outline the basis of TLA, together with a detailed protocol of the technique.

Keywords:  Copy number variation; Next-generation sequencing; Structural variation; Variant detection

Mesh:

Substances:

Year:  2017        PMID: 27822865     DOI: 10.1007/978-1-4939-6442-0_13

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  12 in total

1.  Minimal residual disease in mantle cell lymphoma: are we ready for a personalized treatment approach?

Authors:  Simone Ferrero; Martin Dreyling
Journal:  Haematologica       Date:  2017-07       Impact factor: 9.941

2.  Mapping Transgene Insertion Sites Reveals Complex Interactions Between Mouse Transgenes and Neighboring Endogenous Genes.

Authors:  Mallory A Laboulaye; Xin Duan; Mu Qiao; Irene E Whitney; Joshua R Sanes
Journal:  Front Mol Neurosci       Date:  2018-10-23       Impact factor: 5.639

3.  Remapping of the belted phenotype in cattle on BTA3 identifies a multiplication event as the candidate causal mutation.

Authors:  Sophie Rothammer; Elisabeth Kunz; Stefan Krebs; Fanny Bitzer; Andreas Hauser; Natalia Zinovieva; Nikolai Klymiuk; Ivica Medugorac
Journal:  Genet Sel Evol       Date:  2018-07-06       Impact factor: 4.297

4.  Large-scale discovery of mouse transgenic integration sites reveals frequent structural variation and insertional mutagenesis.

Authors:  Leslie O Goodwin; Erik Splinter; Tiffany L Davis; Rachel Urban; Hao He; Robert E Braun; Elissa J Chesler; Vivek Kumar; Max van Min; Juliet Ndukum; Vivek M Philip; Laura G Reinholdt; Karen Svenson; Jacqueline K White; Michael Sasner; Cathleen Lutz; Stephen A Murray
Journal:  Genome Res       Date:  2019-01-18       Impact factor: 9.043

5.  Variation in zygotic CRISPR/Cas9 gene editing outcomes generates novel reporter and deletion alleles at the Gdf11 locus.

Authors:  Jill M Goldstein; Austin Valido; Jordan P Lewandowski; Ryan G Walker; Melanie J Mills; Kathleen A Messemer; Paul Besseling; Kyu Ha Lee; Samuel J Wattrus; Miook Cho; Richard T Lee; Amy J Wagers
Journal:  Sci Rep       Date:  2019-12-09       Impact factor: 4.379

6.  Minimal residual disease (MRD) detection in acute lymphoblastic leukaemia based on fusion genes and genomic deletions: towards MRD for all.

Authors:  Roland P Kuiper; Patricia G Hoogeveen; Reno Bladergroen; Freerk van Dijk; Edwin Sonneveld; Frank N van Leeuwen; Judith Boer; Irina Sergeeva; Harma Feitsma; Monique L den Boer; Vincent H J van der Velden
Journal:  Br J Haematol       Date:  2021-08-01       Impact factor: 8.615

7.  Editing out five Serpina1 paralogs to create a mouse model of genetic emphysema.

Authors:  Florie Borel; Huaming Sun; Marina Zieger; Andrew Cox; Brynn Cardozo; Weiying Li; Gabriella Oliveira; Airiel Davis; Alisha Gruntman; Terence R Flotte; Michael H Brodsky; Andrew M Hoffman; Mai K Elmallah; Christian Mueller
Journal:  Proc Natl Acad Sci U S A       Date:  2018-02-16       Impact factor: 11.205

Review 8.  Three-dimensional genome architecture and emerging technologies: looping in disease.

Authors:  Arpit Mishra; R David Hawkins
Journal:  Genome Med       Date:  2017-09-30       Impact factor: 11.117

9.  A Novel t(8;14)(q24;q11) Rearranged Human Cell Line as a Model for Mechanistic and Drug Discovery Studies of NOTCH1-Independent Human T-Cell Leukemia.

Authors:  Valeria Tosello; Gloria Milani; Annalisa Martines; Nadia Macri; Wouder Van Loocke; Filip Matthijssens; Barbara Buldini; Sonia Minuzzo; Deborah Bongiovanni; Richard Fabian Schumacher; Alberto Amadori; Pieter Van Vlierberghe; Erich Piovan
Journal:  Cells       Date:  2018-10-09       Impact factor: 6.600

10.  Induction of a chromatin boundary in vivo upon insertion of a TAD border.

Authors:  Andréa Willemin; Lucille Lopez-Delisle; Christopher Chase Bolt; Marie-Laure Gadolini; Denis Duboule; Eddie Rodriguez-Carballo
Journal:  PLoS Genet       Date:  2021-07-22       Impact factor: 5.917

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