Literature DB >> 22237533

Generating barcoded libraries for multiplex high-throughput sequencing.

Michael Knapp1, Mathias Stiller, Matthias Meyer.   

Abstract

Molecular barcoding is an essential tool to use the high throughput of next generation sequencing platforms optimally in studies involving more than one sample. Various barcoding strategies allow for the incorporation of short recognition sequences (barcodes) into sequencing libraries, either by ligation or polymerase chain reaction (PCR). Here, we present two approaches optimized for generating barcoded sequencing libraries from low copy number extracts and amplification products typical of ancient DNA studies.

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Year:  2012        PMID: 22237533     DOI: 10.1007/978-1-61779-516-9_19

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


  11 in total

1.  Aboriginal mitogenomes reveal 50,000 years of regionalism in Australia.

Authors:  Ray Tobler; Adam Rohrlach; Julien Soubrier; Pere Bover; Bastien Llamas; Jonathan Tuke; Nigel Bean; Ali Abdullah-Highfold; Shane Agius; Amy O'Donoghue; Isabel O'Loughlin; Peter Sutton; Fran Zilio; Keryn Walshe; Alan N Williams; Chris S M Turney; Matthew Williams; Stephen M Richards; Robert J Mitchell; Emma Kowal; John R Stephen; Lesley Williams; Wolfgang Haak; Alan Cooper
Journal:  Nature       Date:  2017-03-08       Impact factor: 49.962

2.  Complete mitochondrial DNA genome sequences from the first New Zealanders.

Authors:  Michael Knapp; K Ann Horsburgh; Stefan Prost; Jo-Ann Stanton; Hallie R Buckley; Richard K Walter; Elizabeth A Matisoo-Smith
Journal:  Proc Natl Acad Sci U S A       Date:  2012-10-22       Impact factor: 11.205

3.  Advanced paternal age does not affect embryo aneuploidy following blastocyst biopsy in egg donor cycles.

Authors:  Robert J Carrasquillo; Taylor P Kohn; Cengiz Cinnioglu; Carmen Rubio; Carlos Simon; Ranjith Ramasamy; Nasser Al-Asmar
Journal:  J Assist Reprod Genet       Date:  2019-08-05       Impact factor: 3.412

4.  Application of next-generation sequencing for 24-chromosome aneuploidy screening of human preimplantation embryos.

Authors:  Haiyan Zheng; Hua Jin; Lian Liu; Jianqiao Liu; Wei-Hua Wang
Journal:  Mol Cytogenet       Date:  2015-06-16       Impact factor: 2.009

5.  Multiplexed Illumina sequencing libraries from picogram quantities of DNA.

Authors:  Sarah K Bowman; Matthew D Simon; Aimee M Deaton; Michael Tolstorukov; Mark L Borowsky; Robert E Kingston
Journal:  BMC Genomics       Date:  2013-07-09       Impact factor: 3.969

6.  High-throughput ultrastructure screening using electron microscopy and fluorescent barcoding.

Authors:  Yury S Bykov; Nir Cohen; Natalia Gabrielli; Hetty Manenschijn; Sonja Welsch; Petr Chlanda; Wanda Kukulski; Kiran R Patil; Maya Schuldiner; John A G Briggs
Journal:  J Cell Biol       Date:  2019-07-09       Impact factor: 10.539

7.  Low-cost cross-taxon enrichment of mitochondrial DNA using in-house synthesised RNA probes.

Authors:  Stephen M Richards; Nelli Hovhannisyan; Matthew Gilliham; Joshua Ingram; Birgitte Skadhauge; Holly Heiniger; Bastien Llamas; Kieren J Mitchell; Julie Meachen; Geoffrey B Fincher; Jeremy J Austin; Alan Cooper
Journal:  PLoS One       Date:  2019-02-04       Impact factor: 3.240

8.  Complete Mitochondrial Genomes of New Zealand's First Dogs.

Authors:  Karen Greig; James Boocock; Stefan Prost; K Ann Horsburgh; Chris Jacomb; Richard Walter; Elizabeth Matisoo-Smith
Journal:  PLoS One       Date:  2015-10-07       Impact factor: 3.240

9.  DNA capture and next-generation sequencing can recover whole mitochondrial genomes from highly degraded samples for human identification.

Authors:  Jennifer E L Templeton; Paul M Brotherton; Bastien Llamas; Julien Soubrier; Wolfgang Haak; Alan Cooper; Jeremy J Austin
Journal:  Investig Genet       Date:  2013-12-02

Review 10.  Validation of high throughput sequencing and microbial forensics applications.

Authors:  Bruce Budowle; Nancy D Connell; Anna Bielecka-Oder; Rita R Colwell; Cindi R Corbett; Jacqueline Fletcher; Mats Forsman; Dana R Kadavy; Alemka Markotic; Stephen A Morse; Randall S Murch; Antti Sajantila; Sarah E Schmedes; Krista L Ternus; Stephen D Turner; Samuel Minot
Journal:  Investig Genet       Date:  2014-07-30
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