Library Construction for High-Throughput Mobile Element Identification and Genotyping

Author(s):  
Hongseok Ha ◽  
Nan Wang ◽  
Jinchuan Xing

2018 ◽  
Author(s):  
Jiyeon Kweon ◽  
Da-eun Kim ◽  
An-Hee Jang ◽  
Yongsub Kim

ABSCTRACTAlthough pooled CRISPR libraries are widely used in high-throughput screening to study various biological processes, library construction for researcher’s own study is a time-consuming, labor-intensive, and expensive process. In this study, we develop a simple, scalable method, called Cas-CLIP, to customize conventional pooled CRISPR libraries using the CRISPR/Cas9 system. We show that conventional pooled CRISPR libraries can be modified by eliminating gRNAs that target positive genes, enabling the identification of unknown target genes in CRISPR screening. Cas-CLIP is a precise method for customizing conventional pooled CRISPR libraries and will broaden the scope of high-throughput screening technology.



BMC Genomics ◽  
2010 ◽  
Vol 11 (1) ◽  
pp. 410 ◽  
Author(s):  
David J Witherspoon ◽  
Jinchuan Xing ◽  
Yuhua Zhang ◽  
W Scott Watkins ◽  
Mark A Batzer ◽  
...  


2013 ◽  
Vol 29 (5) ◽  
pp. 280-289 ◽  
Author(s):  
Jinchuan Xing ◽  
David J. Witherspoon ◽  
Lynn B. Jorde


2007 ◽  
Vol 3 (1) ◽  
pp. 48-57 ◽  
Author(s):  
Jan C. Verdoes ◽  
Peter J. Punt ◽  
Richard Burlingame ◽  
Jeffrey Bartels ◽  
Reijer van Dijk ◽  
...  


protocols.io ◽  
2020 ◽  
Author(s):  
DNA Pipelines ◽  
Benjamin Farr ◽  
Diana Rajan ◽  
Emma Betteridge ◽  
Lesley Shirley ◽  
...  


2016 ◽  
Vol 5 (11) ◽  
pp. 1308-1317 ◽  
Author(s):  
Teng Li ◽  
Jianwen Ye ◽  
Rui Shen ◽  
Yeqing Zong ◽  
Xuejin Zhao ◽  
...  


2022 ◽  
Vol 8 (1) ◽  
Author(s):  
Daniela Gaio ◽  
Kay Anantanawat ◽  
Joyce To ◽  
Michael Liu ◽  
Leigh Monahan ◽  
...  

We developed a low-cost method for the production of Illumina-compatible sequencing libraries that allows up to 14 times more libraries for high-throughput Illumina sequencing to be generated for the same cost. We call this new method Hackflex. The quality of library preparation was tested by constructing libraries from Escherichia coli MG1655 genomic DNA using either Hackflex, standard Nextera Flex (recently renamed as Illumina DNA Prep) or a variation of standard Nextera Flex in which the bead-linked transposase is diluted prior to use. In order to test the library quality for genomes with a higher and a lower G+C content, library construction methods were also tested on Pseudomonas aeruginosa PAO1 and Staphylococcus aureus ATCC 25923, respectively. We demonstrated that Hackflex can produce high-quality libraries and yields a highly uniform coverage, equivalent to the standard Nextera Flex kit. We show that strongly size-selected libraries produce sufficient yield and complexity to support de novo microbial genome assembly, and that assemblies of the large-insert libraries can be much more contiguous than standard libraries without strong size selection. We introduce a new set of sample barcodes that are distinct from standard Illumina barcodes, enabling Hackflex samples to be multiplexed with samples barcoded using standard Illumina kits. Using Hackflex, we were able to achieve a per-sample reagent cost for library prep of A$7.22 (Australian dollars) (US $5.60; UK £3.87, £1=A$1.87), which is 9.87 times lower than the standard Nextera Flex protocol at advertised retail price. An additional simple modification and further simplification of the protocol by omitting the wash step enables a further price reduction to reach an overall 14-fold cost saving. This method will allow researchers to construct more libraries within a given budget, thereby yielding more data and facilitating research programmes where sequencing large numbers of libraries is beneficial.



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