Error Prone Whole Genome Amplification
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In bacteria and archaea, the clustered regularly interspaced short palindromic repeats (CRISPR) and associated proteins (Cas) confer adaptive immunity against.
Saccharomyces cerevisiae was transformed for higher ethanol tolerance by error-prone whole genome.
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. or maintenance of transformants with improved acid tolerance. 2.2. Error-prone whole genome. The error-prone whole genome amplification was performed in.
Sep 22, 2015. Whole-genome amplification (WGA) for next-generation sequencing. eMDA and MDA, and the error-prone enzyme used in MALBAC.
Saccharomyces cerevisiae was transformed for higher ethanol tolerance by error-prone whole genome amplification. The resulting PCR products were transformed back to.
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Jun 22, 2017. A new technology, whole genome amplification (WGA), was. of amplification error (false positive rate) and reduced genome coverage. were specific genomic positions that were more prone to cause biases by WGA kits.
Oct 18, 2012. Therefore, the error-prone whole genome amplification technique is a very powerful tool for improving phenotypes of this lactic acid bacterium.
Whole Genome Amplification — Overview – QIAGEN – QIAGEN's whole genome amplification technology solves this problem by providing high yields of whole genomic. which can lead to error-prone amplification.
Jan 16, 2014 · DNA double-strand breaks (DSBs) are harmful lesions leading to genomic instability or diversity. Non-homologous end-joining (NHEJ) is a prominent DSB.
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TruePrime is a novel method for whole-genome amplification from. – Nov 29, 2016. Sequencing of a single-cell genome requires DNA amplification, of the two enzymes thus enables the replacement of the error-prone.
Improved acid tolerance of Lactobacillus pentosus by error-prone whole genome amplification – Acid tolerance of Lactobacillus pentosus ATCC 8041 was improved by error-prone amplification of its genomic.
QIAGEN's whole genome amplification technology solves this problem by. which can lead to error-prone amplification that results in, for example, single.
Apr 15, 2015 · Standard tools for whole-genome alignment, such as MUMmer , can be used to compare assembled genomes to databases of both finished and draft microbial.