Evaluating coverage bias in next-generation sequencing of Escherichia coli

Evaluating coverage bias in next-generation sequencing of Escherichia coli

4.6
(676)
Write Review
More
$ 22.00
Add to Cart
In stock
Description

Whole-genome sequencing is essential to many facets of infectious disease research. However, technical limitations such as bias in coverage and tagmentation, and difficulties characterising genomic regions with extreme GC content have created significant obstacles in its use. Illumina has claimed that the recently released DNA Prep library preparation kit, formerly known as Nextera Flex, overcomes some of these limitations. This study aimed to assess bias in coverage, tagmentation, GC content, average fragment size distribution, and de novo assembly quality using both the Nextera XT and DNA Prep kits from Illumina. When performing whole-genome sequencing on Escherichia coli and where coverage bias is the main concern, the DNA Prep kit may provide higher quality results; though de novo assembly quality, tagmentation bias and GC content related bias are unlikely to improve. Based on these results, laboratories with existing workflows based on Nextera XT would see minor benefits in transitioning to the DNA Prep kit if they were primarily studying organisms with neutral GC content.

Evaluating coverage bias in next-generation sequencing of Escherichia coli

Solid-phase enzyme catalysis of DNA end repair and 3′ A-tailing reduces GC- bias in next-generation sequencing of human genomic DNA

Mapping and SNP Calling Tutorial

Illumina blind spots in M. tuberculosis WGS. (a) Distribution of blind

Evaluating coverage bias in next-generation sequencing of Escherichia coli

Frontiers German-Wide Interlaboratory Study Compares Consistency, Accuracy and Reproducibility of Whole-Genome Short Read Sequencing

Blind spot prevalence across all instruments, library preps and their

Frontiers The efficiency of Nextera XT tagmentation depends on G and C bases in the binding motif leading to uneven coverage in bacterial species with low and neutral GC-content

Sequencing biases of low-GC regions and assembly quality of entire

PDF] Summarizing and correcting the GC content bias in high-throughput sequencing

Frontiers A Comparative Overview of Epigenomic Profiling Methods

Understanding and controlling for sample and platform biases in NGS assays

Library preparation for next generation sequencing: A review of automation strategies - ScienceDirect

Measuring sequencer size bias using REcount: a novel method for highly accurate Illumina sequencing-based quantification, Genome Biology

DNA sequencing - Wikipedia