2014
DOI: 10.1186/2049-2618-2-6
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An improved dual-indexing approach for multiplexed 16S rRNA gene sequencing on the Illumina MiSeq platform

Abstract: BackgroundTo take advantage of affordable high-throughput next-generation sequencing technologies to characterize microbial community composition often requires the development of improved methods to overcome technical limitations inherent to the sequencing platforms. Sequencing low sequence diversity libraries such as 16S rRNA amplicons has been problematic on the Illumina MiSeq platform and often generates sequences of suboptimal quality.ResultsHere we present an improved dual-indexing amplification and sequ… Show more

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Cited by 1,388 publications
(1,069 citation statements)
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References 14 publications
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“…Shortly, genomic DNA was extracted according to Qiamp Fast DNA Stool extraction kit (Qiagen) and the V3-V4 region of bacterial 16srRNA genes was amplified with the NEBNext Q5 Hot Start Hifi PCR Master Mix (NEB) using a dual-index strategy (15). The amplified fragments were purified with AMPure XP Beads (Beckmann Coulter Genomics), combined and analyzed by '2 × 300 bp paired-end' sequencing using a Illumina MiSeq device.…”
Section: Methodsmentioning
confidence: 99%
“…Shortly, genomic DNA was extracted according to Qiamp Fast DNA Stool extraction kit (Qiagen) and the V3-V4 region of bacterial 16srRNA genes was amplified with the NEBNext Q5 Hot Start Hifi PCR Master Mix (NEB) using a dual-index strategy (15). The amplified fragments were purified with AMPure XP Beads (Beckmann Coulter Genomics), combined and analyzed by '2 × 300 bp paired-end' sequencing using a Illumina MiSeq device.…”
Section: Methodsmentioning
confidence: 99%
“…DNA obtained from 90 environmental samples was amplified using primers targeting the V3-V4 region of the 16S rRNA gene (F319 5 ′ -ACTCCTACGGGAGGCAGCAG-3 ′ , R806 5 ′ -GGACTACHVGGGTWTCTAAT-3 ′ , Fadrosh et al, 2014). We used a dual multiplexing approach and a "heterogeneity spacer" of 0-3 bp length between the Illumina adapter and the forward/reverse primer sequence to increase read quality.…”
Section: Dna Extraction and 16s Rrna Gene Sequencingmentioning
confidence: 99%
“…We obtained a clean data of sequence reads by pre-processing the removal of the primer sequence; truncation of sequence reads not having an average quality of 20 over a 30-bp sliding window based on the phred algorithm; and removal of trimmed reads having o75% of their original length, as well as its paired read (Fadrosh et al, 2014). These stringent criteria resulted in nearly 94% of the reads being retained.…”
Section: Dsrna Synthesis and Delivery By Injectionmentioning
confidence: 99%