2021
DOI: 10.1111/1755-0998.13340
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User‐friendly bioinformatics pipeline gDAT (graphical downstream analysis tool) for analysing rDNA sequences

Abstract: High‐throughput sequencing (HTS) of multiple organisms in parallel (metabarcoding) has become a routine and cost‐effective method for the analysis of microbial communities in environmental samples. However, careful data treatment is required to identify potential errors in HTS data, and the large volume of data generated by HTS requires in‐house experience with command line tools for downstream analysis. This paper introduces a pipeline that incorporates the most common command line tools into an easy‐to‐use g… Show more

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Cited by 42 publications
(23 citation statements)
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References 79 publications
(142 reference statements)
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“…The 18S rRNA gene animal data were analysed using the gDAT pipeline (Vasar et al., 2021). Demultiplexed paired‐end reads were analysed in the following way: barcode and primer sequences were matched, allowing one mismatch for both pairs.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…The 18S rRNA gene animal data were analysed using the gDAT pipeline (Vasar et al., 2021). Demultiplexed paired‐end reads were analysed in the following way: barcode and primer sequences were matched, allowing one mismatch for both pairs.…”
Section: Methodsmentioning
confidence: 99%
“…ITS PacBio CCS reads (minPasses = 3, MinAccuracy = 0.9) were generated using SMRT Link v.6.0.0.47841. Subsequent quality filtering was performed using pipeCraft v.1.0 (Anslan et al, 2017) The 18S rRNA gene animal data were analysed using the gDAT pipeline (Vasar et al, 2021). Demultiplexed paired-end reads were analysed in the following way: barcode and primer sequences were matched, allowing one mismatch for both pairs.…”
Section: Eukaryotesmentioning
confidence: 99%
“…Bioinformatic data analysis and processing was conducted using the graphical downstream analysis tool (gDAT) for analysing rDNA sequences (Vasar et al, 2021). Raw reads (2X×X2,412,166 reads in total) were demultiplexed and cleaned using a series of bioinformatic steps (see Vasar et al, 2017Vasar et al, , 2021. In short, reads were demultiplexed by checking double barcodes, allowing one mismatch for both reads.…”
Section: Root Chemistrymentioning
confidence: 99%
“…Paired-end Illumina reads were cleaned using gDAT pipeline (Vasar et al 2021). In short, reads were demultiplexed into samples using an 8-bp barcode allowing one mismatch for both forward and reverse reads.…”
Section: Bioinformaticsmentioning
confidence: 99%