2012
DOI: 10.14806/ej.18.b.551
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BioQuery-ASP: querying biomedical databases and ontologies using answer set programming

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Cited by 5 publications
(3 citation statements)
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“…The CCS reads were processed with DADA2 software packages (16S rRNA gene and ITS specific workflow) (version 1.8) [ 58 ], and analyzed with phyloseq for alpha and beta diversity (version 1.25.2) [ 59 ]. For 16s rRNA gene CCS data, the DADA2 workflow follows primer trimming, quality filtering, and de-replication.…”
Section: Methodsmentioning
confidence: 99%
“…The CCS reads were processed with DADA2 software packages (16S rRNA gene and ITS specific workflow) (version 1.8) [ 58 ], and analyzed with phyloseq for alpha and beta diversity (version 1.25.2) [ 59 ]. For 16s rRNA gene CCS data, the DADA2 workflow follows primer trimming, quality filtering, and de-replication.…”
Section: Methodsmentioning
confidence: 99%
“…For the fungal data analysis, we followed the ITS-speci c variation of the DADA2 package. In the fungal DADA2 work ow, after orienting the primers, we used a specialized primer/adapter removal tool "cutadapt" [53]. After primer removal, the steps are quality ltering, dereplication, inferring ASVs after error learning, and nally removing chimeras.…”
Section: Discussionmentioning
confidence: 99%
“…The libraries were denatured using Denature and Dilute Libraries for HiSeq Clustering protocol and sequenced in Rapid Run mode by Genotek (Russia) using Illumina HiSeq 2500 (Illumina, USA) at a read length of 150 paired-end bp. Adaptors and nucleotides with a Phred score <30 were removed using Cutadapt v2.10 (error-rate = 0.1). Clean reads were mapped to the genome of R. rhodochrous M8 (GCF_001890475.2 in RefSeq database) using BWA-MEM v 0.7.17 (− k = 30).…”
Section: Methodsmentioning
confidence: 99%