2021
DOI: 10.1186/s12864-021-07405-8
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GalaxyTrakr: a distributed analysis tool for public health whole genome sequence data accessible to non-bioinformaticians

Abstract: Background Processing and analyzing whole genome sequencing (WGS) is computationally intense: a single Illumina MiSeq WGS run produces ~ 1 million 250-base-pair reads for each of 24 samples. This poses significant obstacles for smaller laboratories, or laboratories not affiliated with larger projects, which may not have dedicated bioinformatics staff or computing power to effectively use genomic data to protect public health. Building on the success of the cloud-based Galaxy bioinformatics plat… Show more

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Cited by 60 publications
(45 citation statements)
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“…The first study ( 16 ) examined 92 strains from 76 patient and food samples by SNP calling and phylogenetic analysis. SNP calling was done by mapping sequencing reads to reference genomes using GalaxyTrakr's pipeline of the Center for Food Safety and Applied Nutrition (CFSAN) ( 18 ) and with NCBI Pathogen Detection, which uses genome assemblies and performs kmer-based clustering followed by 50-SNP single linkage clustering. Of the examined strains, 24 were from sporadic samples, and 16 were cultured from the same samples; hence, they were excluded from our reanalysis.…”
Section: Resultsmentioning
confidence: 99%
“…The first study ( 16 ) examined 92 strains from 76 patient and food samples by SNP calling and phylogenetic analysis. SNP calling was done by mapping sequencing reads to reference genomes using GalaxyTrakr's pipeline of the Center for Food Safety and Applied Nutrition (CFSAN) ( 18 ) and with NCBI Pathogen Detection, which uses genome assemblies and performs kmer-based clustering followed by 50-SNP single linkage clustering. Of the examined strains, 24 were from sporadic samples, and 16 were cultured from the same samples; hence, they were excluded from our reanalysis.…”
Section: Resultsmentioning
confidence: 99%
“…GalaxyTrakr is an instance of Galaxy 11 that was developed by the FDA as a bioinformatics platform for use by United States public health laboratories. However, it is particularly advantageous for educational use, as the computational tools included are only those typically used for studying microbial genomes in general, particularly those of pathogens (Gangiredla et al, 2021). After they assembled, annotated, and serotyped their isolate genomes, students were then asked to pursue specific questions and hypotheses related to genes and gene functional categories of interest in their isolates, including those relating to antibiotic resistance, virulence, phages, plasmids, transposons, etc.…”
Section: Discussionmentioning
confidence: 99%
“…Sequence data were processed according to the pipeline shown in Figure 1B. Bioinformatic processing and analyses were done in GalaxyTrakr (Gangiredla et al, 2021) or using the command line interface on a computer with an Ubuntu 16.04 LTS operating system. Short read data were quality checked using FastQC 4 version 0.72 or 0.69.…”
Section: Sequence Data Quality Control and Analysismentioning
confidence: 99%
See 1 more Smart Citation
“…Libraries were built using the Nextera XT DNA Library Preparation Kit (Illumina, Milan, Italy) and sequenced on Illumina MiSeq Platform which generates tagged 250 bp paired end reads. Unless otherwise indicated, all subsequent genomic analyses were performed on Galaxy Trakr platform ( Gangiredla et al, 2021 ). After performing a quality cleaning through TRIMMOMATIC, reads were de novo assembled using Shovill v.1.0.4, a standardized and fully automatic open-source pipeline for bacterial genome assembly.…”
Section: Methodsmentioning
confidence: 99%