18 research outputs found

    Core-gene clusters

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    Gene clusters of the 2,138 <i>Salmonella</i> Core genes for all 221 genomes in .tar.gz forma

    Output of RMFinder

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    The output information from Restriction-ModificationFinder for each of the 221 <i>Salmonella</i> genome

    Pan-gene clusters

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    Gene clusters of the 16,375 <i>Salmonella</i> Pan genes for all 221 genomes in .tar.gz forma

    A schematic flowchart for processing of paired-end sequences with MGmapper.

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    <p>MGmapper processes fastq reads in four steps. These consist of: (I) Trimming and mapping reads against a phiX bacteriophage to remove potential positive control reads. (II) Mapping to specified reference databases, post-processing of BWA-mem alignments to remove reads with low alignment score or insufficient alignment coverage. (III) Identification of best hits in <i>bestmode</i>: Assignment of a read-pairs to only one specific reference sequence based on the highest sum of alignment scores. In <i>fullmode</i>, assigned a read-pair to a reference sequence even if a higher alignment score is found when mapping to another reference sequence database. This will provide best target match, considering only the sequences present in one particular reference database. (IV) Compilation of abundance statistics, read and nucleotide counts, depth, coverage, and summary reports.</p
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