2 research outputs found

    Additional file 1 of MGS2AMR: a gene-centric mining of metagenomic sequencing data for pathogens and their antimicrobial resistance profile

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    Additional file 1: Fig. S1. Resolving shortest paths with loops in GFA. Green segment is the start and end of the loop. 1. Loop that begins and ends on the different sides of the start-segment. Resolved by generating two paths (A,B,C,D) and (A,D,C,B). Note that the sequence direction of A differs in two paths. 2. Loop that begins and ends on the same end of the start-segment. Resolved similar to Loop 1, but the direction of A is identical in both paths. 3. Hairpin loop with repeated segments A, B and C. Resolved by creating two paths (A,B,C,D,E,F) and (A,B,C,F,E,D). 4. Hairpin loop with different start- (A) and end- (H) segments. Resolved by removing all path data (G and H) after the repeated segment (C), reducing the problem to the hairpin loop in example 3 with the same solutions: (A,B,C,D,E,F) and (A,B,C,F,E,D). Fig. S2. Example of the evaluation of homology matches. The seed segments of ARG1 and ARG2 both match a reference genome at the same position, indicating they refer to the same ARG. The position of segment 4 in the reference genome does not align with the expected distance from the ARG as represented in the GFA of ARG 1 suggesting it likely represents a false positive match, and therefore will be excluded from further analysis. Fig. S3. Bacteria associated with the 6 bacteria used in validation. This heatmap shows which bacterial sequences (both genome or plasmid) also tend to score high when the known presence is one of the 6 used in validation. It reflects the uncertainty that comes with bacterial calling in metagenomics. Fig. S4. MGS2AMR run time and memory usage for 5 benchmarking samples. All tools were allowed to use up to 8 CPUs. The numbers 1 through 5 refer to the file ID in Table S3. The four main pipeline steps are denoted as follows: A. MetaCherchant (existing tool). B. The MetaCherchant output pre-processing for BLAST (novel R scripts). C. BLAST+ (existing tool) D. ARG annotation (novel R scripts). Note that the large leap in memory for BLASTn is nearly entirely explained by having to load the nucleotide database into memory (~150 GB)

    sj-tiff-1-ini-10.1177_17534259231205959 - Supplemental material for Obesity Alters cytokine signaling and gut microbiome in septic mice

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    Supplemental material, sj-tiff-1-ini-10.1177_17534259231205959 for Obesity Alters cytokine signaling and gut microbiome in septic mice by Lauren Bodilly, Lauren Williamson, Patrick Lahni and Matthew N. Alder, David B. Haslam, Jennifer M. Kaplan in Innate Immunity</p
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