2021
DOI: 10.1093/nargab/lqaa107
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CAMAMED: a pipeline for composition-aware mapping-based analysis of metagenomic data

Abstract: Metagenomics is the study of genomic DNA recovered from a microbial community. Both assembly-based and mapping-based methods have been used to analyze metagenomic data. When appropriate gene catalogs are available, mapping-based methods are preferred over assembly based approaches, especially for analyzing the data at the functional level. In this study, we introduce CAMAMED as a composition-aware mapping-based metagenomic data analysis pipeline. This pipeline can analyze metagenomic samples at both taxonomic … Show more

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Cited by 5 publications
(3 citation statements)
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“…The pipeline was used to check the taxonomic profile of gut microbiota from colorectal adenoma and colorectal carcinoma individuals. The result predicted a significantly changed gut species ratio to 2.67% of the total 374 species [ 44 ]. ezTree, a computational pipeline, is developed to automatically identify single-copy marker genes for a group of genomes and build phylogenetic trees from the marker genes.…”
Section: Road Map To Metagenomics Studymentioning
confidence: 99%
“…The pipeline was used to check the taxonomic profile of gut microbiota from colorectal adenoma and colorectal carcinoma individuals. The result predicted a significantly changed gut species ratio to 2.67% of the total 374 species [ 44 ]. ezTree, a computational pipeline, is developed to automatically identify single-copy marker genes for a group of genomes and build phylogenetic trees from the marker genes.…”
Section: Road Map To Metagenomics Studymentioning
confidence: 99%
“…Compositional Analysis of Single-Cell RNA-seq Data So far, compositional analysis has been an active and ongoing area in metagenomic data (Norouzi-Beirami et al, 2021) and microbiome research (Chen and Li, 2013;Bian et al, 2017;Rivera-Pinto et al, 2018), due to the compositional nature of metagenomic and microbiome data. This is also opens a new perspective on the analysis of single cell RNAseq data.…”
Section: Recover Dropout Events In Single-cell Transcriptome Profilesmentioning
confidence: 99%
“…To our knowledge, there are few broadly accepted standard methods for RNA-seq data generation, processing, and analysis [ 25 , 39 , 40 ]. The most used analysis methods or pipelines can fall into three main categories: (i) mapping sequence reads directly to reference genomes from known pathogens such as Pathoscope [ 41 ] and CAMAMED [ 42 ]; (ii) assembling sequence reads and annotating contigs such as VirFind [ 43 ], VSD toolkit [ 44 ], VirusDetect [ 45 ], and Virtool [ 37 ]; and (iii) read-based taxonomic assignments such as Kaiju [ 46 ], Kraken2 [ 47 ], and Kodoja [ 48 ]. However, these methods or pipelines do not offer an integrated sequence read quality control, read assembly, pathogen reference mapping, and read classification to identify known pathogens and discover novel species, which is a common occurrence during plant virus detection.…”
Section: Introductionmentioning
confidence: 99%