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CAIM: Coverage-based Analysis for Identification of Microbiome
by
Kandel, Sangam
, Jenjaroenpun, Piroon
, Chuaypen, Natthaya
, Kusonmano, Kanthida
, Krulilung, Alongkorn
, Pomyen, Yotsawat
, Wongsurawat, Thidathip
, Nookaew, Intawat
, Acheampong, Daniel A
, Kunadirek, Pattapon
in
Bioinformatics
2024
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CAIM: Coverage-based Analysis for Identification of Microbiome
by
Kandel, Sangam
, Jenjaroenpun, Piroon
, Chuaypen, Natthaya
, Kusonmano, Kanthida
, Krulilung, Alongkorn
, Pomyen, Yotsawat
, Wongsurawat, Thidathip
, Nookaew, Intawat
, Acheampong, Daniel A
, Kunadirek, Pattapon
in
Bioinformatics
2024
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Do you wish to request the book?
CAIM: Coverage-based Analysis for Identification of Microbiome
by
Kandel, Sangam
, Jenjaroenpun, Piroon
, Chuaypen, Natthaya
, Kusonmano, Kanthida
, Krulilung, Alongkorn
, Pomyen, Yotsawat
, Wongsurawat, Thidathip
, Nookaew, Intawat
, Acheampong, Daniel A
, Kunadirek, Pattapon
in
Bioinformatics
2024
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CAIM: Coverage-based Analysis for Identification of Microbiome
Journal Article
CAIM: Coverage-based Analysis for Identification of Microbiome
2024
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Overview
Accurate taxonomic profiling of microbial taxa in a metagenomic sample is vital to gain insights into microbial ecology. Recent advancements in sequencing technologies have contributed tremendously toward understanding these microbes at species resolution through a whole shotgun metagenomic (WMS) approach. In this study, we developed a new bioinformatics tool, CAIM, for accurate taxonomic classification and quantification within both long- and short-read metagenomic samples using an alignment-based method. CAIM depends on two different containment techniques to identify species in metagenomic samples using their genome coverage information to filter out false positives rather than the traditional approach of relative abundance. In addition, we propose a nucleotide-count based abundance estimation, which yield lesser root mean square error than the traditional read-count approach. We evaluated the performance of CAIM on 28 metagenomic mock communities and 2 synthetic datasets by comparing it with other top-performing tools. CAIM maintained a consitently good performance across datasets in identifying microbial taxa and in estimating relative abundances than other tools. CAIM was then applied to a real dataset sequenced on both Nanopore (with and without amplification) and Illumina sequencing platforms and found high similality of taxonomic profiles between the sequencing platforms. Lastly, CAIM was applied to fecal shotgun metagenomic datasets of 232 colorectal cancer patients and 229 controls obtained from 4 different countries and primary 44 liver cancer patients and 76 controls. The predictive performance of models using the genome-coverage cutoff was better than those using the relative-abundance cutoffs in discriminating colorectal cancer and primary liver cancer patients from healthy controls with a highly confident species markers.
Publisher
Cold Spring Harbor Laboratory
Subject
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