Furman University Scholar Exchange - South Carolina Junior Academy of Science: Using bioinformatics to probe gut microbial taxonomic data.
 

Using bioinformatics to probe gut microbial taxonomic data.

School Name

Socastee High School

Grade Level

12th Grade

Presentation Topic

Microbiology

Presentation Type

Non-Mentored

Abstract

This research project investigates a subset (n = 17) of publicly available human gut microbiota metagenomes from the American Gut Project to explore the prevalence of gut bacterial taxa associated with neurological dysfunction. Specifically, the sample metadata category of body mass index (BMI) is examined to determine if gut microbiota associated with neurological dysfunction exhibit differentially partitioned abundance patterns among BMI categories. A bioinformatic pipeline was used to analyze the metagenomic sequence data and to generate comprehensive taxonomic profiles examining both within-sample alpha diversity and between-sample beta diversity. This pipeline begins with data filtering using DADA2 for Illumina amplicon detection and correlation, then analyzing sample composition through PERMANOVA in relation to categorical metadata, and ultimately assessing beta diversity to determine statistical separation between gut microbiota communities of high versus normal BMI individuals. Although a statistical difference was not found between samples of normal and high BMI individuals, but certain bacterial taxa are found in greater abundance within the different BMI categories, meriting further study.

Location

PENNY 311

Start Date

4-5-2025 9:30 AM

Presentation Format

Oral Only

Group Project

No

COinS
 
Apr 5th, 9:30 AM

Using bioinformatics to probe gut microbial taxonomic data.

PENNY 311

This research project investigates a subset (n = 17) of publicly available human gut microbiota metagenomes from the American Gut Project to explore the prevalence of gut bacterial taxa associated with neurological dysfunction. Specifically, the sample metadata category of body mass index (BMI) is examined to determine if gut microbiota associated with neurological dysfunction exhibit differentially partitioned abundance patterns among BMI categories. A bioinformatic pipeline was used to analyze the metagenomic sequence data and to generate comprehensive taxonomic profiles examining both within-sample alpha diversity and between-sample beta diversity. This pipeline begins with data filtering using DADA2 for Illumina amplicon detection and correlation, then analyzing sample composition through PERMANOVA in relation to categorical metadata, and ultimately assessing beta diversity to determine statistical separation between gut microbiota communities of high versus normal BMI individuals. Although a statistical difference was not found between samples of normal and high BMI individuals, but certain bacterial taxa are found in greater abundance within the different BMI categories, meriting further study.