Related Experiment Video
Updated: Jun 8, 2025

11:23
Purifying the Impure: Sequencing Metagenomes and Metatranscriptomes from Complex Animal-associated Samples
Published on: December 22, 2014
37.2K
Removal of sequencing adapter contamination improves microbial genome databases
Andrew H Moeller1, Brian A Dillard2, Samantha L Goldman2
1Department of Ecology and Evolutionary Biology, Princeton University, Princeton, NJ, 08540, USA. andrew.moeller@princeton.edu.
BMC Genomics
|November 4, 2024
Summary
Sequencing adapter contamination in microbial genome databases reduces assembly quality. Cleaning these contaminated ends improves the accuracy and contiguity of reference genomes for microbiome research.
Area of Science:
- Microbiology
- Genomics
- Bioinformatics
Background:
- Reference genome databases are crucial for microbiome research.
- Advances in genome assembly have expanded these databases.
- Previous studies have not fully addressed contamination issues.
Purpose of the Study:
- To identify and quantify sequencing adapter contamination in microbial genome databases.
- To assess the impact of contamination on genome assembly quality.
- To improve the accuracy and contiguity of reference microbial genomes.
Main Methods:
- Analysis of published microbial genome databases (human, mouse, cow, pig, fish, honeybee, marine).
- Identification and removal of adapter-contaminated sequence ends.
- Reassembly of contaminated genome sequences.
- Quality assessment of improved assemblies.
Main Results:
- Significant sequencing adapter contamination was found across multiple microbial genome databases.
- Contamination systematically reduced genome assembly accuracy and contiguity.
- Removing contaminated ends and reassembling improved the quality of MGnify reference genomes.
Conclusions:
- Sequencing adapter contamination is a pervasive issue in microbial genome databases.
- Addressing contamination is essential for reliable microbiome research.
- The developed method enhances the quality of publicly available microbial genome assemblies.
Related Concept Videos
Next-generation Sequencing
87.6K
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
87.6K
RNA-seq
9.8K
RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases.
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
9.8K

