Related Experiment Video
Updated: Oct 11, 2025

11:59
Competitive Genomic Screens of Barcoded Yeast Libraries
Published on: August 11, 2011
18.5K
An update on DNA barcoding: low species coverage and numerous unidentified sequences
Shiyang Kwong1, Amrita Srivathsan1, Rudolf Meier1,2
1Department of Biological Sciences.
Cladistics : the International Journal of the Willi Hennig Society
|December 3, 2021
Summary
DNA barcoding for multicellular animals shows sparse species coverage despite significant funding. Most public DNA barcodes are not identified to species, hindering biodiversity assessment.
Area of Science:
- Genomics
- Biodiversity Science
- Bioinformatics
Background:
- The DNA barcoding initiative, established in 2003, aims to catalog species using standardized genetic markers.
- Significant funding has been invested, yet comprehensive species coverage remains a challenge.
Purpose of the Study:
- To assess the current species coverage of DNA barcoding in multicellular animals.
- To compare data availability between public repositories (GenBank) and specialized databases (BOLD).
Main Methods:
- Comparative analysis of DNA sequence data from GenBank and the Barcode of Life Database (BOLD) as of January 2012.
- Evaluation of species identification levels and data provenance for deposited sequences.
Main Results:
- GenBank contained COI sequences for approximately 60,000 species, while BOLD reported 150,000, with the discrepancy attributed to unpublished data in BOLD.
- Overall species coverage is sparse, with low growth rates and a linear accumulation curve for Metazoa.
- A significant portion (73%) of GenBank data originated from non-barcoding projects, and 74% of DNA barcodes lacked species-level identification.
Conclusions:
- Despite substantial investment, DNA barcoding coverage for multicellular animals remains limited.
- Data quality and identification accuracy in public databases present challenges for biodiversity research.
- Targeted barcoding campaigns show better coverage but still fall short of campaign goals.
Related Concept Videos
Evolutionary Relationships through Genome Comparisons
6.4K
Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
6.4K
Modern Molecular Taxonomy
250
Advancements in molecular biology have revolutionized the identification and characterization of bacteria, with multiple methods leveraging DNA sequencing for enhanced precision. As sequencing technologies improve and costs decline, these approaches are increasingly used in clinical, environmental, and evolutionary studies.Multilocus Sequence Typing (MLST) examines several housekeeping genes, essential chromosomal genes encoding cellular functions, to distinguish strains. Approximately...
250
RNA-seq
10.5K
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...
10.5K
Next-generation Sequencing
93.9K
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....
93.9K
Sanger Sequencing
761.1K
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
761.1K

