Related Experiment Video
Updated: Sep 6, 2025

11:13
RNA-Seq Analysis of Differential Gene Expression in Electroporated Chick Embryonic Spinal Cord
Published on: November 1, 2014
14.7K
Transcript- and annotation-guided genome assembly of the European starling.
Katarina C Stuart1, Richard J Edwards2, Yuanyuan Cheng3
1Evolution & Ecology Research Centre, School of Biological, Earth and Environmental Sciences, UNSW Sydney, Sydney, New South Wales, Australia.
Molecular Ecology Resources
|June 28, 2022
Summary
We present new European starling genome assemblies to aid population genetics and evolutionary studies. These resources will help researchers understand this invasive yet declining avian species.
Area of Science:
- Genomics
- Avian Biology
- Bioinformatics
Background:
- The European starling (Sturnus vulgaris) is a globally invasive species facing population declines in its native range.
- Understanding its genome is crucial for ecological and evolutionary research.
Purpose of the Study:
- To generate high-quality reference genome assemblies for the European starling.
- To provide genomic resources for population genetic and evolutionary characterization.
- To introduce new bioinformatic tools for assessing genome assembly quality.
Main Methods:
- Generated a long-read genome assembly (S. vulgaris vAU) using linked-reads, Nanopore sequencing, and PacBio Iso-Seq.
- Created a short-read genome assembly (S. vulgaris vNA).
- Scaffolded the vAU assembly using the zebra finch genome and annotated genes using species-specific transcripts.
Main Results:
- Produced a 1050 Mb European starling genome assembly (vAU) with high contiguity and completeness (94.6% BUSCO).
- Successfully assigned 98.6% of the assembly to 32 putative chromosomes.
- Demonstrated the utility of PacBio Iso-Seq data and introduced new tools (saaga, buscomp) for assembly validation and comparison.
Conclusions:
- The new genomic resources significantly enhance the study of European starling populations and evolution.
- The developed bioinformatic tools improve genome assembly assessment and quality control.
- These advancements facilitate future global genomic and transcriptomic analyses of this ecologically significant species.
More Related Videos
Related Concept Videos
Genome Annotation and Assembly
19.3K
The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
19.3K
RNA-seq
10.4K
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...
10.4K
Genomic DNA in Eukaryotes
47.6K
Eukaryotes have large genomes compared to prokaryotes. To fit their genomes into a cell, eukaryotic DNA is packaged extraordinarily tightly inside the nucleus. To achieve this, DNA is tightly wound around proteins called histones, which are packaged into nucleosomes that are joined by linker DNA and coil into chromatin fibers. Additional fibrous proteins further compact the chromatin, which is recognizable as chromosomes during certain phases of cell division.
47.6K
Protein Complex Assembly
2.1K
2.1K
Next-generation Sequencing
92.5K
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....
92.5K

