Next-Generation Sequencing Techniques: Solutions to Biological Problems

A special issue of Biology (ISSN 2079-7737). This special issue belongs to the section "Genetics and Genomics".

Deadline for manuscript submissions: closed (31 December 2023) | Viewed by 2704

Special Issue Editors

Department of Pathobiology, College of Veterinary Medicine, Auburn University, Auburn, AL 36849, USA
Interests: comparative genomics; evolutionary genomics; metagenomics; reproduction
Special Issues, Collections and Topics in MDPI journals
School of Fisheries, Aquaculture and Aquatic Sciences, Auburn University, Auburn, AL 36849, USA
Interests: fish breeding and physiology; genome editing; transgenics; applied bioinformatics and genomics; gene function and characterization; mucosal immunity
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues, 

Since 2005, when next-generation sequencing (NGS) technologies became available to the public, they have changed all areas of biology. The sequencing quality and yield are constantly improving, and the costs continue to decrease. During the Human Genomic Project between 1990 and 2003, up to USD 3 billion was spent to sequence and assemble the 3 billion base-pair human genome. However, one gigabase of sequences can currently be generated for less than $10 on an Illumina NovaSeq 6000 instrument. NGS techniques have been widely applied in fundamental research, such as characterizing the genome, gene expression, and epigenetic profiles; in agricultural research, such as genome-assisted breeding to develop new varieties, stocks, and breeds; and in genome/transcriptome analyses to control pathogens and pests. The massive parallel NGS accelerates biomedical research and large-scale studies, such as genome-wide association studies (GWASs), the Cancer Genome Atlas (TCGA), and the Genotype-Tissue Expression Project (GTEx), which would not be possible without NGS. Personalized medicine relies on NGS to discover disease-causing genes and pharmacogenomic loci. NGS has also significantly advanced the environment, soil, and animal microbiota research through the metagenomic characterization of unculturable microbes. Accurate long-read sequencing, single-cell sequencing, and spatial sequencing have recently brought NGS applications to the next level. NGS technology provides unprecedented capability to tackle biological questions. In this Special Issue, we invite articles using NGS technologies to address all kinds of biological questions, including but not limited to DNA sequencing, RNA sequencing, exome sequencing, single-cell sequencing, DNA methylome sequencing, ChIP-seq, ATAC-seq, 16S/18S and whole-genome metagenomic sequencing, and metatranscriptomic sequencing.

Dr. Xu Wang
Dr. Baofeng Su
Guest Editors

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Keywords

  • next-generation sequencing genome
  • gene expression
  • epigenetic profile
  • genome-assisted breeding
  • long-read sequencing
  • single-cell spatial sequencing
  • whole-genome metagenomic sequencing

Published Papers (2 papers)

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Research

14 pages, 2217 KiB  
Article
Diet Diversity of the Fluviatile Masu Salmon, Oncorhynchus masou (Brevoort 1856) Revealed via Gastrointestinal Environmental DNA Metabarcoding and Morphological Identification of Contents
by Lijuan Li, Xuwang Yin, Qianruo Wan, Dilina Rusitanmu and Jie Han
Biology 2024, 13(2), 129; https://doi.org/10.3390/biology13020129 - 18 Feb 2024
Viewed by 1144
Abstract
Masu salmon, Oncorhynchus masou (Brevoort 1856), a commercially important fish species endemic to the North Pacific Ocean, attained national second-level protected animal status in China in 2021. Despite this recognition, knowledge about the trophic ecology of this fish remains limited. This study investigated [...] Read more.
Masu salmon, Oncorhynchus masou (Brevoort 1856), a commercially important fish species endemic to the North Pacific Ocean, attained national second-level protected animal status in China in 2021. Despite this recognition, knowledge about the trophic ecology of this fish remains limited. This study investigated the diet diversity of fluviatile Masu salmon in the Mijiang River, China, utilizing the gastrointestinal tract environmental DNA (GITeDNA) metabarcoding and morphological identification. The results revealed a diverse prey composition, ranging from terrestrial and aquatic invertebrates to small fishes. The fluviatile Masu salmon in general consumed noteworthily more aquatic prey than terrestrial prey. There were much more prey taxa and a higher diet diversity detected by GITeDNA metabarcoding than by morphological identification. GITeDNA metabarcoding showed that larger and older Masu salmon consumed significantly more terrestrial insects than aquatic prey species did, with 7366 verses 5012 sequences in the group of ≥20 cm, 9098 verses 4743 sequences in the group of ≥100 g and 11,540 verses 729 sequences in the group of age 3+. GITeDNA metabarcoding also showed size- and age-related diet diversity, indicating that the dietary niche breadth and trophic diversity of larger and older Masu salmon increased with food resources expanding to more terrestrial prey. Terrestrial invertebrates of riparian habitats play a vital role in the diet of fluviatile Masu salmon, especially larger individuals, highlighting their importance in connecting aquatic and terrestrial food webs. Conservation plans should prioritize the protection and restoration of riparian habitats. This study advocates the combined use of GITeDNA metabarcoding and morphological observation for a comprehensive understanding of fish diet diversity. Full article
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16 pages, 11327 KiB  
Article
Transcription and Metabolic Profiling Analysis of Three Discolorations in a Day of Hibiscus mutabilis
by Zhangshun Zhu, Xinmei Zeng, Xiaoqing Shi, Jiao Ma, Xiaoli Liu and Qiang Li
Biology 2023, 12(8), 1115; https://doi.org/10.3390/biology12081115 - 10 Aug 2023
Cited by 2 | Viewed by 1021
Abstract
In this study, we used combined transcriptomics and metabolomics to analyze the H. mutabilis cultivar’s genetic and physiological mechanisms during three flower color transition periods (from white to pink, then from pink to red) within the span of one day. As a result, [...] Read more.
In this study, we used combined transcriptomics and metabolomics to analyze the H. mutabilis cultivar’s genetic and physiological mechanisms during three flower color transition periods (from white to pink, then from pink to red) within the span of one day. As a result, 186 genes were found to be significantly increased with the deepening of the H. mutabilis flower color; these genes were mainly involved in the expression of peroxidase 30, zinc finger protein, phosphate transporter PHO1, etc. In contrast, 298 genes were significantly downregulated with the deepening of H. mutabilis flower color, including those involved in the expression of probable O-methyltransferase 3, copper binding protein 9, and heat stress transcription factor A-6b. Some genes showed differential expression strategies as the flower color gradually darkened. We further detected 19 metabolites that gradually increased with the deepening of the H. mutabilis flower color, including L-isoleucine, palmitic acid, L-methionine, and (+)-7-isonitrobenzene. The content of the metabolite hexadecanedioate decreased with the deepening of the H. mutabilis flower color. Combined transcriptomics and metabolomics revealed that the metabolic pathways, including those related to anthocyanin biosynthesis, cysteine and methionine metabolism, and sulfur metabolism, appear to be closely related to H. mutabilis flower color transition. This study served as the first report on the genetic and physiological mechanisms of short-term H. mutabilis flower color transition and will promote the molecular breeding of ornamental cultivars of H. mutabilis. Full article
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