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This eBook is a collection of articles from a Frontiers Research Topic. Frontiers Research Topics are very popular trademarks of the Frontiers Journals Series: they are collections of at least ten articles, all centered on a particular subject. With their unique mix of varied contributions from Original Research to Review Articles, Frontiers Research Topics unify the most influential researchers, the latest key findings and historical advances in a hot research area! Find out more on how to host your own Frontiers Research Topic or contribute to one as an author by contacting the Frontiers Editorial Office: frontiersin.org/about/contact

toxicogenomics --- Gene Expression --- Toxicology --- chemicals --- exposures --- mode of action --- integration --- bioinformatics --- gene regulatory network --- Next-generation sequencing

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This eBook is a collection of articles from a Frontiers Research Topic. Frontiers Research Topics are very popular trademarks of the Frontiers Journals Series: they are collections of at least ten articles, all centered on a particular subject. With their unique mix of varied contributions from Original Research to Review Articles, Frontiers Research Topics unify the most influential researchers, the latest key findings and historical advances in a hot research area! Find out more on how to host your own Frontiers Research Topic or contribute to one as an author by contacting the Frontiers Editorial Office: frontiersin.org/about/contact

Science: general issues --- Medical genetics --- toxicogenomics --- Gene Expression --- Toxicology --- chemicals --- exposures --- mode of action --- integration --- bioinformatics --- gene regulatory network --- Next-generation sequencing

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This eBook is a collection of articles from a Frontiers Research Topic. Frontiers Research Topics are very popular trademarks of the Frontiers Journals Series: they are collections of at least ten articles, all centered on a particular subject. With their unique mix of varied contributions from Original Research to Review Articles, Frontiers Research Topics unify the most influential researchers, the latest key findings and historical advances in a hot research area! Find out more on how to host your own Frontiers Research Topic or contribute to one as an author by contacting the Frontiers Editorial Office: frontiersin.org/about/contact

Science: general issues --- Medical genetics --- antibiotic resistance --- next generation sequencing --- mobile genetic element --- horizontal gene transfer --- Mutation Rate --- infectious diseases --- resistome --- New Antibiotic Target --- Direct Evolution Experiment --- antibiotic resistance --- next generation sequencing --- mobile genetic element --- horizontal gene transfer --- Mutation Rate --- infectious diseases --- resistome --- New Antibiotic Target --- Direct Evolution Experiment

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The contribution of genomic variants to the aetiopathogenesis of both paediatric and adult neurological disease is being increasingly recognized. The use of next-generation sequencing has led to the discovery of novel neurodevelopmental disorders, as exemplified by the deciphering developmental disorders (DDD) study, and provided insight into the aetiopathogenesis of common adult neurological diseases. Despite these advances, many challenges remain. Correctly classifying the pathogenicity of genomic variants from amongst the large number of variants identified by next-generation sequencing is recognized as perhaps the major challenge facing the field. Deep phenotyping (e.g., imaging, movement analysis) techniques can aid variant interpretation by correctly classifying individuals as affected or unaffected for segregation studies. The lack of information on the clinical phenotype of novel genetic subtypes of neurological disease creates limitations for genetic counselling. Both deep phenotyping and qualitative studies can capture the clinical and patient’s perspective on a disease and provide valuable information. This Special Issue aims to highlight how next-generation sequencing techniques have revolutionised our understanding of the aetiology of brain disease and describe the contribution of deep phenotyping studies to a variant interpretation and understanding of natural history.

polymicrogyria --- n/a --- neurodegenerative disease --- next generation sequencing (NGS) --- inborn error of metabolism --- genetic biomarker --- deep learning --- TUBA1A --- Alzheimer’s disease (AD) --- ataxia --- risk prediction --- p.(Arg2His) --- movement science --- tubulin --- R2H --- diagnosis --- machine learning --- metal storage disorders --- amyotrophic lateral sclerosis (ALS) --- glucocerebrosidase --- Parkinsonism --- cerebellar hypoplasia --- Gaucher disease --- disease phenotyping --- tubulinopathy --- Parkinson’s disease (PD) --- dementia --- Parkinson’s disease --- Neurogenetics. --- Nervous system --- Genetics --- Neurosciences --- Genetic aspects --- Alzheimer's disease (AD) --- Parkinson's disease (PD) --- Parkinson's disease

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PacBio’s single-molecule real-time (SMRT) sequencing technology offers important advantages over the short-read DNA sequencing technologies that currently dominate the market. This includes exceptionally long read lengths (20 kb or more), unparalleled consensus accuracy, and the ability to sequence native, non-amplified DNA molecules. From fungi to insects to humans, long reads are now used to create highly accurate reference genomes by de novo assembly of genomic DNA and to obtain a comprehensive view of transcriptomes through the sequencing of full-length cDNAs. Besides reducing biases, sequencing native DNA also permits the direct measurement of DNA base modifications. Therefore, SMRT sequencing has become an attractive technology in many fields, such as agriculture, basic science, and medical research. The boundaries of SMRT sequencing are continuously being pushed by developments in bioinformatics and sample preparation. This book contains a collection of articles showcasing the latest developments and the breadth of applications enabled by SMRT sequencing technology.

n/a --- Cladobotryum protrusum --- allele-specific analysis --- low-input DNA --- full length RNAseq --- de novo genome assembly --- de novo assembly --- human reference genome --- Tricoplusia ni --- PacBio single molecule real-time sequencing --- secondary metabolite --- protein isoforms --- bone marrow cell subpopulations --- DNA methylation --- mycoparasite --- human whole-genome sequencing --- GRCh38 --- SMRT sequencing --- cytochrome P450 enzyme (CYP) --- mRNA isoforms --- next generation sequencing --- cobweb disease --- Swedish population --- mosquito --- long-read SMRT sequencing --- whole genome sequencing --- terpenoid --- insect genome --- optical mapping --- Gloeostereum incarnatum --- population sequencing --- statistical methods --- gene expression --- single molecule real-time sequencing --- PacBio