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Long-read sequencing to understand genome biology and cell function.
Kraft, Florian; Kurth, Ingo.
Affiliation
  • Kraft F; Institute of Human Genetics, Medical Faculty, RWTH Aachen University, Aachen, Germany. Electronic address: fkraft@ukaachen.de.
  • Kurth I; Institute of Human Genetics, Medical Faculty, RWTH Aachen University, Aachen, Germany. Electronic address: ikurth@ukaachen.de.
Int J Biochem Cell Biol ; 126: 105799, 2020 09.
Article in En | MEDLINE | ID: mdl-32629027
ABSTRACT
Determining the sequence of DNA and RNA molecules has a huge impact on the understanding of cell biology and function. Recent advancements in next-generation short-read sequencing (NGS) technologies, drops in cost and a resolution down to the single-cell level shaped our current view on genome structure and function. Third-generation sequencing (TGS) methods further complete the knowledge about these processes based on long reads and the ability to analyze DNA or RNA at single molecule level. Long-read sequencing provides additional possibilities to study genome architecture and the composition of highly complex regions and to determine epigenetic modifications of nucleotide bases at a genome-wide level. We discuss the principles and advancements of long-read sequencing and its applications in genome biology.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cells / Genomics / High-Throughput Nucleotide Sequencing Limits: Animals / Humans Language: En Journal: Int J Biochem Cell Biol Journal subject: BIOQUIMICA Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cells / Genomics / High-Throughput Nucleotide Sequencing Limits: Animals / Humans Language: En Journal: Int J Biochem Cell Biol Journal subject: BIOQUIMICA Year: 2020 Document type: Article