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Genome sequencing guide: An introductory toolbox to whole‐genome analysis methods

To fully appreciate genetics, one must understand the link between genotype (DNA sequence) and phenotype (observable characteristics). Advances in high‐throughput genomic sequencing technologies and applications, so‐called “‐omics,” have made genetic sequencing readily available across fields in bio...

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Detalles Bibliográficos
Autores principales: Burian, Alexis N., Zhao, Wufan, Lo, Te‐Wen, Thurtle‐Schmidt, Deborah M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9291972/
https://www.ncbi.nlm.nih.gov/pubmed/34378845
http://dx.doi.org/10.1002/bmb.21561
Descripción
Sumario:To fully appreciate genetics, one must understand the link between genotype (DNA sequence) and phenotype (observable characteristics). Advances in high‐throughput genomic sequencing technologies and applications, so‐called “‐omics,” have made genetic sequencing readily available across fields in biology from applications in non‐traditional study organisms to precision medicine. Thus, understanding these tools is critical for any biologist, especially those early in their career. This comprehensive review discusses the chronological development of different sequencing methods, the bioinformatics steps to analyzing this data, and social and ethical issues raised by these techniques that must be discussed and evaluated, including anticipatory guides and discussion questions for active engagement in the classroom. Additionally, the Supporting Information includes a case study to apply technical and ethical concepts from the text.