About this Research Topic
“A Year in Review: Discussions in Genomic Assay Technology” is part of a wider series of Research Topics across Frontiers in Genetics, hosted by our Specialty Chief Editors.
This Research Topic aims to spark discussion around popular articles from 2022 in Genomic Assay Technology. This field is continuously evolving; therefore, we are seeking to understand developments and perspectives on articles that have attracted attention throughout the year.
The chosen manuscripts are:
Full-Length Spatial Transcriptomics Reveals the Unexplored Isoform Diversity of the Myocardium Post-MI
Combinatorial and Machine Learning Approaches for Improved Somatic Variant Calling from Formalin-Fixed Paraffin-Embedded Genome Sequence Data
Cell-Based NIPT Detects 47,XXY Genotype in a Twin Pregnancy
Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to Genotyping Arrays in Genome-Wide Association Studies
Whole Genome Assembly of Human Papillomavirus by Nanopore Long-Read Sequencing
Utilization of CRISPR-Mediated Tools for Studying Functional Genomics in Hematological Malignancies: An Overview on the Current Perspectives, Challenges, and Clinical Implications
We welcome Opinions, Perspectives, Hypotheses and Theory, and Mini-Review article types to facilitate this discussion. Please note, only relevant papers that add a significant contribution to the discussion articles will be considered.
This Research Topic aims to spark discussion around popular articles from 2022 in Genomic Assay Technology. This field is continuously evolving; therefore, we are seeking to understand developments and perspectives on articles that have attracted attention throughout the year.
The chosen manuscripts are:
Full-Length Spatial Transcriptomics Reveals the Unexplored Isoform Diversity of the Myocardium Post-MI
Combinatorial and Machine Learning Approaches for Improved Somatic Variant Calling from Formalin-Fixed Paraffin-Embedded Genome Sequence Data
Cell-Based NIPT Detects 47,XXY Genotype in a Twin Pregnancy
Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to Genotyping Arrays in Genome-Wide Association Studies
Whole Genome Assembly of Human Papillomavirus by Nanopore Long-Read Sequencing
Utilization of CRISPR-Mediated Tools for Studying Functional Genomics in Hematological Malignancies: An Overview on the Current Perspectives, Challenges, and Clinical Implications
We welcome Opinions, Perspectives, Hypotheses and Theory, and Mini-Review article types to facilitate this discussion. Please note, only relevant papers that add a significant contribution to the discussion articles will be considered.
Keywords: high-throughput screening platforms, robotic assay technologies, imaging, cytometry, analytical instrumentation and methods, Next-Gen sequencing, gene and genome characterization
Important Note: All contributions to this Research Topic must be within the scope of the section and journal to which they are submitted, as defined in their mission statements. Frontiers reserves the right to guide an out-of-scope manuscript to a more suitable section or journal at any stage of peer review.
