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 and esteemed Associate Editors.
This Research Topic aims to spark discussion around some of the most developing areas in the Genomic Assay Technology field including spatial transcriptomic data, machine learning approaches, NIPT assays, Ultra Low/ Low-Coverage Whole-Genome Sequencing, or usage of Long- Read Sequencing like Nanopore sequencing or novel sequencing techniques. This field is continuously evolving; therefore, we are seeking to understand developments and perspectives on themes represented by the 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 Theories, Mini-Review articles or Original Research on themes such as:
Spatial Transcriptomic Data
Machine Learning approaches
NIPT assays
Ultra Low-Coverage Whole-Genome Sequencing
Nanopore Long-Read Sequencing
This Research Topic aims to spark discussion around some of the most developing areas in the Genomic Assay Technology field including spatial transcriptomic data, machine learning approaches, NIPT assays, Ultra Low/ Low-Coverage Whole-Genome Sequencing, or usage of Long- Read Sequencing like Nanopore sequencing or novel sequencing techniques. This field is continuously evolving; therefore, we are seeking to understand developments and perspectives on themes represented by the 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 Theories, Mini-Review articles or Original Research on themes such as:
Spatial Transcriptomic Data
Machine Learning approaches
NIPT assays
Ultra Low-Coverage Whole-Genome Sequencing
Nanopore Long-Read Sequencing
Keywords: Spatial Transcriptomic Data, Machine Learning approaches, NIPT assays, Ultra Low-Coverage Whole-Genome Sequencing, Nanopore Long-Read Sequencing
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.
