Frontiers Methods to improve the accuracy of next-generation sequencing
Low-coverage whole genome sequencing for a highly selective cohort of severe COVID-19 patients
Copy number profiling using nanopore low-pass whole genome
Bacterial single-cell whole genome sequencing
Frontiers Low-Coverage Whole Genome Sequencing of Cell-Free DNA From Immunosuppressed Cancer Patients Enables Tumor Fraction Determination and Reveals Relevant Copy Number Alterations
Long walk to genomics: History and current approaches to genome sequencing and assembly - ScienceDirect
Low-coverage whole-genome sequencing of extracellular vesicle-associated DNA in patients with metastatic cancer
Frontiers Long-Read Sequencing Emerging in Medical Genetics
Frontiers A Rapid, Whole Genome Sequencing Assay for Detection and Characterization of Novel Coronavirus (SARS-CoV-2) Clinical Specimens Using Nanopore Sequencing
Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to Genotyping Arrays in Genome-Wide Association Studies
Single duplex DNA sequencing with CODEC detects mutations with high sensitivity
Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to Genotyping Arrays in Genome-Wide Association Studies
Frontiers Whole Genome Sequencing of Influenza A and B Viruses With the MinION Sequencer in the Clinical Setting: A Pilot Study
Frontiers Application of third-generation sequencing to herbal genomics