Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an

Frontiers A Study Protocol for Validation and Implementation of Whole- Genome and -Transcriptome Sequencing as a Comprehensive Precision Diagnostic Test in Acute Leukemias

Frontiers Towards a Cost-Effective Implementation of Genomic Prediction Based on Low Coverage Whole Genome Sequencing in Dezhou Donkey

Low-Pass Whole Genome Sequencing

Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an Alternative to Genotyping Arrays in Genome-Wide Association Studies

Frontiers Advancing animal tuberculosis surveillance using culture-independent long-read whole-genome sequencing

Application of long-read sequencing to the detection of structural variants in human cancer genomes - Computational and Structural Biotechnology Journal

A complete telomere-to-telomere assembly of the maize genome

Bacterial single-cell whole genome sequencing

Frontiers A Rapid, Whole Genome Sequencing Assay for Detection and Characterization of Novel Coronavirus (SARS-CoV-2) Clinical Specimens Using Nanopore Sequencing

Frontiers Feasibility to use whole-genome sequencing as a sole diagnostic method to detect genomic aberrations in pediatric B-cell acute lymphoblastic leukemia

Ultra-low coverage fragmentomic model of cell-free DNA for cancer detection based on whole-exome regions

Low-coverage whole-genome sequencing of extracellular vesicle-associated DNA in patients with metastatic cancer

PDF] Low-pass Whole-genome Sequencing of Circulating Cell-free DNA Demonstrates Dynamic Changes in Genomic Copy Number in a Squamous Lung Cancer Clinical Cohort