Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an

Non-Invasive Detection of Breast Cancer by Low-Coverage Whole-Genome Sequencing from Plasma

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

Reconstruction of the personal information from human genome reads in gut metagenome sequencing data

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

Low-Pass Whole Genome Sequencing

Targeted genomic sequencing with probe capture for discovery and surveillance of coronaviruses in bats

Pan-genome - Wikipedia

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

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

Low-coverage whole genome sequencing for a highly selective cohort of severe COVID-19 patients

Low-Pass Whole Genome Sequencing

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

You Can Get Your Whole Genome Sequenced. But Should You?

Frontiers Comparison of Genotype Imputation for SNP Array and