Frontiers Ultra Low-Coverage Whole-Genome Sequencing as an

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Frontiers Low-Coverage Whole Genome Sequencing of Cell-Free DNA From Immunosuppressed Cancer Patients Enables Tumor Fraction Determination and Reveals Relevant Copy Number Alterations

Phasing analysis of lung cancer genomes using a long read sequencer

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

Frontiers SARS-CoV-2 Whole-Genome Sequencing Using Oxford Nanopore Technology for Variant Monitoring in Wastewaters

Frontiers Whole-genome/exome analysis of circulating tumor DNA

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

Combining targeted sequencing and ultra-low-pass whole-genome sequencing for accurate somatic copy number alteration detection

Bacterial single-cell whole genome sequencing

Genes, Free Full-Text

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

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