Enabling low-pass whole genome sequencing
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Low-pass whole-genome sequencing is an effective technical alternative to microarray-based genotyping | seqWell makes that happen
Low-Pass Whole-Genome Sequencing as a Method of Determining Copy Number Variations in Uveal Melanoma Tissue Samples - ScienceDirect
Diagnostics, Free Full-Text
A protocol for applying low-coverage whole-genome sequencing data in structural variation studies - ScienceDirect
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Single-cell genome sequencing: current state of the science
Enabling CNV Studies from Single Cells Using Whole Genome Amplification and Low Pass Sequencing
MGI - Genetic sequencing and multi-omics solutions for life science and healthcare research
New method improves accuracy of DNA sequencing 1000-fold to detect rare genetic mutations
Genome-wide mutational signatures in low-coverage whole genome sequencing of cell-free DNA
