Low-Pass Whole Genome Sequencing

Low-Pass Whole Genome Sequencing (LP-WGS or low-coverage whole-genome sequencing) is an inexpensive high-throughput technology for detecting genome-wide genetic variation in a multitude of species.

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Genotyping by low-coverage whole-genome sequencing in intercross

Abstract 11316: Analytical Validation for an Integrated Risk Tool

Ultra-low-pass whole-genome sequencing of circulating tumor DNA

A team from the Chinese University of Hong Kong Medical School

Complete Genomics and Gencove Partner for Bundled Low-Pass Whole

Copy number profiling using nanopore low-pass whole genome

Clinical utilisation of a rapid low-pass whole genome sequencing

Best practices for analyzing imputed genotypes from low-pass

Enhancing Prenatal Screening with Low-Pass Genome Sequencing

Low-pass whole-genome sequencing in clinical cytogenetics: a

The $100 Genome Azenta Life Sciences

Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores, Genome Medicine

Low-coverage single-cell mRNA sequencing reveals cellular heterogeneity and activated signaling pathways in developing cerebral cortex

The Coverage Gap: Uninsured Poor Adults in States that Do Not Expand Medicaid – An Update - Issue Brief - 8659-03

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Evaluating coverage bias in next-generation sequencing of