Enabling low-pass whole genome sequencing

Low-pass whole-genome sequencing is an effective technical alternative to microarray-based genotyping | seqWell makes that happen

Genetic data

Enabling low-pass whole genome sequencing

Three Ways Gencove's Low-Pass Whole Genome Sequencing is Modernizing the Drug Discovery Process - Gencove

A protocol for applying low-coverage whole-genome sequencing data in structural variation studies

A protocol for applying low-coverage whole-genome sequencing data in structural variation studies

In celebration of World Wildlife Day, we are highlighting the California Conservation Genomics Project and UC…

Low-Pass Genome Sequencing: Validation and Diagnostic Utility from 409 Clinical Cases of Low-Pass Genome Sequencing for the Detection of Copy Number Variants to Replace Constitutional Microarray - ScienceDirect

Whole-genome sequencing reveals progressive versus stable myeloma precursor conditions as two distinct entities

Pathogen Genomics in Public Health

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

Cell-free DNA ultra-low-pass whole genome sequencing to distinguish malignant peripheral nerve sheath tumor (MPNST) from its benign precursor lesion: A cross-sectional study

Genomics platform

Paired-End vs. Single-Read Sequencing Technology

Download Now - Low-pass Whole Genome Sequencing Application Note