SPANDx workflow for analysis of haploid next-generation re-sequencing data.

SPANDx workflow for analysis of haploid next-generation re

Emergent biomarker derived from next-generation sequencing to

SPANDx workflow for analysis of haploid next-generation re

Whole-genome sequencing for neonatal intensive care unit outbreak

Opportunistic pathogens and large microbial diversity detected in

Whole-genome sequencing for neonatal intensive care unit outbreak

Analysis of the 9p21.3 sequence associated with coronary artery

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The Northern Arizona SNP Pipeline (NASP): accurate, flexible, and

Detection of repeat expansions in large next generation DNA and

Automation Enhances Next-Generation Sequencing Workflows

PDF) SPANDx: A genomics pipeline for comparative analysis of large haploid whole genome re-sequencing datasets

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