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List of works by Justin M Zook

A Rigorous Interlaboratory Examination of the Need to Confirm NGS-Detected Variants by an Orthogonal Method in Clinical Genetic Testing

A Rigorous Interlaboratory Examination of the Need to Confirm Next-Generation Sequencing-Detected Variants with an Orthogonal Method in Clinical Genetic Testing

scientific article published on 03 January 2019

A diploid assembly-based benchmark for variants in the major histocompatibility complex

scientific article published on 22 September 2020

A draft human pangenome reference

scientific article published on 10 May 2023

A research roadmap for next-generation sequencing informatics

scientific article published on April 2016

A robust benchmark for detection of germline large deletions and insertions

scientific article published on 15 June 2020

Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome

scientific article published on 12 August 2019

Achieving high-sensitivity for clinical applications using augmented exome sequencing

scientific article

Advancing Benchmarks for Genome Sequencing

scientific article published on 23 September 2015

An open resource for accurately benchmarking small variant and reference calls

scientific article published on 01 April 2019

Assuring the quality of next-generation sequencing in clinical laboratory practice

scientific article

Author Correction: A robust benchmark for detection of germline large deletions and insertions

scientific article published on 22 July 2020

Author Correction: Best practices for benchmarking germline small-variant calls in human genomes

scientific article published on 01 May 2019

Best practices for benchmarking germline small-variant calls in human genomes

scientific article published on 11 March 2019

Challenging a bioinformatic tool's ability to detect microbial contaminants using in silico whole genome sequencing data.

scientific article published on 12 September 2017

Chromosome-scale, haplotype-resolved assembly of human genomes

scientific article published on 07 December 2020

Curated variation benchmarks for challenging medically relevant autosomal genes

scientific article published in 2022

Current-polarized ion-selective membranes: The influence of plasticizer and lipophilic background electrolyte on concentration profiles, resistance, and voltage transients.

scientific article published on March 2009

Integrating human sequence data sets provides a resource of benchmark SNP and indel genotype calls

scientific article

Interpretation of chronopotentiometric transients of ion-selective membranes with two transition times.

scientific article published on January 2010

Magnetic connectors for microfluidic applications

scientific article published on 16 November 2009

Measuring agglomerate size distribution and dependence of localized surface plasmon resonance absorbance on gold nanoparticle agglomerate size using analytical ultracentrifugation.

scientific article published on 29 September 2011

Measuring silver nanoparticle dissolution in complex biological and environmental matrices using UV–visible absorbance

scientific article published on 02 August 2011

Medical implications of technical accuracy in genome sequencing

scientific article

Nanopore sequencing and the Shasta toolkit enable efficient de novo assembly of eleven human genomes

scientific article published on 04 May 2020

Performance assessment of DNA sequencing platforms in the ABRF Next-Generation Sequencing Study

scientific article published on 09 September 2021

Stable nanoparticle aggregates/agglomerates of different sizes and the effect of their size on hemolytic cytotoxicity.

scientific article

Synthetic spike-in standards improve run-specific systematic error analysis for DNA and RNA sequencing

scientific article

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