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Author Details
Full Name
Nathan D Olson
Affiliation
National Institute of Standards and Technology
ORCID
Career Start Year
2010
Papers
31
H Index
18
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37178559
Rapid production and free distribution of a synthetic RNA material to support SARS-CoV-2 molecular diagnostic testing.
Biologicals
2023
37961319
Benchmarking of small and large variants across tandem repeats.
bioRxiv
2023
37612512
The complete sequence of a human Y chromosome.
Nature
2023
37059810
Variant calling and benchmarking in an era of complete human genome sequences.
Nat Rev Genet
2023
36989327
Precision engineering of biological function with large-scale measurements and machine learning.
PLoS One
2023
35132260
Curated variation benchmarks for challenging medically relevant autosomal genes.
Nat Biotechnol
2022
35720974
PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions.
Cell Genom
2022
35357935
A complete reference genome improves analysis of human genetic variation.
Science
2022
34913592
The genotype-phenotype landscape of an allosteric protein.
Mol Syst Biol
2021
33784029
The genotype-phenotype landscape of an allosteric protein.
Mol Syst Biol
2021
32487205
Assembly and annotation of an Ashkenazi human reference genome.
Genome Biol
2020
32699374
Author Correction: A robust benchmark for detection of germline large deletions and insertions.
Nat Biotechnol
2020
32541955
A robust benchmark for detection of germline large deletions and insertions.
Nat Biotechnol
2020
28968737
Metagenomic assembly through the lens of validation: recent advances in assessing and improving the quality of genomes assembled from metagenomes.
Brief Bioinform
2019
31406327
Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome.
Nat Biotechnol
2019
31201313
High-coverage, long-read sequencing of Han Chinese trio reference samples.
Sci Data
2019
30936564
An open resource for accurately benchmarking small variant and reference calls.
Nat Biotechnol
2019
30821316
metagenomeFeatures: an R package for working with 16S rRNA reference databases and marker-gene survey feature data.
Bioinformatics
2019
30396371
Current progress and future opportunities in applications of bioinformatics for biodefense and pathogen detection: report from the Winter Mid-Atlantic Microbiome Meet-up, College Park, MD, January 10, 2018.
Microbiome
2018
29929281
Conventional wastewater treatment and reuse site practices modify bacterial community structure but do not eliminate some opportunistic pathogens in reclaimed water.
Sci Total Environ
2018
28063650
Performing Skin Microbiome Research: A Method to the Madness.
J Invest Dermatol
2017
28924496
Challenging a bioinformatic tool's ability to detect microbial contaminants using <i>in silico</i> whole genome sequencing data.
PeerJ
2017
28635638
Antibiotic Concentrations Decrease during Wastewater Treatment but Persist at Low Levels in Reclaimed Water.
Int J Environ Res Public Health
2017
27077050
Evaluation of microbial qPCR workflows using engineered Saccharomyces cerevisiae.
Biomol Detect Quantif
2016
26935931
PEPR: pipelines for evaluating prokaryotic references.
Anal Bioanal Chem
2016
26217378
Best practices for evaluating single nucleotide variant calling methods for microbial genomics.
Front Genet
2015
27077030
International interlaboratory study comparing single organism 16S rRNA gene sequencing data: Beyond consensus sequence comparisons.
Biomol Detect Quantif
2015
24217873
Diazotrophic diversity in the Caribbean coral, Montastraea cavernosa.
Arch Microbiol
2013
22706055
Impact of processing method on recovery of bacteria from wipes used in biological surface sampling.
Appl Environ Microbiol
2012
23206278
DNA extract characterization process for microbial detection methods development and validation.
BMC Res Notes
2012
20674366
Nitrogen fixation and nitrogen transformations in marine symbioses.
Trends Microbiol
2010
1 - 31 of 31
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