Evidence map›Paper›PMID 36768872›Full record

ArticleInternational journal of molecular sciences2023

Scalable Combinatorial Assembly of Synthetic DNA for Tracking Applications.

Julius D Stuart, Natalie R Wickenkamp, Kaleb A Davis, Camden Meyer, Rebekah C Kading, Christopher D Snow

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Julius D StuartDepartment of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.ORCID 0000-0003-0214-4481
Natalie R WickenkampDepartment of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, CO 80523, USA.
Kaleb A DavisDepartment of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, CO 80523, USA.
Camden MeyerDepartment of Chemical and Biological Engineering, Colorado State University, Fort Collins, CO 80523, USA.
Rebekah C KadingDepartment of Microbiology, Immunology, and Pathology, Colorado State University, Fort Collins, CO 80523, USA.ORCID 0000-0002-4996-915X
Christopher D SnowDepartment of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.ORCID 0000-0002-7690-3519

Funding

NIH Prior Approval Process ProfessionalUL1TR002535 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2018 to 2022
$51.1M
CSU Infectious Disease Research and Response Training ProgramT32AI162691 · NIAID · COLORADO STATE UNIVERSITY · PI DEAN, GREGG A · 2021 to 2025
$2.1M
Surveillance of mosquito and arbovirus dispersal using smart microcrystalsR21AI146740 · NIAID · COLORADO STATE UNIVERSITY · PI KADING, REBEKAH CROCKETT · 2019 to 2020
$405k
NCATS NIH HHS UL1 TR002535NIAID NIH HHS R21 AI146740NIAID NIH HHS T32 AI162691NIH HHS AI146740
6 · The paper itself

Abstract

Synthetic DNA barcodes are double-stranded DNA molecules designed to carry recoverable information, information that can be used to represent and track objects and organisms. DNA barcodes offer robust, sensitive detection using standard amplification and sequencing techniques. While numerous research groups have promoted DNA as an information storage medium, less attention has been devoted to the design of economical, scalable DNA barcode libraries. Here, we present an alternative modular approach to sequence design. Barcode sequences were constructed from smaller, interchangeable blocks, allowing for the combinatorial assembly of numerous distinct tags. We demonstrated the design and construction of first-generation (N = 256) and second-generation (N = 512) modular barcode libraries, from fewer than 50 total single-stranded oligonucleotides for each library. To avoid contamination during experimental validation, a liquid-handling robot was employed for oligonucleotide mixing. Generating barcode sequences in-house reduces dependency upon external entities for unique tag generation, increasing flexibility in barcode generation and deployment. Next generation sequencing (NGS) detection of 256 different samples in parallel highlights the multiplexing afforded by the modular barcode design coupled with high-throughput sequencing. Deletion variant analysis of the first-generation library informed sequence design for enhancing barcode assembly specificity in the second-generation library.

Indexed as

DNADNA Barcoding, TaxonomicGene LibraryHigh-Throughput Nucleotide SequencingOligonucleotidesSequence Analysis, DNADNAOligonucleotidescombinatorial librarycomputational designDNA assemblynext-generation sequencingsurveillancesynthetic DNA barcodingsynthetic DNA tags

Identifiers

PMID36768872
PMCPMC9917336

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.