Evidence map›Paper›PMID 38849559›Full record

ArticleNature computational science2024

Scalable design of orthogonal DNA barcode libraries.

Gokul Gowri, Kuanwei Sheng, Peng Yin

Abstract read
In one paragraph

Article in Nature computational science, 2024. 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

3 authors.

Gokul GowriDepartment of Systems Biology, Harvard Medical School, Boston, MA, USA. ggowri@g.harvard.edu.ORCID 0000-0003-0911-6889
Kuanwei ShengDepartment of Systems Biology, Harvard Medical School, Boston, MA, USA.ORCID 0000-0002-7155-9915
Peng YinDepartment of Systems Biology, Harvard Medical School, Boston, MA, USA. py@hms.harvard.edu.ORCID 0000-0002-4773-359X

Funding

High-throughput single-molecule protein identification via super-resolution imagingDP1GM133052 · NIGMS · HARVARD UNIVERSITY · PI YIN, PENG · 2018 to 2022
$6.6M
Platform technologies for scalable highly multiplexed proteomic phenotyping of the brainRF1MH128861 · NIMH · HARVARD UNIVERSITY · PI CHUNG, KWANGHUN, DONG, HONG-WEI · 2021 to 2021
$5.5M
Decoding chromosome structure with multiplexed super-resolution microscopyR01GM124401 · NIGMS · HARVARD UNIVERSITY · PI YIN, PENG · 2018 to 2021
$2.5M
Light-Seq: Spatially targeted profiling of transcriptomic states in cells and tissueR01HG012926 · NHGRI · HARVARD UNIVERSITY · PI Peng Yin · 2023 to 2026
$2.3M
NHGRI NIH HHS R01 HG012926NIGMS NIH HHS DP1 GM133052NIGMS NIH HHS R01 GM124401NIMH NIH HHS RF1 MH128861U.S. Department of Health & Human Services | National Institutes of Health (NIH) DP1GM133052U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01GM124401U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01HG012926U.S. Department of Health & Human Services | National Institutes of Health (NIH) RF1MH128861
6 · The paper itself

Abstract

Orthogonal DNA barcode library design is an essential task in bioengineering. Here we present seqwalk, an efficient method for designing barcode libraries that satisfy a sequence symmetry minimization (SSM) heuristic for orthogonality, with theoretical guarantees of maximal or near-maximal library size under certain design constraints. Seqwalk encodes SSM constraints in a de Bruijn graph representation of sequence space, enabling the application of recent advances in discrete mathematics

Indexed as

DNA Barcoding, TaxonomicGene LibraryAlgorithmsDNADNA

Identifiers

PMID38849559
PMCPMC11208133

What OpenQuestion holds

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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.