Evidence map›Paper›PMID 41318777›Full record

ArticleScientific reports2025

Fabrication of microcolumn arrays for high-throughput oligonucleotide synthesis using 3D printing.

Haeun Kim, Junhyeong Kim, Duhee Bang

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Haeun Kim *Department of Chemistry, Yonsei University, Seoul, Korea.
Junhyeong Kim *Department of Chemistry, Yonsei University, Seoul, Korea.
Duhee BangDepartment of Chemistry, Yonsei University, Seoul, Korea. duheebang@yonsei.ac.kr.

Funding

korea government(MSIT) RS-2024-00338316Ministry of Science, ICT and Future Planning RS-2022-NR067569
6 · The paper itself

Abstract

Advances in high-density oligonucleotide array synthesis have enabled the creation of increasingly large DNA libraries. However, current planar array platforms are designed to synthesize only femtomole-scale amounts of oligonucleotides per feature, due to their inherently small feature sizes and high spatial density. Conversely, column-based synthesis supports higher per-feature output but accommodates fewer sequences. In this study, we introduce a 3D-printed DNA synthesis substrate that combines the strengths of both approaches. Using an LCD-based 3D printer and photopolymer resins, we fabricated micrometer-scale columns filled with controlled pore glass (CPG), enabling high-density oligonucleotide synthesis with sub-nanomole-scale output per feature. We screened commercial resins for chemical resistance and optimized printing parameters to fabricate rectangular microholes with gap widths smaller than CPG beads, capable of securely retaining CPG beads. A 15-mer poly(dT) sequence was synthesized across 1000 microcolumns on the array using an inkjet-based phosphoramidite system. The substrate was fabricated in ~ 2.5 h at an estimated material cost of just $0.12 per unit.

Identifiers

PMID41318777
PMCPMC12769683

What OpenQuestion holds

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Registered trials

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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.