Evidence map›Paper›PMID 26567534›Full record

ArticleNature communications2015

Scalable amplification of strand subsets from chip-synthesized oligonucleotide libraries.

Thorsten L Schmidt, Brian J Beliveau, Yavuz O Uca, Mark Theilmann, Felipe Da Cruz, Chao-Ting Wu, William M Shih

Abstract read
In one paragraph

Article in Nature communications, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing 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

41 citing papers in PubMed.

  1. Article
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  7. Folding molecular origami from ribosomal RNA.Journal of nanobiotechnology · 2024
    Article
  8. Review
  9. Single-Cell Imaging of mRNA by Target RNA-Initiated RCA.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
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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

7 authors.

Thorsten L SchmidtDepartment of Cancer Biology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, Massachusetts 02215, USA.
Brian J BeliveauDepartment of Genetics, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, Massachusetts 02115, USA.
Yavuz O UcaCenter for Advancing Electronics Dresden (cfaed), Technische Universität Dresden, 01062, Dresden, Germany.
Mark TheilmannDepartment of Cancer Biology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, Massachusetts 02215, USA.
Felipe Da CruzWyss Institute for Biologically Inspired Engineering at Harvard, 3 Blackfan Circle, Boston, Massachusetts 02115, USA.
Chao-Ting WuDepartment of Genetics, Harvard Medical School, 77 Avenue Louis Pasteur, Boston, Massachusetts 02115, USA.
William M ShihDepartment of Cancer Biology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, Massachusetts 02215, USA.

Funding

The inheritance of position: It's not just who you are, it's where you areDP1GM106412 · NIGMS · HARVARD MEDICAL SCHOOL · PI WU, CHAO-TING · 2012 to 2016
$4.2M
NMR Structure Determination of Membrane Proteins Enabled by DNA NanotubesDP2OD004641 · OD · DANA-FARBER CANCER INST · PI SHIH, WILLIAM M · 2008 to 2008
$2.6M
A STUDY OF TRANSVECTION AT THE DROSOPHILA YELLOW GENER01GM061936 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI WU, CHAO-TING · 2000 to 2003
$1.7M
NCCDPHP CDC HHS 5DP1GM106412NIGMS NIH HHS DP1 GM106412NIGMS NIH HHS R01 GM061936NIGMS NIH HHS R01GM61936NIH HHS 1DP2OD004641NIH HHS DP2 OD004641
6 · The paper itself

Abstract

Synthetic oligonucleotides are the main cost factor for studies in DNA nanotechnology, genetics and synthetic biology, which all require thousands of these at high quality. Inexpensive chip-synthesized oligonucleotide libraries can contain hundreds of thousands of distinct sequences, however only at sub-femtomole quantities per strand. Here we present a selective oligonucleotide amplification method, based on three rounds of rolling-circle amplification, that produces nanomole amounts of single-stranded oligonucleotides per millilitre reaction. In a multistep one-pot procedure, subsets of hundreds or thousands of single-stranded DNAs with different lengths can selectively be amplified and purified together. These oligonucleotides are used to fold several DNA nanostructures and as primary fluorescence in situ hybridization probes. The amplification cost is lower than other reported methods (typically around US$ 20 per nanomole total oligonucleotides produced) and is dominated by the use of commercial enzymes.

Indexed as

DNA, Single-StrandedGene LibraryOligonucleotidesChromatography, High Pressure LiquidIn Situ Hybridization, FluorescenceNanostructuresNanotechnologyNucleic Acid Amplification TechniquesOligonucleotide Array Sequence AnalysisSynthetic BiologyDNA, Single-StrandedOligonucleotides

Identifiers

PMID26567534
PMCPMC4660042

What OpenQuestion holds

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LicenceCC BY
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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.