Evidence map›Paper›PMID 36697673›Full record

ArticleCommunications chemistry2022

Advanced preparation of fragment libraries enabled by oligonucleotide-modified 2',3'-dideoxynucleotides.

Justina Medžiūnė, Žana Kapustina, Simona Žeimytė, Jevgenija Jakubovska, Rūta Sindikevičienė, Inga Čikotienė, Arvydas Lubys

Abstract read
In one paragraph

Article in Communications chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. A comprehensive review onFrontiers in genetics · 2024
    Review
  3. Article
  4. Article
  5. Review
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.

Justina Medžiūnė *Department of Research and Development, Thermo Fisher Scientific Baltics, Vilnius, LT-02241, Lithuania. justina.medziune@thermofisher.com.ORCID http://orcid.org/0000-0003-0474-5184
Žana Kapustina *Department of Research and Development, Thermo Fisher Scientific Baltics, Vilnius, LT-02241, Lithuania.
Simona ŽeimytėDepartment of Research and Development, Thermo Fisher Scientific Baltics, Vilnius, LT-02241, Lithuania.
Jevgenija JakubovskaDepartment of Research and Development, Thermo Fisher Scientific Baltics, Vilnius, LT-02241, Lithuania.
Rūta SindikevičienėDepartment of Research and Development, Thermo Fisher Scientific Baltics, Vilnius, LT-02241, Lithuania.
Inga ČikotienėDepartment of Research and Development, Thermo Fisher Scientific Baltics, Vilnius, LT-02241, Lithuania.
Arvydas LubysDepartment of Research and Development, Thermo Fisher Scientific Baltics, Vilnius, LT-02241, Lithuania.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ever-growing demand for inexpensive, rapid, and accurate exploration of genomes calls for refinement of existing sequencing techniques. The development of next-generation sequencing (NGS) was a revolutionary milestone in genome analysis. While modified nucleotides already were inherent tools in sequencing and imaging, further modification of nucleotides enabled the expansion into even more diverse applications. Herein we describe the design and synthesis of oligonucleotide-tethered 2',3'-dideoxynucleotide (dd

Identifiers

PMID36697673
PMCPMC9814608

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.