Evidence map›Paper›PMID 32968351›Full record

ArticleBreeding science2020

Low-cost RNA extraction method for highly scalable transcriptome studies.

Kanami Yoshino, Ryo Nishijima, Taiji Kawakatsu

Abstract read
In one paragraph

Article in Breeding science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Total RNA Extraction from Rice Vegetative Tissues Using Magnetic Beads.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. 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.

Kanami YoshinoInstitute of Agrobiological Sciences, National Agriculture and Food Research Organization, 3-1-3 Kan-nondai, Tsukuba, Ibaraki 305-8604, Japan.
Ryo NishijimaInstitute of Agrobiological Sciences, National Agriculture and Food Research Organization, 3-1-3 Kan-nondai, Tsukuba, Ibaraki 305-8604, Japan.
Taiji KawakatsuInstitute of Agrobiological Sciences, National Agriculture and Food Research Organization, 3-1-3 Kan-nondai, Tsukuba, Ibaraki 305-8604, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA extraction has been improved by integration of a variety of materials in the protocol, such as phenol, guanidine thiocyanate, and silica, according to the case-specific demands. However, few methods have been designed for high-throughput RNA preparation for large-scale transcriptome studies. In this study, we established a high-throughput guanidinium thiocyanate and isopropyl alcohol based RNA extraction method (HighGI). HighGI is based on simple and phenol-free homemade buffers and the cost is substantially lower than a column-based commercial kit. We demonstrated that the quality and quantity of RNA extracted with HighGI were comparable to those extracted with a conventional phenol/chloroform-based method and a column-based commercial kit. HighGI retained small RNAs less than 200 bp, which are lost with a commercial column-based kit. We also demonstrated that HighGI is readily applicable to semi-automated RNA extraction. HighGI enables high-throughput RNA extraction for large-scale RNA preparation with high yield and quality.

Indexed as

guanidinium thiocyanatehigh-throughput RNA extractionmagnetic beadssmall RNA extraction

Identifiers

PMID32968351
PMCPMC7495201

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.