Evidence map›Paper›PMID 42681046›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

Isolation of RNA for RNA Sequencing in Ustilago maydis.

Amanda M Seto, Barry J Saville

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. 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

2 authors.

Amanda M SetoEnvironmental and Life Sciences Graduate Program, Trent University, Peterborough, ON, Canada.
Barry J SavilleDepartment of Forensic Science, Trent University, Peterborough, ON, Canada. barrysaville@trentu.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In the last 15 years, RNA sequencing (RNA-seq) has emerged as a popular tool for studying gene expression changes in an organism. In fungal plant pathology, this is a comprehensive method for identifying transcriptome changes to both the fungal pathogen and its host. RNA-seq generates a vast amount of data that can increase our understanding of the interaction between the fungus and its host, or how the fungal species adapts to various environmental conditions. This chapter emphasizes the importance of sample preparation for RNA-seq. It also describes a protocol for isolating high quality RNA from Ustilago maydis haploid, dikaryon, and teliospore samples, removing genomic DNA contamination and screening RNA to ensure its removal, and it provides a method for cDNA library preparation. Successful RNA-seq experiments require careful handling of RNA during isolation and its downstream steps. Careful handling enables RNA sequencing to generate vast amounts of information on transcriptome changes, which can provide meaningful insights into the growth and development of U. maydis.

Indexed as

RNA, FungalSequence Analysis, RNAUstilagoBasidiomycotaGene Expression ProfilingGene LibraryHigh-Throughput Nucleotide SequencingTranscriptomeRNA, FungalcDNA library creationPrecautions in RNA isolationRNA-seqTotal RNA isolationUstilago maydis

Identifiers

PMID42681046

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.