Evidence map›Paper›PMID 30872414›Full record

ArticleRNA (New York, N.Y.)2019

Analysis of differential gene expression and alternative splicing is significantly influenced by choice of reference genome.

Erin Slabaugh, Jigar S Desai, Ryan C Sartor, Lovely Mae F Lawas, S V Krishna Jagadish, Colleen J Doherty

Abstract read
In one paragraph

Article in RNA (New York, N.Y.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

6 authors.

Erin Slabaugh *Department of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, North Carolina 27695, USA.
Jigar S Desai *Department of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, North Carolina 27695, USA.ORCID 0000-0002-5238-3619
Ryan C SartorCrop and Soil Science Department, North Carolina State University, Raleigh, North Carolina 27695, USA.ORCID 0000-0002-9621-0824
Lovely Mae F LawasInternational Rice Research Institute (IRRI), DAPO Box 7777, Metro Manila, Philippines.
S V Krishna JagadishInternational Rice Research Institute (IRRI), DAPO Box 7777, Metro Manila, Philippines.
Colleen J DohertyDepartment of Molecular and Structural Biochemistry, North Carolina State University, Raleigh, North Carolina 27695, USA.ORCID 0000-0003-1126-5592

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RNA-seq analysis has enabled the evaluation of transcriptional changes in many species including nonmodel organisms. However, in most species only a single reference genome is available and RNA-seq reads from highly divergent varieties are typically aligned to this reference. Here, we quantify the impacts of the choice of mapping genome in rice where three high-quality reference genomes are available. We aligned RNA-seq data from a popular productive rice variety to three different reference genomes and found that the identification of differentially expressed genes differed depending on which reference genome was used for mapping. Furthermore, the ability to detect differentially used transcript isoforms was profoundly affected by the choice of reference genome: Only 30% of the differentially used splicing features were detected when reads were mapped to the more commonly used, but more distantly related reference genome. This demonstrated that gene expression and splicing analysis varies considerably depending on the mapping reference genome, and that analysis of individuals that are distantly related to an available reference genome may be improved by acquisition of new genomic reference material. We observed that these differences in transcriptome analysis are, in part, due to the presence of single nucleotide polymorphisms between the sequenced individual and each respective reference genome, as well as annotation differences between the reference genomes that exist even between syntenic orthologs. We conclude that even between two closely related genomes of similar quality, using the reference genome that is most closely related to the species being sampled significantly improves transcriptome analysis.

Indexed as

Genes, EssentialGenome, PlantTranscriptomeAlternative SplicingBase SequenceChromosome MappingGene Expression ProfilingHigh-Throughput Nucleotide SequencingOryzaPolymorphism, Single NucleotideReference StandardsRNA, MessengerSequence AlignmentRNA, Messengerdifferential gene expressionOryza sativareference genomeRNA-seqsplicingtranscriptome analysis

Identifiers

PMID30872414
PMCPMC6521602

What OpenQuestion holds

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Read underepoch 390

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.