Cited by 659Genomics and Phylogenetic StudiesSingle-cell and spatial transcriptomicsGene expression and cancer classification

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Synthetic spike-in standards for RNA-seq experiments

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Jiang, Lichun, Schlesinger, Felix, Davis, Carrie A., Zhang, Yu, Li, Renhua, Salit, Marc, Gingeras, Thomas R., Oliver, Brian·2011·Genome Research

DOI 10.1101/gr.121095.111PMC PMC3166838

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Abstract

High-throughput sequencing of cDNA (RNA-seq) is a widely deployed transcriptome profiling and annotation technique, but questions about the performance of different protocols and platforms remain. We used a newly developed pool of 96 synthetic RNAs with various lengths, and GC content covering a 2 20 concentration range as spike-in controls to measure sensitivity, accuracy, and biases in RNA-seq experiments as well as to derive standard curves for quantifying the abundance of transcripts. We observed linearity between read density and RNA input over the entire detection range and excellent agreement between replicates, but we observed significantly larger imprecision than expected under pure Poisson sampling errors. We use the control RNAs to directly measure reproducible protocol-dependent biases due to GC content and transcript length as well as stereotypic heterogeneity in coverage across transcripts correlated with position relative to RNA termini and priming sequence bias. These effects lead to biased quantification for short transcripts and individual exons, which is a serious problem for measurements of isoform abundances, but that can partially be corrected using appropriate models of bias. By using the control RNAs, we derive limits for the discovery and detection of rare transcripts in RNA-seq experiments. By using data collected as part of the model organism and human Encyclopedia of DNA Elements projects (ENCODE and modENCODE), we demonstrate that external RNA controls are a useful resource for evaluating sensitivity and accuracy of RNA-seq experiments for transcriptome discovery and quantification. These quality metrics facilitate comparable analysis across different samples, protocols, and platforms.

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Authors: Jiang, L., Schlesinger, F., Davis, C. A., Zhang, Y., Li, R., Salit, M., Gingeras, T. R., & Oliver, B.
Affiliations: National Institutes of Health (US)
Cold Spring Harbor Laboratory (US)
National Institute of Standards and Technology (US)
ORCID: Jiang, Lichun
Zhang, Yu
Salit, Marc
Gingeras, Thomas R.
Oliver, Brian
Venue: Genome Research
Publisher: Cold Spring Harbor Laboratory
Published: 2011-08-04
Volume: 21
Issue: 9
Pages: 1543-1551
ISSN: 1088-9051 (ISSN-L)
DOI: 10.1101/gr.121095.111
PMC: PMC3166838
OpenAlex: W2009458183
Cited by: 653
References: 44
Citations by year: 2026: 18 · 2025: 35 · 2024: 50 · 2023: 36 · 2022: 53 · 2021: 45 · 2020: 58 · 2019: 54 · 2018: 51 · 2017: 67 · 2016: 64 · 2015: 38 · 2014: 40 · 2013: 25 · 2012: 15
Type: posted content
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Locations: Genome Research (publishedVersion)
Europe PMC (PubMed Central) (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Cold Spring Harbor Laboratory Institutional Repository (Cold Spring Harbor Laboratory) (acceptedVersion)
HighWire Press Open Archive (submittedVersion)
Funders: National Institutes of Health
National Institute of Standards and Technology
National Human Genome Research Institute (U54HG004557)
National Institute of Diabetes and Digestive and Kidney Diseases (ZIADK015600)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Phylogenetic Studies
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Single-cell and spatial transcriptomics
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene expression and cancer classification
Keywords: RNA-seq, transcriptome quantification, GC content bias, calibration curve, isoform abundance, ENCODE, modENCODE
MeSH terms: Animals, Humans, Quality Control, RNA, Sensitivity and Specificity, Reproducibility of Results, Gene Library, Bias, Sequence Analysis, RNA, Gene Expression Profiling, High-Throughput Nucleotide Sequencing

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