The DOI matches its Crossref record; 43 of the 44 references it cites were found in a registry or an index.
RNA-Seq: a revolutionary tool for transcriptomics
Open accessAbstract
RNA-Seq is a recently developed approach to transcriptome profiling that uses deep-sequencing technologies. Studies using this method have already altered our view of the extent and complexity of eukaryotic transcriptomes. RNA-Seq also provides a far more precise measurement of levels of transcripts and their isoforms than other methods. This article describes the RNA-Seq approach, the challenges associated with its application, and the advances made so far in characterizing several eukaryote transcriptomes.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“High-throughput transcriptome sequencing and digital gene expression (DGE) tag profiling are efficient and economic choice for characterizing non-model organisms without a reference genome [9], [10].”
From Digital Gene Expression Analysis Based on Integrated De Novo Transcriptome Assembly of Sweet Potato [Ipomoea batatas (L.) Lam.] (2012) · cites this paper as [10]
Experimental — accuracy not yet measuredIn the citing paper
“RNA-Seq provides comprehensive information on mRNA abundance, alternative splicing, nucleotide variation, and structure alteration.”
From Integrative Analysis of Multi-omics Data for Discovery and Functional Studies of Complex Human Diseases (2016) · cites this paper as Z. Wang et al., 2009
In the citing paper
“mNGS of RNA libraries used for the detection of pathogens such as RNA viruses in clinical samples incidentally produces host gene expression data for transcriptome (RNA-seq) analyses66.”
From Clinical metagenomics (2019) · cites this paper as [66]
In the citing paper
“Most studies have been conducted on small sample sizes and not tested on independent cohorts, or used older microarray technology, which is less accurate and reproducible than modern RNA sequencing85,86.”
From Measuring biological age using omics data (2022) · cites this paper as [85]
In the citing paper
“It should be emphasized that development of new experimental techniques such as deep-sequencing RNA-Seq,90 provides new types of data for in vitro assessment of toxicities that can also be used for QSAR modeling.91”
From QSAR without borders (2020) · cites this paper as [90]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Mapping and quantifying mammalian transcriptomes by RNA-Seq
Mortazavi, A., Williams, B. A., McCue, K., Schaeffer, L., & Wold, B. (2008) · Nature Methods · doi:10.1038/nmeth.1226 · Cited by 13,696
Serial Analysis of Gene Expression
Velculescu, V. E., Zhang, L., Vogelstein, B., & Kinzler, K. W. (1995) · Science · doi:10.1126/science.270.5235.484 · Cited by 3,713
SOAP: Short oligonucleotide alignment program
Li, R., Li, Y., Kristiansen, K., & Wang, J. (2008) · Bioinformatics · doi:10.1093/bioinformatics/btn025 · Cited by 3,597
RNA-seq: An assessment of technical reproducibility and comparison with gene expression arrays
Marioni, J. C., Mason, C. E., Mane, S. M., Stephens, M., & Gilad, Y. (2008) · Genome Research · doi:10.1101/gr.079558.108 · Cited by 2,771
Mapping short DNA sequencing reads and calling variants using mapping quality scores
Li, H., Ruan, J., & Durbin, R. (2008) · Genome Research · doi:10.1101/gr.078212.108 · Cited by 2,638
The Transcriptional Landscape of the Yeast Genome Defined by RNA Sequencing
Nagalakshmi, U., Wang, Z., Waern, K., Shou, C., Raha, D., Gerstein, M., & Snyder, M. (2008) · Science · doi:10.1126/science.1158441 · Cited by 2,479
Self-citationHighly Integrated Single-Base Resolution Maps of the Epigenome in Arabidopsis
Lister, R., O’Malley, R. C., Tonti‐Filippini, J., Gregory, B. D., Berry, C. C., Millar, A. H., & Ecker, J. R. (2008) · Cell · doi:10.1016/j.cell.2008.03.029 · Cited by 2,424
Gene expression analysis by massively parallel signature sequencing (MPSS) on microbead arrays.
Brenner, S., Johnson, M., Bridgham, J., Golda, G., Lloyd, D. H., Johnson, D., Luo, S., McCurdy, S., Foy, M., Ewan, M., et al. (2000) · Nature Biotechnology · doi:10.1038/76469 · Cited by 1,360
TRANSLATIONAL REGULATION OFGCN4AND THE GENERAL AMINO ACID CONTROL OF YEAST
Hinnebusch, A. G. (2005) · Annual Review of Microbiology · doi:10.1146/annurev.micro.59.031805.133833 · Cited by 1,297
Sultan, M., Schulz, M. H., Richard, H., Magen, A., Klingenhoff, A., Scherf, M., Seifert, M., Borodina, T., Soldatov, A., Parkhomchuk, D., et al. (2008) · Science · doi:10.1126/science.1160342 · Cited by 1,293
Flagged first, then by citations
1 of the 44 references couldn’t be matched to a known paper.
Cited by
Sorted by citations
Items 201–300 of 1,061
New insights into the blood‐stage transcriptome of Plasmodium falciparum using RNA‐Seq
Otto, T. D., Wilinski, D., Assefa, S. A., Keane, T., Sarry, L. R., Böhme, U., Lemieux, J. E., Barrell, B. G., Pain, A., Berriman, M., et al. (2010) · Molecular Microbiology · doi:10.1111/j.1365-2958.2009.07026.x · Cited by 394
Recurrent SETBP1 mutations in atypical chronic myeloid leukemia
Piazza, R., Valletta, S., Winkelmann, N., Redaelli, S., Spinelli, R., Pirola, A., Antolini, L., Mologni, L., Donadoni, C., Papaemmanuil, E., et al. (2012) · Nature Genetics · doi:10.1038/ng.2495 · Cited by 400
A multidimensional systems biology analysis of cellular senescence in aging and disease
Avelar, R. A., Ortega, J. G., Tacutu, R., Tyler, E. J., Bennett, D., Binetti, P., Budovsky, A., Chatsirisupachai, K., Johnson, E., Murray, A., et al. (2020) · Genome Biology · doi:10.1186/s13059-020-01990-9 · Cited by 399
Shi, C.-Y., Yang, H., Wei, C., Yu, O. S., Zhang, Z., Jiang, C., Sun, J., Li, Y., Chen, Q., Xia, T., et al. (2011) · BMC Genomics · doi:10.1186/1471-2164-12-131 · Cited by 399
Li, B., Tsoi, L. C., Swindell, W. R., Gudjonsson, J. E., Tejasvi, T., Johnston, A. W. B., Ding, J., Stuart, P. E., Xing, X., Kochkodan, J. J., et al. (2014) · Journal of Investigative Dermatology · doi:10.1038/jid.2014.28 · Cited by 396
Stelpflug, S. C., Sekhon, R. S., Vaillancourt, B., Hirsch, C. N., Buell, C. R., de León, N., & Kaeppler, S. M. (2015) · The Plant Genome · doi:10.3835/plantgenome2015.04.0025 · Cited by 404
Djurišić, A. B., Leung, Y. H., Ng, A. M. C., Xu, X. Y., Lee, P. K. H., Degger, N., & Wu, R. S. S. (2014) · Small · doi:10.1002/smll.201303947 · Cited by 404
Robustly detecting differential expression in RNA sequencing data using observation weights
Zhou, X., Lindsay, H., & Robinson, M. D. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku310 · Cited by 387
Function of lncRNAs and approaches to lncRNA-protein interactions
Zhu, J., Fu, H., Wu, Y., & Zheng, X. (2013) · Science China Life Sciences · doi:10.1007/s11427-013-4553-6 · Cited by 389
Abiotic Stress - Plant Responses and Applications in Agriculture
Vahdati, K., & Leslie, C. A. (2013) · InTech eBooks · doi:10.5772/45842 · Cited by 385
Web Apollo: a web-based genomic annotation editing platform
Lee, E., Helt, G. A., Reese, J., Muñoz-Torres, M. C., Childers, C. P., Buels, R., Stein, L. D., Holmes, I. H., Elsik, C. G., & Lewis, S. (2013) · Genome biology · doi:10.1186/gb-2013-14-8-r93 · Cited by 376
Fine mapping of genome activation in bovine embryos by RNA sequencing
Graf, A., Krebs, S., Zakhartchenko, V., Schwalb, B., Blum, H., & Wolf, E. (2014) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1321569111 · Cited by 390
Shen, S., Park, J. W., Huang, J., Dittmar, K. A., Lu, Z., Zhou, Q., Carstens, R. P., & Xing, Y. (2012) · Nucleic Acids Research · doi:10.1093/nar/gkr1291 · Cited by 373
Reuse of public genome-wide gene expression data
Rung, J., & Brāzma, A. (2012) · Nature Reviews Genetics · doi:10.1038/nrg3394 · Cited by 383
Meng, J., Lu, Z., Liu, H., Zhang, L., Zhang, S., Chen, Y., Rao, M. K., & Huang, Y. (2014) · Methods · doi:10.1016/j.ymeth.2014.06.008 · Cited by 375
Selecting between-sample RNA-Seq normalization methods from the perspective of their assumptions
Evans, C., Hardin, J., & Stoebel, D. M. (2017) · Briefings in Bioinformatics · doi:10.1093/bib/bbx008 · Cited by 368
Burden-driven feedback control of gene expression
Ceroni, F., Boo, A., Furini, S., Gorochowski, T. E., Borkowski, O., Ladak, Y., Awan, A. R., Gilbert, C., Stan, G.-B. V., & Ellis, T. (2018) · Nature Methods · doi:10.1038/nmeth.4635 · Cited by 375
Gene Mapping via Bulked Segregant RNA-Seq (BSR-Seq)
Liu, S., Yeh, C., Tang, H. M., Nettleton, D. S., & Schnable, P. S. (2012) · PLoS ONE · doi:10.1371/journal.pone.0036406 · Cited by 379
Normalization, testing, and false discovery rate estimation for RNA-sequencing data
Li, J., Witten, D. M., Johnstone, I. M., & Tibshirani, R. (2012) · Biostatistics · doi:10.1093/biostatistics/kxr031 · Cited by 369
Meyer, E., Aglyamova, G. V., & Matz, M. V. (2011) · Molecular Ecology · doi:10.1111/j.1365-294x.2011.05205.x · Cited by 379
Dynamic Transcriptome Landscape of Maize Embryo and Endosperm Development
Chen, J., Zeng, B., Zhang, M., Xie, S., Wang, G., Hauck, A. L., & Lai, J. (2014) · PLANT PHYSIOLOGY · doi:10.1104/pp.114.240689 · Cited by 367
Ryabov, E. V., Wood, G. R., Fannon, J. M., Moore, J. D., Bull, J. C., Chandler, D., Mead, A., Burroughs, N. J., & Evans, D. J. (2014) · PLoS Pathogens · doi:10.1371/journal.ppat.1004230 · Cited by 363
CopraRNA and IntaRNA: predicting small RNA targets, networks and interaction domains
Wright, P. R., Georg, J., Mann, M., Sorescu, D. A., Richter, A. S., Lott, S. C., Kleinkauf, R., Hess, W. R., & Backofen, R. (2014) · Nucleic Acids Research · doi:10.1093/nar/gku359 · Cited by 364
The Expanding Landscape of Alternative Splicing Variation in Human Populations
Park, E., Pan, Z., Zhang, Z., Lin, L., & Xing, Y. (2018) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2017.11.002 · Cited by 385
Ren, S., Peng, Z., Mao, J., Yu, Y., Yin, C., Gao, X., Cui, Z., Zhang, J., Kang, Y., Xu, W., et al. (2012) · Cell Research · doi:10.1038/cr.2012.30 · Cited by 362
A Comparative Study of Techniques for Differential Expression Analysis on RNA-Seq Data
Zhang, Z. H., Jhaveri, D. J., Marshall, V. M., Bauer, D. C., Edson, J., Narayanan, R. K., Robinson, G. J., Lundberg, A. E., Bartlett, P. F., Wray, N. R., et al. (2014) · PLoS ONE · doi:10.1371/journal.pone.0103207 · Cited by 373
Next-generation sequencing for cancer diagnostics: a practical perspective.
Meldrum, C. J., Doyle, M., & Tothill, R. W. (2011) · Europe PMC (PubMed Central) · Cited by 356
Genome Editing: Targeting Susceptibility Genes for Plant Disease Resistance
Zaidi, S. S., Mukhtar, M. S., & Mansoor, S. (2018) · Trends in biotechnology · doi:10.1016/j.tibtech.2018.04.005 · Cited by 357
TSEBRA: transcript selector for BRAKER
Gabriel, L., Hoff, K. J., Brůna, T., Borodovsky, M., & Stanke, M. (2021) · BMC Bioinformatics · doi:10.1186/s12859-021-04482-0 · Cited by 410
A single-base resolution map of an archaeal transcriptomePreprint
Wurtzel, O., Sapra, R., Chen, F., Zhu, Y., Simmons, B. A., & Sorek, R. (2009) · Genome Research · doi:10.1101/gr.100396.109 · Cited by 356
Wernersson, A.-S., Carere, M., Maggi, C., Tušil, P., Soldán, P., James, A., Sánchez, W., Dulio, V., Broeg, K., Reifferscheid, G., et al. (2015) · Environmental Sciences Europe · doi:10.1186/s12302-015-0039-4 · Cited by 354
Perspectives on deciphering mechanisms underlying plant heat stress response and thermotolerance
Bokszczanin, K. Ł. (2013) · Frontiers in Plant Science · doi:10.3389/fpls.2013.00315 · Cited by 353
Understanding sequencing data as compositions: an outlook and review
Quinn, T. P., Erb, I., Richardson, M. F., & Crowley, T. M. (2018) · Bioinformatics · doi:10.1093/bioinformatics/bty175 · Cited by 372
RNA-Seq Technology and Its Application in Fish Transcriptomics
Qian, X., Ba, Y., Zhuang, Q., & Zhong, G. (2013) · OMICS A Journal of Integrative Biology · doi:10.1089/omi.2013.0110 · Cited by 350
Targeted capture in evolutionary and ecological genomics
Jones, M. R., & Good, J. M. (2015) · Molecular Ecology · doi:10.1111/mec.13304 · Cited by 370
Skene, N., & Grant, S. G. N. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00016 · Cited by 345
Computational solutions for omics data
Berger, B., Peng, J., & Singh, M. (2013) · Nature Reviews Genetics · doi:10.1038/nrg3433 · Cited by 353
Next-generation sequencing in the clinic: Promises and challenges
Xuan, J., Yu, Y., Qing, T., Guo, L., & Shi, L. M. (2012) · Cancer Letters · doi:10.1016/j.canlet.2012.11.025 · Cited by 355
Xu, Z., Peters, R. J., Weirather, J. L., Luo, H., Liao, B., Zhang, X., Zhu, Y., Ji, A., Zhang, B., Hu, S., et al. (2015) · The Plant Journal · doi:10.1111/tpj.12865 · Cited by 345
Genetic, environmental, and epigenetic factors involved in CAKUT
Nicolaou, N., Renkema, K. Y., Bongers, E. M. H. F., Giles, R. H., & Knoers, N. V. A. M. (2015) · Nature Reviews Nephrology · doi:10.1038/nrneph.2015.140 · Cited by 344
CircNet: a database of circular RNAs derived from transcriptome sequencing data
Liu, Y., Li, J., Sun, C.-H., Andrews, E. H., Chao, R.-F., Lin, F.-M., Weng, S.-L., Hsu, S., Huang, C., Cheng, C., et al. (2015) · Nucleic Acids Research · doi:10.1093/nar/gkv940 · Cited by 342
Characterization of the human ESC transcriptome by hybrid sequencing
Au, K. F., Sebastiano, V., Afshar, P. T., Durruthy, J. D., Lee, L., Williams, B. A., van Bakel, H., Schadt, E. E., Reijo-Pera, R. A., Underwood, J. G., et al. (2013) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1320101110 · Cited by 341
MORC Family ATPases Required for Heterochromatin Condensation and Gene Silencing
Moissiard, G., Cokus, S. J., Cary, J. B., Feng, S., Billi, A. C., Stroud, H., Husmann, D., Zhan, Y., Lajoie, B. R., McCord, R. P., et al. (2012) · Science · doi:10.1126/science.1221472 · Cited by 333
Optimization of de novo transcriptome assembly from next-generation sequencing data
Surget-Groba, Y., & Montoya-Burgos, J. I. (2010) · Genome Research · doi:10.1101/gr.103846.109 · Cited by 339
Shen, E., Overly, C. C., & Jones, A. R. (2012) · Trends in Neurosciences · doi:10.1016/j.tins.2012.09.005 · Cited by 333
Development and applications of single-cell transcriptome analysis
Tang, F., Lao, K., & Surani, M. A. (2011) · Nature Methods · doi:10.1038/nmeth.1557 · Cited by 342
Biomarkers in Psychiatry: Concept, Definition, Types and Relevance to the Clinical Reality
García-Gutiérrez, M. S., Navarrete, F., Sala, F., Gasparyan, A., Austrich-Olivares, A., & Manzanares, J. (2020) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2020.00432 · Cited by 331
Combining RNA-seq data and homology-based gene prediction for plants, animals and fungi
Keilwagen, J., Hartung, F., Paulini, M., Twardziok, S. O., & Grau, J. (2018) · BMC Bioinformatics · doi:10.1186/s12859-018-2203-5 · Cited by 342
Lian, J., Mishra, S., & Zhao, H. (2018) · Metabolic Engineering · doi:10.1016/j.ymben.2018.04.011 · Cited by 342
Li, Y., Ge, X., Peng, F., Li, W., & Li, J. J. (2022) · Genome Biology · doi:10.1186/s13059-022-02648-4 · Cited by 303
Detection of splice junctions from paired-end RNA-seq data by SpliceMap
Au, K. F., Jiang, H., Lin, L., Xing, Y., & Wong, W. H. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq211 · Cited by 341
Neurotoxicity in acute and repeated organophosphate exposure
Naughton, S. X., & Terry, A. V. (2018) · Toxicology · doi:10.1016/j.tox.2018.08.011 · Cited by 335
Stability, delivery and functions of human sperm RNAs at fertilization
Sendler, E. D., Johnson, G. D., Mao, S., Goodrich, R. J., Diamond, M. P., Hauser, R. B., & Krawetz, S. A. (2013) · Nucleic Acids Research · doi:10.1093/nar/gkt132 · Cited by 338
Key players in the immune response to biomaterial scaffolds for regenerative medicine
Chung, L., Maestas, D. R., Housseau, F., & Elisseeff, J. H. (2017) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2017.07.006 · Cited by 333
Candida parapsilosis: from genes to the bedside
Tóth, R., Nosek, J., Mora-Montes, H. M., Gabaldon, T., Bliss, J. M., Nosanchuk, J. D., Turner, S. A., Butler, G., Vágvölgyi, C., & Gácser, A. (2019) · Clinical Microbiology Reviews · doi:10.1128/cmr.00111-18 · Cited by 327
Global transcriptome profiles of Camellia sinensis during cold acclimation
Wang, X., Zhao, Q., Ma, C.-L., Zhang, Z. H., Cao, H., Kong, Y., Yue, C., Hao, X., Chen, L., Ma, J., et al. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-415 · Cited by 324
Promise of personalized omics to precision medicine
Chen, R., & Snyder, M. P. (2012) · WIREs Systems Biology and Medicine · doi:10.1002/wsbm.1198 · Cited by 338
Self-citationA multivariate approach to the integration of multi-omics datasets
Meng, C., Küster, B., Culhane, A. C., & Gholami, A. M. (2014) · BMC Bioinformatics · doi:10.1186/1471-2105-15-162 · Cited by 336
RNA‐Seq: A Method for Comprehensive Transcriptome Analysis
Nagalakshmi, U., Waern, K., & Snyder, M. P. (2010) · Current Protocols in Molecular Biology · doi:10.1002/0471142727.mb0411s89 · Cited by 327
Self-citationBulked sample analysis in genetics, genomics and crop improvement
Zou, C., Wang, P., & Xu, Y. (2016) · Plant Biotechnology Journal · doi:10.1111/pbi.12559 · Cited by 325
Interpretation of differential gene expression results of RNA-seq data: review and integration
McDermaid, A., Monier, B., Zhao, J., Liu, B., & Ma, Q. (2018) · Briefings in Bioinformatics · doi:10.1093/bib/bby067 · Cited by 344
Daugherty, A., Tall, A. R., Daemen, M. J. A. P., Falk, E., Fisher, E. A. A., García‐Cardeña, G., Lusis, A. J., Owens, A. P., Rosenfeld, M. E., & Virmani, R. (2017) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atv.0000000000000062 · Cited by 321
The use of skin models in drug development
Mathes, S. H., Ruffner, H., & Graf‐Hausner, U. (2014) · Advanced Drug Delivery Reviews · doi:10.1016/j.addr.2013.12.006 · Cited by 328
Shan, X., Chiang, P., Price, D. L., & Wong, P. C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1003459107 · Cited by 323
Next-generation sequencing data interpretation: enhancing reproducibility and accessibility
Nekrutenko, A., & Taylor, J. (2012) · Nature Reviews Genetics · doi:10.1038/nrg3305 · Cited by 328
FragSeq: transcriptome-wide RNA structure probing using high-throughput sequencing
Underwood, J. G., Uzilov, A. V., Katzman, S. J., Onodera, C. S., Mainzer, J. E., Mathews, D. H., Lowe, T. M., Salama, S. R., & Haussler, D. H. (2010) · Nature Methods · doi:10.1038/nmeth.1529 · Cited by 315
Historical perspective, development and applications of next-generation sequencing in plant virology
Barba, M., Czosnek, H., & Hadidi, A. (2014) · Viruses · doi:10.3390/v6010106 · Cited by 317
“[100].”
RNA-Seq identifies novel myocardial gene expression signatures of heart failure
Liu, Y., Morley, M. P., Brandimarto, J., Hannenhalli, S. S., Hu, Y., Ashley, E. A., Tang, W. H. W., Moravec, C. S., Margulies, K. B., Cappola, T. P., et al. (2014) · Genomics · doi:10.1016/j.ygeno.2014.12.002 · Cited by 324
Three Differential Expression Analysis Methods for RNA Sequencing: limma, EdgeR, DESeq2
Liu, S., Wang, Z., Zhu, R., Wang, F., Cheng, Y., & Liu, Y. (2021) · Journal of Visualized Experiments · doi:10.3791/62528 · Cited by 315
Self-citationBioJupies: Automated Generation of Interactive Notebooks for RNA-Seq Data Analysis in the Cloud
Torre, D., Lachmann, A., & Ma’ayan, A. (2018) · Cell Systems · doi:10.1016/j.cels.2018.10.007 · Cited by 301
Non‐coding RNAs: Meet thy masters
Costa, F. F. (2010) · BioEssays · doi:10.1002/bies.200900112 · Cited by 314
Long noncoding RNAs in development and disease of the central nervous system
Ng, S., Lin, L., Soh, B.-S., & Stanton, L. W. (2013) · Trends in Genetics · doi:10.1016/j.tig.2013.03.002 · Cited by 314
Cloud-scale RNA-sequencing differential expression analysis with Myrna
Langmead, B., Hansen, K. D., & Leek, J. T. (2010) · Genome biology · doi:10.1186/gb-2010-11-8-r83 · Cited by 320
SNP Discovery through Next-Generation Sequencing and Its Applications
Kumar, S. D., Banks, T. W., & Cloutier, S. (2012) · International Journal of Plant Genomics · doi:10.1155/2012/831460 · Cited by 337
Singh, R. R., Patel, K. P., Routbort, M. J., Reddy, N. G., Barkoh, B. A., Handal, B. A., Kanagal‐Shamanna, R., Greaves, W. O., Medeiros, L. J., Aldape, K., et al. (2013) · Journal of Molecular Diagnostics · doi:10.1016/j.jmoldx.2013.05.003 · Cited by 317
Direct and indirect effects of H-NS and Fis on global gene expression control in Escherichia coli
Kahramanoglou, C., Seshasayee, A. S. N., Prieto, A. I., Ibberson, D., Schmidt, S., Zimmermann, J., Beneš, V., Fraser, G. M., & Luscombe, N. M. (2010) · Nucleic Acids Research · doi:10.1093/nar/gkq934 · Cited by 312
Nattkemper, L. A., Tey, H. L., Valdés‐Rodríguez, R., Lee, H. Y., Mollanazar, N. K., Albornoz, C. A., Sanders, K. M., & Yosipovitch, G. (2018) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2017.12.029 · Cited by 310
The role of alternative splicing in cancer: From oncogenesis to drug resistance
Sciarrillo, R., Wojtuszkiewicz, A., Assaraf, Y. G., Jansen, G., Kaspers, G. J. L., Giovannetti, E., & Cloos, J. J. (2020) · Drug Resistance Updates · doi:10.1016/j.drup.2020.100728 · Cited by 317
Nookaew, I., Papini, M., Pornputtapong, N., Scalcinati, G., Fagerberg, L., Uhlén, M., & Nielsen, J. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks804 · Cited by 309
Cumulus and granulosa cell markers of oocyte and embryo quality
Uyar, A., Torrealday, S., & Seli, E. U. (2013) · Fertility and Sterility · doi:10.1016/j.fertnstert.2013.01.129 · Cited by 317
Transcribed dark matter: meaning or myth?
Ponting, C. P., & Belgard, T. G. (2010) · Human Molecular Genetics · doi:10.1093/hmg/ddq362 · Cited by 315
High‐throughput sequencing for biology and medicine
Soon, W. W., Hariharan, M., & Snyder, M. P. (2013) · Molecular Systems Biology · doi:10.1038/msb.2012.61 · Cited by 313
Self-citationSystems biology in cardiovascular disease: a multiomics approach
Joshi, A., Rienks, M., Theofilatos, K., & Mayr, M. (2020) · Nature Reviews Cardiology · doi:10.1038/s41569-020-00477-1 · Cited by 309
Scheben, A., Batley, J., & Edwards, D. (2016) · Plant Biotechnology Journal · doi:10.1111/pbi.12645 · Cited by 323
Expression Profile of Ectopic Olfactory Receptors Determined by Deep Sequencing
Flegel, C., Manteniotis, S., Osthold, S., Hatt, H. H., & Gisselmann, G. (2013) · PLoS ONE · doi:10.1371/journal.pone.0055368 · Cited by 306
Implementing personalized cancer genomics in clinical trials
Simon, R. M., & Roychowdhury, S. (2013) · Nature Reviews Drug Discovery · doi:10.1038/nrd3979 · Cited by 309
Waters, B. M., & Sankaran, R. P. (2010) · Plant Science · doi:10.1016/j.plantsci.2010.12.003 · Cited by 301
Becker, J., & Wittmann, C. (2015) · Angewandte Chemie International Edition · doi:10.1002/anie.201409033 · Cited by 295
Vitamin D Receptor Signaling Mechanisms: Integrated Actions of a Well-Defined Transcription Factor
Carlberg, C., & Campbell, M. J. (2013) · Steroids · doi:10.1016/j.steroids.2012.10.019 · Cited by 293
Simultaneous generation of many RNA-seq libraries in a single reaction
Shishkin, A. A., Giannoukos, G., Küçükural, A., Ciulla, D., Busby, M., Surka, C., Chen, J., Bhattacharyya, R. P., Rudy, R. F., Patel, M. M., et al. (2015) · Nature Methods · doi:10.1038/nmeth.3313 · Cited by 288
Prospects and challenges of multi-omics data integration in toxicology
Canzler, S., Schor, J., Busch, W., Schubert, K. A., Rolle-Kampczyk, U. E., Seitz, H., Kamp, H., von Bergen�, M., Buesen, R., & Hackermüller, J. (2020) · Archives of Toxicology · doi:10.1007/s00204-020-02656-y · Cited by 300
Integrated omics analysis of specialized metabolism in medicinal plants
Rai, A., Saito, K., & Yamazaki, M. (2017) · The Plant Journal · doi:10.1111/tpj.13485 · Cited by 303
RNA sequencing reveals two major classes of gene expression levels in metazoan cells
Hebenstreit, D., Fang, M., Gu, M., Charoensawan, V., van Oudenaarden, A., & Teichmann, S. A. (2011) · Molecular Systems Biology · doi:10.1038/msb.2011.28 · Cited by 289
Transcriptome Profiling in Human Diseases: New Advances and Perspectives
Casamassimi, A., Federico, A., Rienzo, M., Esposito, S., & Ciccodicola, A. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18081652 · Cited by 297
Nielsen, L. B., Wang, C., Sørensen, K., Bang‐Berthelsen, C. H., Hansen, L. B., Andersen, M.-L. M., Hougaard, P., Juul, A., Zhang, C., Pociot, F., et al. (2012) · Experimental Diabetes Research · doi:10.1155/2012/896362 · Cited by 289
Bridger: a new framework for de novo transcriptome assembly using RNA-seq data
Chang, Z., Li, G., Liu, J., Zhang, Y., Ashby, C., Liu, D., Cramer, C. L., & Huang, X. (2015) · Genome biology · doi:10.1186/s13059-015-0596-2 · Cited by 292
Kapranov, P., Laurent, G. S., Raz, T., Ozsolak, F., Reynolds, C. P., Sorensen, P. H. B., Reaman, G. H., Milos, P. M., Arceci, R. J., Thompson, J. F., et al. (2010) · BMC Biology · doi:10.1186/1741-7007-8-149 · Cited by 288
The Role of Natural Killer Cells in Autoimmune Diseases
Küçüksezer, U. C., Çetin, E. A., Esen, F., Tahralı, İ., Akdeniz, N., Gelmez, M. Y., & Deniz, G. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.622306 · Cited by 304
RNA-seq: technical variability and sampling
McIntyre, L. M., Lopiano, K. K., Morse, A. M., Amin, V., Oberg, A. L., Young, L. J., & Nuzhdin, S. V. (2011) · BMC Genomics · doi:10.1186/1471-2164-12-293 · Cited by 285
Trick, M., Adamski, N. M., Mugford, S. G., Jiang, C., Febrer, M., & Uauy, C. (2012) · BMC Plant Biology · doi:10.1186/1471-2229-12-14 · Cited by 281
Metadata
- Authors
- Wang, Z., Gerstein, M., & Snyder, M.
- Affiliations
- Yale University (US)
- Corresponding author
- Snyder, Michael
- Venue
- Nature Reviews Genetics
- Published
- 2009-01
- Volume
- 10
- Issue
- 1
- Pages
- 57-63
- ISSN
- 1471-0056 (ISSN-L)
- 1471-0064
- PMC
- PMC2949280
- OpenAlex
- W1981509058
- Cited by
- 13,174
- References
- 44
- Citations by year
- 2026: 518 · 2025: 745 · 2024: 728 · 2023: 662 · 2022: 856 · 2021: 974 · 2020: 916 · 2019: 862 · 2018: 911 · 2017: 867 · 2016: 901 · 2015: 960 · 2014: 900 · 2013: 815 · 2012: 662
- FWCI
- 22.07
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature Reviews Genetics (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Human Genome Research Institute (P50HG002357)
- National Cancer Institute (R01CA077808)
- 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 › RNA Research and Splicing
- Keywords
- RNA-seq, transcriptomics, gene expression profiling, deep sequencing, mRNA isoforms, transcript quantification, next-generation sequencing
- MeSH terms
- Animals, Base Sequence, Chromosome Mapping, Exons, Humans, Models, Genetic, Molecular Sequence Data, RNA, Transcription, Genetic, Sequence Analysis, RNA, Gene Expression Profiling
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review