Counting absolute numbers of molecules using unique molecular identifiers
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S. Linnarsson | Martin Enge | T. Kivioja | J. Taipale | M. Bonke | Anna Vähärautio | Kasper Karlsson | M. Enge | Teemu Kivioja | Martin Bonke
[1] Syr Hui,et al. US Patent Application , 2013 .
[2] K. Kinzler,et al. Detection and quantification of rare mutations with massively parallel sequencing , 2011, Proceedings of the National Academy of Sciences.
[3] S. P. Fodor,et al. Counting individual DNA molecules by the stochastic attachment of diverse labels , 2011, Proceedings of the National Academy of Sciences.
[4] James A. Casbon,et al. A method for counting PCR template molecules with application to next-generation sequencing , 2011, Nucleic acids research.
[5] Fatih Ozsolak,et al. RNA sequencing: advances, challenges and opportunities , 2011, Nature Reviews Genetics.
[6] Michael Briese,et al. iCLIP Predicts the Dual Splicing Effects of TIA-RNA Interactions , 2010, PLoS biology.
[7] B. Wittner,et al. Amplification-free digital gene expression profiling from minute cell quantities , 2010, Nature Methods.
[8] N. Friedman,et al. Comprehensive comparative analysis of strand-specific RNA sequencing methods , 2010, Nature Methods.
[9] J. Ule,et al. iCLIP reveals the function of hnRNP particles in splicing at individual nucleotide resolution , 2010, Nature Structural &Molecular Biology.
[10] S. Linnarsson. Recent advances in DNA sequencing methods - general principles of sample preparation. , 2010, Experimental cell research.
[11] W. Huber,et al. which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. MAnorm: a robust model for quantitative comparison of ChIP-Seq data sets , 2011 .
[12] Jeffrey G. Reifenberger,et al. Direct RNA sequencing , 2009, Nature.
[13] S. Letovsky,et al. Quantification of the yeast transcriptome by single-molecule sequencing , 2009, Nature Biotechnology.
[14] Richard Durbin,et al. Sequence analysis Fast and accurate short read alignment with Burrows – Wheeler transform , 2009 .
[15] Cole Trapnell,et al. Ultrafast and memory-efficient alignment of short DNA sequences to the human genome , 2009, Genome Biology.
[16] C. Cantor,et al. Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma , 2008, Proceedings of the National Academy of Sciences.
[17] H. C. Fan,et al. Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood , 2008, Proceedings of the National Academy of Sciences.
[18] S. Ranade,et al. Stem cell transcriptome profiling via massive-scale mRNA sequencing , 2008, Nature Methods.
[19] H. Koltai,et al. Specificity of DNA microarray hybridization: characterization, effectors and approaches for data correction , 2008, Nucleic acids research.
[20] R. Rigby,et al. Generalized Additive Models for Location Scale and Shape (GAMLSS) in R , 2007 .
[21] J. Hoheisel. Microarray technology: beyond transcript profiling and genotype analysis , 2006, Nature Reviews Microbiology.
[22] James R. Knight,et al. Genome sequencing in microfabricated high-density picolitre reactors , 2005, Nature.
[23] J. Shendure,et al. Materials and Methods Som Text Figs. S1 and S2 Tables S1 to S4 References Accurate Multiplex Polony Sequencing of an Evolved Bacterial Genome , 2022 .
[24] Jihn E. Kim,et al. Gauge unification via stable brane recombination , 2005, hep-th/0508149.
[25] S. Lukyanov,et al. Simple cDNA normalization using kamchatka crab duplex-specific nuclease. , 2004, Nucleic acids research.
[26] Ian Humphery-Smith,et al. Regionalized GC content of template DNA as a predictor of PCR success. , 2003, Nucleic acids research.
[27] H. Hug,et al. Measurement of the number of molecules of a single mRNA species in a complex mRNA preparation. , 2003, Journal of theoretical biology.
[28] M. Holland,et al. Transcript Abundance in Yeast Varies over Six Orders of Magnitude* , 2002, The Journal of Biological Chemistry.
[29] A. Chenchik,et al. Reverse transcriptase template switching: a SMART approach for full-length cDNA library construction. , 2001, BioTechniques.
[30] Jiasen Lu,et al. Assessment of the sensitivity and specificity of oligonucleotide (50mer) microarrays. , 2000, Nucleic acids research.
[31] K. Kinzler,et al. Digital PCR. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[32] K. Kinzler,et al. Serial Analysis of Gene Expression , 1995, Science.
[33] Ronald W. Davis,et al. Quantitative Monitoring of Gene Expression Patterns with a Complementary DNA Microarray , 1995, Science.
[34] Kousaku Okubo,et al. Large scale cDNA sequencing for analysis of quantitative and qualitative aspects of gene expression , 1992, Nature Genetics.
[35] S. Weissman,et al. Construction of a uniform-abundance (normalized) cDNA library. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[36] K. Mullis,et al. Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia. , 1985, Science.
[37] W. Gilbert,et al. A new method for sequencing DNA. , 1977, Proceedings of the National Academy of Sciences of the United States of America.
[38] F. Sanger,et al. A rapid method for determining sequences in DNA by primed synthesis with DNA polymerase. , 1975, Journal of molecular biology.
[39] A. C. Chang,et al. Construction of biologically functional bacterial plasmids in vitro. , 1973, Proceedings of the National Academy of Sciences of the United States of America.