Modeling non-uniformity in short-read rates in RNA-Seq data
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[1] International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome , 2001, Nature.
[2] J. Friedman. Greedy function approximation: A gradient boosting machine. , 2001 .
[3] J. Hardin,et al. Generalized Linear Models and Extensions , 2001 .
[4] Mouse Genome Sequencing Consortium. Initial sequencing and comparative analysis of the mouse genome , 2002, Nature.
[5] J. Friedman. Stochastic gradient boosting , 2002 .
[6] Felix Naef,et al. Solving the riddle of the bright mismatches: labeling and effective binding in oligonucleotide arrays. , 2002, Physical review. E, Statistical, nonlinear, and soft matter physics.
[7] T. Speed,et al. Summaries of Affymetrix GeneChip probe level data. , 2003, Nucleic acids research.
[8] Rafael A. Irizarry,et al. A Model-Based Background Adjustment for Oligonucleotide Expression Arrays , 2004 .
[9] B. Frey,et al. Revealing global regulatory features of mammalian alternative splicing using a quantitative microarray platform. , 2004, Molecular cell.
[10] Greg Ridgeway,et al. Generalized Boosted Models: A guide to the gbm package , 2006 .
[11] Michal J. Okoniewski,et al. Hybridization interactions between probesets in short oligo microarrays lead to spurious correlations , 2006, BMC Bioinformatics.
[12] Clifford A. Meyer,et al. Model-based analysis of tiling-arrays for ChIP-chip , 2006, Proceedings of the National Academy of Sciences.
[13] Thomas E. Royce,et al. Toward a universal microarray: prediction of gene expression through nearest-neighbor probe sequence identification , 2007, Nucleic acids research.
[14] Wei Li,et al. Model-based analysis of two-color arrays (MA2C) , 2007, Genome Biology.
[15] Dustin P. Potter,et al. Probe signal correction for differential methylation hybridization experiments , 2008, BMC Bioinformatics.
[16] Ryan D. Morin,et al. Profiling the HeLa S3 transcriptome using randomly primed cDNA and massively parallel short-read sequencing. , 2008, BioTechniques.
[17] Brian D. Ondov,et al. Efficient mapping of Applied Biosystems SOLiD sequence data to a reference genome for functional genomic applications , 2008, Bioinform..
[18] Wing Hung Wong,et al. SeqMap: mapping massive amount of oligonucleotides to the genome , 2008, Bioinform..
[19] M. Stephens,et al. RNA-seq: an assessment of technical reproducibility and comparison with gene expression arrays. , 2008, Genome research.
[20] S. Ranade,et al. Stem cell transcriptome profiling via massive-scale mRNA sequencing , 2008, Nature Methods.
[21] Eric T. Wang,et al. Alternative Isoform Regulation in Human Tissue Transcriptomes , 2008, Nature.
[22] R. Lister,et al. Highly Integrated Single-Base Resolution Maps of the Epigenome in Arabidopsis , 2008, Cell.
[23] Juliane C. Dohm,et al. Substantial biases in ultra-short read data sets from high-throughput DNA sequencing , 2008, Nucleic acids research.
[24] M. Gerstein,et al. The Transcriptional Landscape of the Yeast Genome Defined by RNA Sequencing , 2008, Science.
[25] B. Frey,et al. Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing , 2008, Nature Genetics.
[26] Robert A Holt,et al. The new paradigm of flow cell sequencing. , 2008, Genome research.
[27] I. Goodhead,et al. Dynamic repertoire of a eukaryotic transcriptome surveyed at single-nucleotide resolution , 2008, Nature.
[28] Wing Hung Wong,et al. Cross-hybridization modeling on Affymetrix exon arrays , 2008, Bioinform..
[29] B. Williams,et al. Mapping and quantifying mammalian transcriptomes by RNA-Seq , 2008, Nature Methods.
[30] Wing Hung Wong,et al. Statistical inferences for isoform expression in RNA-Seq , 2009, Bioinform..
[31] M. Gerstein,et al. RNA-Seq: a revolutionary tool for transcriptomics , 2009, Nature Reviews Genetics.
[32] W. J. Kent,et al. The UCSC Genome Browser , 2003, Current protocols in bioinformatics.
[33] K. Hansen,et al. Biases in Illumina transcriptome sequencing caused by random hexamer priming , 2010, Nucleic acids research.