ShortRead: a bioconductor package for input, quality assessment and exploration of high-throughput sequence data

作者: M. Morgan , S. Anders , M. Lawrence , P. Aboyoun , H. Pages

DOI: 10.1093/BIOINFORMATICS/BTP450

关键词: Quality assessmentGene expression profilingBioconductorHigh throughput sequenceDatabaseData transformationQuality (business)Computer scienceHigh-throughput screening

摘要: Summary: ShortRead is a package for input, quality assessment, manipulation and output of high-throughput sequencing data. provided in the R Bioconductor environments, allowing ready access to additional facilities advanced statistical analysis, data transformation, visualization integration with diverse genomic resources. Availability Implementation: This implemented available at web site; contains ‘vignette’ outlining typical work flows. Contact: mtmorgan@fhcrc.org

参考文章(10)
David R Bentley, Shankar Balasubramanian, Harold P Swerdlow, Geoffrey P Smith, John Milton, Clive G Brown, Kevin P Hall, Dirk J Evers, Colin L Barnes, Helen R Bignell, Jonathan M Boutell, Jason Bryant, Richard J Carter, R Keira Cheetham, Anthony J Cox, Darren J Ellis, Michael R Flatbush, Niall A Gormley, Sean J Humphray, Leslie J Irving, Mirian S Karbelashvili, Scott M Kirk, Heng Li, Xiaohai Liu, Klaus S Maisinger, Lisa J Murray, Bojan Obradovic, Tobias Ost, Michael L Parkinson, Mark R Pratt, Isabelle MJ Rasolonjatovo, Mark T Reed, Roberto Rigatti, Chiara Rodighiero, Mark T Ross, Andrea Sabot, Subramanian V Sankar, Aylwyn Scally, Gary P Schroth, Mark E Smith, Vincent P Smith, Anastassia Spiridou, Peta E Torrance, Svilen S Tzonev, Eric H Vermaas, Klaudia Walter, Xiaolin Wu, Lu Zhang, Mohammed D Alam, Carole Anastasi, Ify C Aniebo, David MD Bailey, Iain R Bancarz, Saibal Banerjee, Selena G Barbour, Primo A Baybayan, Vincent A Benoit, Kevin F Benson, Claire Bevis, Phillip J Black, Asha Boodhun, Joe S Brennan, John A Bridgham, Rob C Brown, Andrew A Brown, Dale H Buermann, Abass A Bundu, James C Burrows, Nigel P Carter, Nestor Castillo, Maria Chiara E. Catenazzi, Simon Chang, R Neil Cooley, Natasha R Crake, Olubunmi O Dada, Konstantinos D Diakoumakos, Belen Dominguez-Fernandez, David J Earnshaw, Ugonna C Egbujor, David W Elmore, Sergey S Etchin, Mark R Ewan, Milan Fedurco, Louise J Fraser, Karin V Fuentes Fajardo, W Scott Furey, David George, Kimberley J Gietzen, Colin P Goddard, George S Golda, Philip A Granieri, David E Green, David L Gustafson, Nancy F Hansen, Kevin Harnish, Christian D Haudenschild, Narinder I Heyer, Matthew M Hims, Johnny T Ho, Adrian M Horgan, Katya Hoschler, Steve Hurwitz, Denis V Ivanov, Maria Q Johnson, Terena James, TA Huw Jones, Gyoung-Dong Kang, Tzvetana H Kerelska, Alan D Kersey, Irina Khrebtukova, Alex P Kindwall, Zoya Kingsbury, Paula I Kokko-Gonzales, Anil Kumar, Marc A Laurent, Cynthia T Lawley, Sarah E Lee, Xavier Lee, Arnold K Liao, Jennifer A Loch, Mitch Lok, Shujun Luo, Radhika M Mammen, John W Martin, Patrick G McCauley, Paul McNitt, Parul Mehta, Keith W Moon, Joe W Mullens, Taksina Newington, Zemin Ning, Bee Ling Ng, Sonia M Novo, Michael J O’Neill, Mark A Osborne, Andrew Osnowski, Omead Ostadan, Lambros L Paraschos, Lea Pickering, Andrew C Pike, Alger C Pike, D Chris Pinkard, Daniel P Pliskin, Joe Podhasky, Victor J Quijano, Come Raczy, Vicki H Rae, Stephen R Rawlings, Ana Chiva Rodriguez, Phyllida M Roe, None, Accurate whole human genome sequencing using reversible terminator chemistry Nature. ,vol. 456, pp. 53- 59 ,(2008) , 10.1038/NATURE07517
Elaine R Mardis, ChIP-seq: welcome to the new frontier. Nature Methods. ,vol. 4, pp. 613- 614 ,(2007) , 10.1038/NMETH0807-613
Peter V Kharchenko, Michael Y Tolstorukov, Peter J Park, Design and analysis of ChIP-seq experiments for DNA-binding proteins Nature Biotechnology. ,vol. 26, pp. 1351- 1359 ,(2008) , 10.1038/NBT.1508
H. Li, J. Ruan, R. Durbin, Mapping short DNA sequencing reads and calling variants using mapping quality scores Genome Research. ,vol. 18, pp. 1851- 1858 ,(2008) , 10.1101/GR.078212.108
T. T. Torres, M. Metta, B. Ottenwalder, C. Schlotterer, Gene expression profiling by massively parallel sequencing Genome Research. ,vol. 18, pp. 172- 177 ,(2007) , 10.1101/GR.6984908
Ben Langmead, Cole Trapnell, Mihai Pop, Steven L Salzberg, Ultrafast and memory-efficient alignment of short DNA sequences to the human genome Genome Biology. ,vol. 10, pp. 1- 10 ,(2009) , 10.1186/GB-2009-10-3-R25
P. A. Fujita, B. Rhead, A. S. Zweig, A. S. Hinrichs, D. Karolchik, M. S. Cline, M. Goldman, G. P. Barber, H. Clawson, A. Coelho, M. Diekhans, T. R. Dreszer, B. M. Giardine, R. A. Harte, J. Hillman-Jackson, F. Hsu, V. Kirkup, R. M. Kuhn, K. Learned, C. H. Li, L. R. Meyer, A. Pohl, B. J. Raney, K. R. Rosenbloom, K. E. Smith, D. Haussler, W. J. Kent, The UCSC Genome Browser database: update 2011 Nucleic Acids Research. ,vol. 39, pp. 876- 882 ,(2011) , 10.1093/NAR/GKQ963
Ali Mortazavi, Brian A Williams, Kenneth McCue, Lorian Schaeffer, Barbara Wold, Mapping and quantifying mammalian transcriptomes by RNA-Seq Nature Methods. ,vol. 5, pp. 621- 628 ,(2008) , 10.1038/NMETH.1226
Robert C Gentleman, Vincent J Carey, Douglas M Bates, Ben Bolstad, Marcel Dettling, Sandrine Dudoit, Byron Ellis, Laurent Gautier, Yongchao Ge, Jeff Gentry, Kurt Hornik, Torsten Hothorn, Wolfgang Huber, Stefano Iacus, Rafael Irizarry, Friedrich Leisch, Cheng Li, Martin Maechler, Anthony J Rossini, Gunther Sawitzki, Colin Smith, Gordon Smyth, Luke Tierney, Jean YH Yang, Jianhua Zhang, None, Bioconductor: open software development for computational biology and bioinformatics Genome Biology. ,vol. 5, pp. 1- 16 ,(2004) , 10.1186/GB-2004-5-10-R80
R. M. Kuhn, D. Karolchik, A. S. Zweig, T. Wang, K. E. Smith, K. R. Rosenbloom, B. Rhead, B. J. Raney, A. Pohl, M. Pheasant, L. Meyer, F. Hsu, A. S. Hinrichs, R. A. Harte, B. Giardine, P. Fujita, M. Diekhans, T. Dreszer, H. Clawson, G. P. Barber, D. Haussler, W. J. Kent, The UCSC Genome Browser Database: update 2009 Nucleic Acids Research. ,vol. 37, pp. 755- 761 ,(2009) , 10.1093/NAR/GKN875