Performance comparison of benchtop high-throughput sequencing platforms
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[1] S. Eddy,et al. tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. , 1997, Nucleic acids research.
[2] P Green,et al. Base-calling of automated sequencer traces using phred. II. Error probabilities. , 1998, Genome research.
[3] P. Green,et al. Base-calling of automated sequencer traces using phred. I. Accuracy assessment. , 1998, Genome research.
[4] Peter F. Hallin,et al. RNAmmer: consistent and rapid annotation of ribosomal RNA genes , 2007, Nucleic acids research.
[5] Steven Salzberg,et al. Identifying bacterial genes and endosymbiont DNA with Glimmer , 2007, Bioinform..
[6] Nancy F. Hansen,et al. Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry , 2008, Nature.
[7] Mark J. Pallen,et al. xBASE2: a comprehensive resource for comparative bacterial genomics , 2007, Nucleic Acids Res..
[8] A. Danchin,et al. Organised Genome Dynamics in the Escherichia coli Species Results in Highly Diverse Adaptive Paths , 2009, PLoS genetics.
[9] Mihai Pop,et al. Assembly complexity of prokaryotic genomes using short reads , 2010, BMC Bioinformatics.
[10] Gonçalo R. Abecasis,et al. The Sequence Alignment/Map format and SAMtools , 2009, Bioinform..
[11] Richard Durbin,et al. Sequence analysis Fast and accurate short read alignment with Burrows – Wheeler transform , 2009 .
[12] M. DePristo,et al. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. , 2010, Genome research.
[13] Paul D. Shaw,et al. BIOINFORMATICS APPLICATIONS NOTE , 2022 .
[14] M. Metzker. Sequencing technologies — the next generation , 2010, Nature Reviews Genetics.
[15] Nicholas J Loman,et al. High-throughput sequencing and clinical microbiology: progress, opportunities and challenges. , 2010, Current opinion in microbiology.
[16] Richard Durbin,et al. Fast and accurate long-read alignment with Burrows–Wheeler transform , 2010, Bioinform..
[17] Junhua Li,et al. Open-source genomic analysis of Shiga-toxin-producing E. coli O104:H4. , 2011, The New England journal of medicine.
[18] J. Rothberg,et al. Prospective Genomic Characterization of the German Enterohemorrhagic Escherichia coli O104:H4 Outbreak by Rapid Next Generation Sequencing Technology , 2011, PloS one.
[19] E. Brzuszkiewicz,et al. Genome sequence analyses of two isolates from the recent Escherichia coli outbreak in Germany reveal the emergence of a new pathotype: Entero-Aggregative-Haemorrhagic Escherichia coli (EAHEC) , 2011, Archives of Microbiology.
[20] James H. Bullard,et al. Origins of the E. coli strain causing an outbreak of hemolytic-uremic syndrome in Germany. , 2011, The New England journal of medicine.
[21] T. Glenn. Field guide to next‐generation DNA sequencers , 2011, Molecular ecology resources.
[22] T. Dallman,et al. Enteroaggregative E. coli O104 from an outbreak of HUS in Germany 2011, could it happen again? , 2011, Journal of infection in developing countries.
[23] Klaus Stark,et al. Epidemic profile of Shiga-toxin-producing Escherichia coli O104:H4 outbreak in Germany. , 2011, The New England journal of medicine.
[24] Bernard P. Puc,et al. An integrated semiconductor device enabling non-optical genome sequencing , 2011, Nature.
[25] Marc T. Facciotti,et al. Mauve Assembly Metrics , 2011, Bioinform..
[26] Eric S. Lander,et al. Genomic epidemiology of the Escherichia coli O104:H4 outbreaks in Europe, 2011 , 2012, Proceedings of the National Academy of Sciences.