Evaluation of SNP calling methods for closely related bacterial isolates and a novel high-accuracy pipeline: BactSNP
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Tetsuya Hayashi | T. Itoh | Y. Ogura | Rei Kajitani | Yasuhiro Gotoh | D. Yoshimura | Miki Okuno | K. Katahira | Yoshitoshi Ogura
[1] H. Chu,et al. The role of recombination in evolutionary adaptation of Escherichia coli to a novel nutrient , 2017, Journal of evolutionary biology.
[2] Lorin D. Warnick,et al. Whole-Genome Sequencing of Drug-Resistant Salmonella enterica Isolates from Dairy Cattle and Humans in New York and Washington States Reveals Source and Geographic Associations , 2017, Applied and Environmental Microbiology.
[3] J. Parkhill,et al. Evolution and Epidemiology of Multidrug-Resistant Klebsiella pneumoniae in the United Kingdom and Ireland , 2017, mBio.
[4] C. Buchrieser,et al. Multiple major disease-associated clones of Legionella pneumophila have emerged recently and independently , 2016, Genome research.
[5] Maliha Aziz,et al. NASP: an accurate, rapid method for the identification of SNPs in WGS datasets that supports flexible input and output formats. , 2016, Microbial genomics.
[6] Brian T. Tsuji,et al. Polymyxin Resistance in Acinetobacter baumannii: Genetic Mutations and Transcriptomic Changes in Response to Clinically Relevant Dosage Regimens , 2016, Scientific Reports.
[7] Y. Teo,et al. Genetic signatures of Mycobacterium tuberculosis Nonthaburi genotype revealed by whole genome analysis of isolates from tuberculous meningitis patients in Thailand , 2016, PeerJ.
[8] E. J. McTavish,et al. TreeToReads - a pipeline for simulating raw reads from phylogenies , 2016, bioRxiv.
[9] R. Olsen,et al. A molecular trigger for intercontinental epidemics of group A Streptococcus. , 2015, The Journal of clinical investigation.
[10] Yan Luo,et al. CFSAN SNP Pipeline: an automated method for constructing SNP matrices from next-generation sequence data , 2015, PeerJ Comput. Sci..
[11] L. Hurst,et al. Genomic analysis of isolates from the United Kingdom 2012 pertussis outbreak reveals that vaccine antigen genes are unusually fast evolving. , 2015, The Journal of infectious diseases.
[12] M. Wiedmann,et al. Whole-Genome Sequencing Allows for Improved Identification of Persistent Listeria monocytogenes in Food-Associated Environments , 2015, Applied and Environmental Microbiology.
[13] A. Buckling,et al. Coevolution with bacteriophages drives genome-wide host evolution and constrains the acquisition of abiotic-beneficial mutations. , 2015, Molecular biology and evolution.
[14] Jacqueline A. Keane,et al. Rapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins , 2014, Nucleic acids research.
[15] Julian Parkhill,et al. Emergence of a New Epidemic Neisseria meningitidis Serogroup A Clone in the African Meningitis Belt: High-Resolution Picture of Genomic Changes That Mediate Immune Evasion , 2014, mBio.
[16] B. Shapiro,et al. Evolutionary consequences of intra-patient phage predation on microbial populations , 2014, eLife.
[17] Tetsuya Hayashi,et al. Efficient de novo assembly of highly heterozygous genomes from whole-genome shotgun short reads , 2014, Genome research.
[18] Heng Li. Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM , 2013, 1303.3997.
[19] Julian Parkhill,et al. Whole-genome sequencing for analysis of an outbreak of meticillin-resistant Staphylococcus aureus: a descriptive study , 2013, The Lancet. Infectious Diseases.
[20] Daniel J. Wilson,et al. Whole-genome sequencing to delineate Mycobacterium tuberculosis outbreaks: a retrospective observational study , 2013, The Lancet. Infectious diseases.
[21] Gabor T. Marth,et al. Haplotype-based variant detection from short-read sequencing , 2012, 1207.3907.
[22] Christopher A. Miller,et al. VarScan 2: somatic mutation and copy number alteration discovery in cancer by exome sequencing. , 2012, Genome research.
[23] Leping Li,et al. ART: a next-generation sequencing read simulator , 2012, Bioinform..
[24] G. McVean,et al. De novo assembly and genotyping of variants using colored de Bruijn graphs , 2011, Nature Genetics.
[25] Heng Li,et al. A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data , 2011, Bioinform..
[26] Martin Goodson,et al. Stampy: a statistical algorithm for sensitive and fast mapping of Illumina sequence reads. , 2011, Genome research.
[27] M. DePristo,et al. A framework for variation discovery and genotyping using next-generation DNA sequencing data , 2011, Nature Genetics.
[28] Helga Thorvaldsdóttir,et al. Integrative Genomics Viewer , 2011, Nature Biotechnology.
[29] A. Cheung,et al. Faculty Opinions recommendation of Evolution of MRSA during hospital transmission and intercontinental spread. , 2010 .
[30] Gonçalo R. Abecasis,et al. The Sequence Alignment/Map format and SAMtools , 2009, Bioinform..
[31] B. Hall,et al. Simulating DNA coding sequence evolution with EvolveAGene 3. , 2008, Molecular biology and evolution.
[32] Michael P. Cummings,et al. PAUP* [Phylogenetic Analysis Using Parsimony (and Other Methods)] , 2004 .
[33] S. Salzberg,et al. Versatile and open software for comparing large genomes , 2004, Genome Biology.
[34] 田中 俊典. National Center for Biotechnology Information (NCBI) , 2012 .