Improvements to PATRIC, the all-bacterial Bioinformatics Database and Analysis Resource Center.
Improvements to PATRIC, the all-bacterial Bioinformatics Database and Analysis Resource Center.
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DOI:
10.1093/nar/gkw1017
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发表时间:
2017-01-04
影响因子:
14.9
通讯作者:
Stevens RL
中科院分区:
文献类型:
--
作者:
Wattam AR;Davis JJ;Assaf R;Boisvert S;Brettin T;Bun C;Conrad N;Dietrich EM;Disz T;Gabbard JL;Gerdes S;Henry CS;Kenyon RW;Machi D;Mao C;Nordberg EK;Olsen GJ;Murphy-Olson DE;Olson R;Overbeek R;Parrello B;Pusch GD;Shukla M;Vonstein V;Warren A;Xia F;Yoo H;Stevens RL
The Pathosystems Resource Integration Center (PATRIC) is the bacterial Bioinformatics Resource Center (https://www.patricbrc.org). Recent changes to PATRIC include a redesign of the web interface and some new services that provide users with a platform that takes them from raw reads to an integrated analysis experience. The redesigned interface allows researchers direct access to tools and data, and the emphasis has changed to user-created genome-groups, with detailed summaries and views of the data that researchers have selected. Perhaps the biggest change has been the enhanced capability for researchers to analyze their private data and compare it to the available public data. Researchers can assemble their raw sequence reads and annotate the contigs using RASTtk. PATRIC also provides services for RNA-Seq, variation, model reconstruction and differential expression analysis, all delivered through an updated private workspace. Private data can be compared by ‘virtual integration’ to any of PATRIC's public data. The number of genomes available for comparison in PATRIC has expanded to over 80 000, with a special emphasis on genomes with antimicrobial resistance data. PATRIC uses this data to improve both subsystem annotation and k-mer classification, and tags new genomes as having signatures that indicate susceptibility or resistance to specific antibiotics.
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影响因子:
48
作者:
Langmead, Ben;Salzberg, Steven L.
通讯作者:
Salzberg, Steven L.
影响因子:
4.6
作者:
Davis JJ;Boisvert S;Brettin T;Kenyon RW;Mao C;Olson R;Overbeek R;Santerre J;Shukla M;Wattam AR;Will R;Xia F;Stevens R
通讯作者:
Stevens R
影响因子:
14.9
作者:
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Kodama Y;Shumway M;Leinonen R;International Nucleotide Sequence Database Collaboration
通讯作者:
International Nucleotide Sequence Database Collaboration
影响因子:
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作者:
Frith MC;Wan R;Horton P
通讯作者:
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