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1 RAST incorporated with an empirical four-parameter equat
2 (p = 0.0004) and house dust mite (p = 0.04), RAST to grass (p = 0.002) and bronchial reactivity to me
4 ls were then built and compared with AST and RAST, based on which a new modeling strategy coupling FN
5 interconnectedness of the SEED database and RAST, the RAST annotation pipeline and updates to both r
9 RMSE = 0.10), which is comparable to that by RAST (0.10) and much lower than those by AST (0.26) and
12 square error (RMSE) of predictions by the FN-RAST is 0.082 log units for 50 bisolute adsorption on MN
16 the reporting of AST results was 39.2 h for RAST and 44.4 h for NAST (5.2 h faster for RAST [P = 0.0
19 ge variable cost was $4, 927 per patient for RAST and $6,677 for NAST, a difference of $1,750 less pe
20 length of stay was 10.7 days per patient for RAST and 12.6 days for NAST, a difference of 2.0 days le
21 h sera from CM-allergic patients (n = 26) in RAST-based assays and with rat basophils transfected wit
25 houses abstract data types, the metagenomics RAST is stable, extensible, and freely available to all
27 ent through our experience with metagenomics-RAST (MG-RAST), the most popular metagenomics analysis p
30 were analyzed through PathoScope (PS) and MG-RAST (MR), and mapped to 380 bacterial, 56 archaeal, and
32 n popular metagenomics resources, such as MG-RAST, EBI Metagenomics, and probeBASE, as well as a newl
33 ce of various bioinformatic tools (BLAST, MG-RAST, NBC, VMGAP, MetaVir, VIROME) for analysing the vir
34 phylogenetic analysis of these contigs by MG-RAST revealed predominance of Bacteroidetes, followed by
36 129 assembled metagenomes retrieved from MG-RAST for environmental GHs and identified 160,790 additi
37 amples integrating data and analyses from MG-RAST into popular third-party analysis tools or sequence
38 To show possible uses for the data from MG-RAST, we present several examples integrating data and a
40 e present an API that exposes the data in MG-RAST for consumption by our users, greatly enhancing the
41 ased analysis tools and infrastructure in MG-RAST provide limited capability for data retrieval and a
42 ata abstractions and indices available in MG-RAST; and use the results presented in-browser for explo
45 gh our experience with metagenomics-RAST (MG-RAST), the most popular metagenomics analysis pipeline.
48 agenomic datasets were analyzed using the MG-RAST metagenomic analysis server and STAMP v2.1.3 (Stati
52 rface) we have greatly expanded access to MG-RAST data, as well as provided a mechanism for the use o
60 RAST tool kit (RASTtk), a modular version of RAST that enables researchers to build custom annotation
64 s the current state of commercial phenotypic RAST including tests designed to report antimicrobial su
66 in reactions were associated with a positive RAST (14/23) as well as with specific IgE (13/23) and Ig
67 tides thereof were studied with quantitative RAST-based methods, in ELISA, basophil activation and Ig
68 ied by competitive radioallergosorbent test (RAST) and antibody-nanoarchitecture complexes by transmi
71 positive serum radioallergosorbent testing (RAST), nasal eosinophilia, or elevated nasal ECP (odds r
72 e activity coefficients, gammai, better than RAST combined with the Wilson equation or the Nonrandom
79 ectedness of the SEED database and RAST, the RAST annotation pipeline and updates to both resources.
81 ory (AST) and real adsorbed solution theory (RAST) either frequently show high prediction deviations
82 T (SIAST) and Real Adsorbed Solution Theory (RAST), to bisolute adsorption of organic compounds onto
83 which a new modeling strategy coupling FN to RAST and requiring only single-solute data was proposed.
85 han 10,000, are consistently annotated using RAST, the Rapid Annotations using Subsystems Technology.