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added vanA to vanE positive Enterococci
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NEWS.md
2
NEWS.md
@ -23,7 +23,7 @@
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* Introduction to AMR as a vignette
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#### Changed
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* Added 226 microorganisms to the `microorganisms` data set and removed the few viruses it contained, now *n* = 2,664 (2,225 bacteria, 285 fungi/yeasts, 153 parasites, 1 other)
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* Added 231 microorganisms to the `microorganisms` data set and removed the few viruses it contained, now *n* = 2,669 (2,230 bacteria, 285 fungi/yeasts, 153 parasites, 1 other)
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* Added three antimicrobial agents to the `antibiotics` data set: Terbinafine (D01BA02), Rifaximin (A07AA11) and Isoconazole (D01AC05)
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* Added 163 trade names to the `antibiotics` data set, it now contains 298 different trade names in total, e.g.:
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```r
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6
R/data.R
6
R/data.R
@ -122,8 +122,8 @@
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#' Data set with human pathogenic microorganisms
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#'
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#' A data set containing 2,664 (potential) human pathogenic microorganisms. MO codes can be looked up using \code{\link{guess_mo}}.
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#' @format A \code{\link{tibble}} with 2,664 observations and 16 variables:
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#' A data set containing 2,669 (potential) human pathogenic microorganisms. MO codes can be looked up using \code{\link{guess_mo}}.
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#' @format A \code{\link{tibble}} with 2,669 observations and 16 variables:
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#' \describe{
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#' \item{\code{mo}}{ID of microorganism}
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#' \item{\code{bactsys}}{Bactsyscode of microorganism}
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@ -158,7 +158,7 @@
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#' Translation table for UMCG with ~1,100 microorganisms
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#'
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#' A data set containing all bacteria codes of UMCG MMB. These codes can be joined to data with an ID from \code{\link{microorganisms}$mo} (using \code{\link{left_join_microorganisms}}). GLIMS codes can also be translated to valid \code{MO}s with \code{\link{guess_mo}}.
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#' @format A \code{\link{tibble}} with 1,090 observations and 2 variables:
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#' @format A \code{\link{tibble}} with 1,095 observations and 2 variables:
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#' \describe{
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#' \item{\code{umcg}}{Code of microorganism according to UMCG MMB}
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#' \item{\code{mo}}{Code of microorganism in \code{\link{microorganisms}}}
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@ -44,7 +44,7 @@ This `AMR` package basically does four important things:
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1. It **cleanses existing data**, by transforming it to reproducible and profound *classes*, making the most efficient use of R. These functions all use artificial intelligence to guess results that you would expect:
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* Use `as.mo` to get an ID of a microorganism. The IDs are quite obvious - the ID of *E. coli* is "ESCCOL" and the ID of *S. aureus* is "STAAUR". The function takes almost any text as input that looks like the name or code of a microorganism like "E. coli", "esco" and "esccol". Even `as.mo("MRSA")` will return the ID of *S. aureus*. Moreover, it can group all coagulase negative and positive *Staphylococci*, and can transform *Streptococci* into Lancefield groups. To find bacteria based on your input, this package contains a freely available database of ~2,650 different (potential) human pathogenic microorganisms.
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* Use `as.mo` to get an ID of a microorganism. The IDs are quite obvious - the ID of *E. coli* is "ESCCOL" and the ID of *S. aureus* is "STAAUR". The function takes almost any text as input that looks like the name or code of a microorganism like "E. coli", "esco" and "esccol". Even `as.mo("MRSA")` will return the ID of *S. aureus*. Moreover, it can group all coagulase negative and positive *Staphylococci*, and can transform *Streptococci* into Lancefield groups. To find bacteria based on your input, this package contains a freely available database of almost 3,000 different (potential) human pathogenic microorganisms.
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* Use `as.rsi` to transform values to valid antimicrobial results. It produces just S, I or R based on your input and warns about invalid values. Even values like "<=0.002; S" (combined MIC/RSI) will result in "S".
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* Use `as.mic` to cleanse your MIC values. It produces a so-called factor (called *ordinal* in SPSS) with valid MIC values as levels. A value like "<=0.002; S" (combined MIC/RSI) will result in "<=0.002".
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* Use `as.atc` to get the ATC code of an antibiotic as defined by the WHO. This package contains a database with most LIS codes, official names, DDDs and even trade names of antibiotics. For example, the values "Furabid", "Furadantin", "nitro" all return the ATC code of Nitrofurantoine.
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\name{microorganisms}
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\alias{microorganisms}
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\title{Data set with human pathogenic microorganisms}
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\format{A \code{\link{tibble}} with 2,664 observations and 16 variables:
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\format{A \code{\link{tibble}} with 2,669 observations and 16 variables:
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\describe{
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\item{\code{mo}}{ID of microorganism}
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\item{\code{bactsys}}{Bactsyscode of microorganism}
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@ -27,7 +27,7 @@
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microorganisms
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}
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\description{
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A data set containing 2,664 (potential) human pathogenic microorganisms. MO codes can be looked up using \code{\link{guess_mo}}.
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A data set containing 2,669 (potential) human pathogenic microorganisms. MO codes can be looked up using \code{\link{guess_mo}}.
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}
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\seealso{
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\code{\link{guess_mo}} \code{\link{antibiotics}} \code{\link{microorganisms.umcg}}
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\name{microorganisms.umcg}
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\alias{microorganisms.umcg}
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\title{Translation table for UMCG with ~1,100 microorganisms}
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\format{A \code{\link{tibble}} with 1,090 observations and 2 variables:
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\format{A \code{\link{tibble}} with 1,095 observations and 2 variables:
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\describe{
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\item{\code{umcg}}{Code of microorganism according to UMCG MMB}
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\item{\code{mo}}{Code of microorganism in \code{\link{microorganisms}}}
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1. It **cleanses existing data**, by transforming it to reproducible and profound *classes*, making the most efficient use of R. These functions all use artificial intelligence to guess results that you would expect:
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* Use `as.mo` to get an ID of a microorganism. The IDs are quite obvious - the ID of *E. coli* is "ESCCOL" and the ID of *S. aureus* is "STAAUR". The function takes almost any text as input that looks like the name or code of a microorganism like "E. coli", "esco" and "esccol". Even `as.mo("MRSA")` will return the ID of *S. aureus*. Moreover, it can group all coagulase negative and positive *Staphylococci*, and can transform *Streptococci* into Lancefield groups. To find bacteria based on your input, this package contains a freely available database of ~2,650 different (potential) human pathogenic microorganisms.
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* Use `as.mo` to get an ID of a microorganism. The IDs are quite obvious - the ID of *E. coli* is "ESCCOL" and the ID of *S. aureus* is "STAAUR". The function takes almost any text as input that looks like the name or code of a microorganism like "E. coli", "esco" and "esccol". Even `as.mo("MRSA")` will return the ID of *S. aureus*. Moreover, it can group all coagulase negative and positive *Staphylococci*, and can transform *Streptococci* into Lancefield groups. To find bacteria based on your input, this package contains a freely available database of almost 3,000 different (potential) human pathogenic microorganisms.
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* Use `as.rsi` to transform values to valid antimicrobial results. It produces just S, I or R based on your input and warns about invalid values. Even values like "<=0.002; S" (combined MIC/RSI) will result in "S".
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* Use `as.mic` to cleanse your MIC values. It produces a so-called factor (called *ordinal* in SPSS) with valid MIC values as levels. A value like "<=0.002; S" (combined MIC/RSI) will result in "<=0.002".
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* Use `as.atc` to get the ATC code of an antibiotic as defined by the WHO. This package contains a database with most LIS codes, official names, DDDs and even trade names of antibiotics. For example, the values "Furabid", "Furadantin", "nitro" all return the ATC code of Nitrofurantoine.
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