loadL1K {slinky} | R Documentation

## loadL1K

### Description

Convert data from gctx file to SummarizedExperiment, pulling metadata from various sources. Specifying the subset of data you want can be done is various ways. The simplest example is with explicit subsetting (e.g. `data <- loadL1K(sl[1:978, 1:10])`, which is equivalent to `data <- as(sl[1:978, 1:10], "SummarizedExperiment")`). However, more sophisticated data loading can be achieved, for example by specifing a specific perturbagen (`pert`), or even an explicit `where_clause` which will be passed directly to the clue.io API. Thus, this function supports users with varying degrees of familiarity with the structure and content of the L1000 metadata. All arguments are optional.

### Usage

    loadL1K(x, ids = character(), pert = character(),
      cell_line = character(), type = NULL, where_clause = character(),
      gold = TRUE, inferred = TRUE, fields = character(),
      controls = FALSE, cl = NULL, verbose = FALSE)

    ## S4 method for signature 'Slinky'
    loadL1K(x, ids = character(), pert = character(),
      cell_line = character(), type = NULL, where_clause = character(),
      gold = FALSE, inferred = TRUE, fields = character(),
      controls = FALSE, cl = NULL, verbose = FALSE)

### Arguments

`x` | A slinky object
`ids` | distil_ids to include in the Expression Set.
`pert` | name (pert_iname) of perturbation for which data is desired. Supercedes value for `pert_iname` specified in `where_clause` (if any).
`cell_line` | name (cell_id) of cell line for which data is desired. Supercedes value for `cell_id` specified in `where_clause` (if any).
`type` | Optional type (pert_type) of perturbation for which data is desired, should be one of `c("trt_cp", "trt_sh", "trt_oe")` or NULL (default)
`where_clause` | Rather than specifying above terms, an explicit where_clause may be provided to identify the data to be loaded from the gctx file. This will be passed directly the the /pert endpoint of the clue.io API, and full documentation of the query options can be reviewed at the above link.
`gold` | Should we limit to instances classified as "gold" by the L1000 project (by virtue of their low inter-replicate variability)? Default is `TRUE`.
`inferred` | Should the inferred (non-landmark) genes be included in the analysis? Default is TRUE. Ignored if index is specified.
`fields` | Fields to include in the expression set's phenodata. Default is all available.
`controls` | Should same-plate controls be identified and included? Default is FALSE.
`cl` | Optional cluster object to speed up data retrieval from clue.io. Please use caution...a large cluster might produce requests to the API at an obnoxious rate.
`verbose` | Do you want to know how things are going? Default is FALSE

### Value

Object of type `SummarizedExperiment` containing expression and meta data. #' @name loadL1K

### Examples

    # for build/demo only.  You MUST use your own key when using the slinky
    # package.
    user_key <- httr::content(httr::GET('https://api.clue.io/temp_api_key'),
                              as='parsed')$user_key
    sl <- Slinky(user_key,
                     system.file('extdata', 'demo.gctx',
                          package='slinky'),
                     system.file('extdata', 'demo_inst_info.txt',
                         package = 'slinky'))
    amox_gold <- clueInstances(sl, where_clause = list("pert_type" = "trt_cp",
                                                      "pert_iname" = "amoxicillin",
                                                      "cell_id" = "MCF7",
                                                      "is_gold" = TRUE),
                              poscon = "omit")
    ids.ctrl <- controls(sl, ids = amox_gold)$distil_id
    amox_and_control <- loadL1K(sl, ids = c(amox_gold,
                                           ids.ctrl))
    str(SummarizedExperiment::assays(amox_and_control)[[1]])

[Package slinky version 1.8.0 Index]