as_tibble() turns an existing object, such as a data frame or matrix, into a so-called tibble, a data frame with class tbl_df. This is in contrast with tibble(), which builds a tibble from individual columns. as_tibble() is to tibble() as base::as.data.frame() is to base::data.frame().

as_tibble() is an S3 generic, with methods for:

as_tibble_row() converts a vector to a tibble with one row. If the input is a list, all elements must have size one.

as_tibble_col() converts a vector to a tibble with one column.

# S3 method for class 'SpatialExperiment'
as_tibble(
  x,
  ...,
  .name_repair = c("check_unique", "unique", "universal", "minimal"),
  rownames = pkgconfig::get_config("tibble::rownames", NULL)
)

Arguments

x

A data frame, list, matrix, or other object that could reasonably be coerced to a tibble.

...

Unused, for extensibility.

.name_repair

Treatment of problematic column names:

  • "minimal": No name repair or checks, beyond basic existence,

  • "unique": Make sure names are unique and not empty,

  • "check_unique": (default value), no name repair, but check they are unique,

  • "universal": Make the names unique and syntactic

  • a function: apply custom name repair (e.g., .name_repair = make.names for names in the style of base R).

  • A purrr-style anonymous function, see rlang::as_function()

This argument is passed on as repair to vctrs::vec_as_names(). See there for more details on these terms and the strategies used to enforce them.

rownames

How to treat existing row names of a data frame or matrix:

  • NULL: remove row names. This is the default.

  • NA: keep row names.

  • A string: the name of a new column. Existing rownames are transferred into this column and the row.names attribute is deleted. No name repair is applied to the new column name, even if x already contains a column of that name. Use as_tibble(rownames_to_column(...)) to safeguard against this case.

Read more in rownames.

Value

tibble

Row names

The default behavior is to silently remove row names.

New code should explicitly convert row names to a new column using the rownames argument.

For existing code that relies on the retention of row names, call pkgconfig::set_config("tibble::rownames" = NA) in your script or in your package's .onLoad() function.

Life cycle

Using as_tibble() for vectors is superseded as of version 3.0.0, prefer the more expressive as_tibble_row() and as_tibble_col() variants for new code.

See also

tibble() constructs a tibble from individual columns. enframe() converts a named vector to a tibble with a column of names and column of values. Name repair is implemented using vctrs::vec_as_names().

Examples

example(read10xVisium)
#> 
#> rd10xV> dir <- system.file(
#> rd10xV+   file.path("extdata", "10xVisium"), 
#> rd10xV+   package = "SpatialExperiment")
#> 
#> rd10xV> sample_ids <- c("section1", "section2")
#> 
#> rd10xV> samples <- file.path(dir, sample_ids, "outs")
#> 
#> rd10xV> list.files(samples[1])
#> [1] "raw_feature_bc_matrix" "spatial"              
#> 
#> rd10xV> list.files(file.path(samples[1], "spatial"))
#> [1] "scalefactors_json.json"    "tissue_lowres_image.png"  
#> [3] "tissue_positions_list.csv"
#> 
#> rd10xV> file.path(samples[1], "raw_feature_bc_matrix")
#> [1] "/__w/_temp/Library/SpatialExperiment/extdata/10xVisium/section1/outs/raw_feature_bc_matrix"
#> 
#> rd10xV> (spe <- read10xVisium(samples, sample_ids, 
#> rd10xV+   type = "sparse", data = "raw", 
#> rd10xV+   images = "lowres", load = FALSE))
#> # A SpatialExperiment-tibble abstraction: 99 × 7
#> # Features = 50 | Cells = 99 | Assays = counts
#>    .cell              in_tissue array_row array_col sample_id pxl_col_in_fullres
#>    <chr>              <lgl>         <int>     <int> <chr>                  <int>
#>  1 AAACAACGAATAGTTC-1 FALSE             0        16 section1                2312
#>  2 AAACAAGTATCTCCCA-1 TRUE             50       102 section1                8230
#>  3 AAACAATCTACTAGCA-1 TRUE              3        43 section1                4170
#>  4 AAACACCAATAACTGC-1 TRUE             59        19 section1                2519
#>  5 AAACAGAGCGACTCCT-1 TRUE             14        94 section1                7679
#>  6 AAACAGCTTTCAGAAG-1 FALSE            43         9 section1                1831
#>  7 AAACAGGGTCTATATT-1 FALSE            47        13 section1                2106
#>  8 AAACAGTGTTCCTGGG-1 FALSE            73        43 section1                4170
#>  9 AAACATGGTGAGAGGA-1 FALSE            62         0 section1                1212
#> 10 AAACATTTCCCGGATT-1 FALSE            61        97 section1                7886
#> # ℹ 89 more rows
#> # ℹ 1 more variable: pxl_row_in_fullres <int>
#> 
#> rd10xV> # base directory 'outs/' from Space Ranger can also be omitted
#> rd10xV> samples2 <- file.path(dir, sample_ids)
#> 
#> rd10xV> (spe2 <- read10xVisium(samples2, sample_ids, 
#> rd10xV+   type = "sparse", data = "raw", 
#> rd10xV+   images = "lowres", load = FALSE))
#> # A SpatialExperiment-tibble abstraction: 99 × 7
#> # Features = 50 | Cells = 99 | Assays = counts
#>    .cell              in_tissue array_row array_col sample_id pxl_col_in_fullres
#>    <chr>              <lgl>         <int>     <int> <chr>                  <int>
#>  1 AAACAACGAATAGTTC-1 FALSE             0        16 section1                2312
#>  2 AAACAAGTATCTCCCA-1 TRUE             50       102 section1                8230
#>  3 AAACAATCTACTAGCA-1 TRUE              3        43 section1                4170
#>  4 AAACACCAATAACTGC-1 TRUE             59        19 section1                2519
#>  5 AAACAGAGCGACTCCT-1 TRUE             14        94 section1                7679
#>  6 AAACAGCTTTCAGAAG-1 FALSE            43         9 section1                1831
#>  7 AAACAGGGTCTATATT-1 FALSE            47        13 section1                2106
#>  8 AAACAGTGTTCCTGGG-1 FALSE            73        43 section1                4170
#>  9 AAACATGGTGAGAGGA-1 FALSE            62         0 section1                1212
#> 10 AAACATTTCCCGGATT-1 FALSE            61        97 section1                7886
#> # ℹ 89 more rows
#> # ℹ 1 more variable: pxl_row_in_fullres <int>
#> 
#> rd10xV> # tabulate number of spots mapped to tissue
#> rd10xV> cd <- colData(spe)
#> 
#> rd10xV> table(
#> rd10xV+   in_tissue = cd$in_tissue, 
#> rd10xV+   sample_id = cd$sample_id)
#>          sample_id
#> in_tissue section1 section2
#>     FALSE       28       27
#>     TRUE        22       22
#> 
#> rd10xV> # view available images
#> rd10xV> imgData(spe)
#> DataFrame with 2 rows and 4 columns
#>     sample_id    image_id   data scaleFactor
#>   <character> <character> <list>   <numeric>
#> 1    section1      lowres   ####   0.0510334
#> 2    section2      lowres   ####   0.0510334
spe |>
    as_tibble()
#> # A tibble: 99 × 7
#>    .cell              in_tissue array_row array_col sample_id pxl_col_in_fullres
#>    <chr>              <lgl>         <int>     <int> <chr>                  <int>
#>  1 AAACAACGAATAGTTC-1 FALSE             0        16 section1                2312
#>  2 AAACAAGTATCTCCCA-1 TRUE             50       102 section1                8230
#>  3 AAACAATCTACTAGCA-1 TRUE              3        43 section1                4170
#>  4 AAACACCAATAACTGC-1 TRUE             59        19 section1                2519
#>  5 AAACAGAGCGACTCCT-1 TRUE             14        94 section1                7679
#>  6 AAACAGCTTTCAGAAG-1 FALSE            43         9 section1                1831
#>  7 AAACAGGGTCTATATT-1 FALSE            47        13 section1                2106
#>  8 AAACAGTGTTCCTGGG-1 FALSE            73        43 section1                4170
#>  9 AAACATGGTGAGAGGA-1 FALSE            62         0 section1                1212
#> 10 AAACATTTCCCGGATT-1 FALSE            61        97 section1                7886
#> # ℹ 89 more rows
#> # ℹ 1 more variable: pxl_row_in_fullres <int>