knitr::opts_chunk$set( collapse = TRUE )
The purpose of this package is to make it easy to query the Human Cell Atlas Data Portal via their data browser API. Visit the Human Cell Atlas for more information on the project.
Evaluate the following code chunk to install packages required for this vignette.
## install from Bioconductor if you haven't already pkgs <- c("httr", "dplyr", "LoomExperiment", "hca") pkgs_needed <- pkgs[!pkgs %in% rownames(installed.packages())] BiocManager::install(pkgs_needed)
Load the packages into your R session.
library(httr) library(dplyr) library(LoomExperiment) library(hca)
To illustrate use of this package, consider the task of downloading a 'loom' file summarizing single-cell gene expression observed in an HCA research project. This could be accomplished by visiting the HCA data portal (at https://data.humancellatlas.org/explore) in a web browser and selecting projects interactively, but it is valuable to accomplish the same goal in a reproducible, flexible, programmatic way. We will (1) discover projects available in the HCA Data Coordinating Center that have loom files; and (2) retrieve the file from the HCA and import the data into R as a 'LoomExperiment' object. For illustration, we focus on the 'Single cell transcriptome analysis of human pancreas reveals transcriptional signatures of aging and somatic mutation patterns' project.
Use projects()
to retrieve the first 200 projects in the HCA's
default catalog.
projects(size = 200)
Use filters()
to restrict the projects to just those that contain at
least one 'loom' file.
project_filter <- filters(fileFormat = list(is = "loom")) project_tibble <- projects(project_filter) project_tibble
Use standard R commands to further filter projects to the one we are
interested in, with title starting with "Single...". Extract the
unique projectId
for the first project with this title.
project_tibble |> filter(startsWith(projectTitle, "Single")) |> head(1) |> t() projectIds <- project_tibble |> filter(startsWith(projectTitle, "Single")) |> dplyr::pull(projectId) projectId <- projectIds[1]
A project id can be used to discover the title or additional project information.
project_title(projectId) project_information(projectId)
files()
retrieves (the first 1000) files from the Human Cell Atlas
data portal. Construct a filter to restrict the files to loom files
from the project we are interested in.
file_filter <- filters( projectId = list(is = projectId), fileFormat = list(is = "loom") ) # only the two smallest files file_tibble <- files(file_filter, size = 2, sort = "fileSize", order = "asc") file_tibble
files_download()
will download one or more files (one for each row)
in file_tibble
. The download is more complicated than simply
following the url
column of file_tibble
, so it is not possible to
simply copy the url into a browser. We'll download the file and then
immediately import it into R.
file_locations <- file_tibble |> files_download() LoomExperiment::import(unname(file_locations[1]), type ="SingleCellLoomExperiment")
Note that files_download()
uses [BiocFileCache][https://bioconductor.org/packages/BiocFileCache],
so individual files are only downloaded once.
h5ad
filesThis example walks through the process of file discovery and retrieval
in a little more detail, using h5ad
files created by the Python
AnnData analysis software and available for some experiments in the
default catalog.
The first challenge is to understand what file formats are available from the HCA. Obtain a tibble describing the 'facets' of the data, the number of terms used in each facet, and the number of distinct values used to describe projects.
projects_facets()
Note the fileFormat
facet, and repeat projects_facets()
to
discover detail about available file formats
projects_facets("fileFormat")
Note that there are 8 uses of the h5ad
file format. Use this as a
filter to discover relevant projects.
filters <- filters(fileFormat = list(is = "h5ad")) projects(filters)
The default tibble produced by projects()
contains only some of the
information available; the information is much richer.
To obtain a tibble with an expanded set of columns, you can specify that using
the as
parameter set to "tibble_expanded"
.
# an expanded set of columns for all or the first 4 projects projects(as = 'tibble_expanded', size = 4)
In the next sections, we'll cover other options for the as
parameter, and the data formats
they return.
projects()
as an R list
Instead of retrieving the result of projects()
as a tibble, retrieve
it as a 'list-of-lists'
projects_list <- projects(size = 200, as = "list")
This is a complicated structure. We will use lengths()
, names()
,
and standard R list selection operations to navigate this a bit. At
the top level there are three elements.
lengths(projects_list)
hits
represents each project as a list, e.g,.
lengths(projects_list$hits[[1]])
shows that there are 10 different ways in which the first project is described. Each component is itself a list-of-lists, e.g.,
lengths(projects_list$hits[[1]]$projects[[1]]) projects_list$hits[[1]]$projects[[1]]$projectTitle
One can use standard R commands to navigate this data structure, and
to, e.g., extract the projectTitle
of each project.
projects()
as an lol
Use as = "lol"
to create a more convenient way to select, filter and
extract elements from the list-of-lists by projects()
.
lol <- projects(size = 200, as = "lol") lol
Use lol_select()
to restrict the lol
to particular paths, and
lol_filter()
to filter results to paths that are leafs, or with
specific numbers of entries.
lol_select(lol, "hits[*].projects[*]") lol_select(lol, "hits[*].projects[*]") |> lol_filter(n == 44, is_leaf)
lol_pull()
extracts a path from the lol
as a vector; lol_lpull()
extracts paths as lists.
titles <- lol_pull(lol, "hits[*].projects[*].projectTitle") length(titles) head(titles, 2)
projects()
tibbles with specific columnsThe path or its abbreviation can be used to specify the columns of
the tibble to be returned by the projects()
query.
Here we retrieve additional details of donor count and total cells by adding appropriate path abbreviations to a named character vector. Names on the character vector can be used to rename the path more concisely, but the paths must uniquely identify elements in the list-of-lists.
columns <- c( projectId = "hits[*].entryId", projectTitle = "hits[*].projects[*].projectTitle", genusSpecies = "hits[*].donorOrganisms[*].genusSpecies[*]", donorCount = "hits[*].donorOrganisms[*].donorCount", cellSuspensions.organ = "hits[*].cellSuspensions[*].organ[*]", totalCells = "hits[*].cellSuspensions[*].totalCells" ) projects <- projects(filters, columns = columns) projects
Note that the cellSuspensions.organ
and totalCells
columns have more than
one entry per project.
projects |> select(projectId, cellSuspensions.organ, totalCells)
In this case, the mapping between cellSuspensions.organ
and totalCells
is clear, but in general more refined navigation of the lol
structure may be
necessary.
projects |> select(projectId, cellSuspensions.organ, totalCells) |> filter( ## 2023-06-06 two projects have different 'organ' and ## 'totalCells' lengths, causing problems with `unnest()` lengths(cellSuspensions.organ) == lengths(totalCells) ) |> tidyr::unnest(c("cellSuspensions.organ", "totalCells"))
Select the following entry, augment the filter, and query available files
projects |> filter(startsWith(projectTitle, "Reconstruct")) |> glimpse()
This approach can be used to customize the tibbles returned by the
other main functions in the package, files()
, samples()
, and
bundles()
.
The relevant file can be selected and downloaded using the technique in the first example.
filters <- filters( projectId = list(is = "f83165c5-e2ea-4d15-a5cf-33f3550bffde"), fileFormat = list(is = "h5ad") ) files <- files(filters) |> head(1) # only first file, for demonstration files |> t()
file_path <- files_download(files)
"h5ad"
files can be read as SingleCellExperiment objects using the
zellkonverter package.
## don't want large amount of data read from disk sce <- zellkonverter::readH5AD(file_path, use_hdf5 = TRUE) sce
project_filter <- filters(fileFormat = list(is = "csv")) project_tibble <- projects(project_filter) project_tibble |> filter( startsWith( projectTitle, "Reconstructing the human first trimester" ) ) projectId <- project_tibble |> filter( startsWith( projectTitle, "Reconstructing the human first trimester" ) ) |> pull(projectId) file_filter <- filters( projectId = list(is = projectId), fileFormat = list(is = "csv") ) ## first 4 files will be returned file_tibble <- files(file_filter, size = 4) file_tibble |> files_download()
The files()
, bundles()
, and samples()
can all return many 1000's
of results. It is necessary to 'page' through these to see all of
them. We illustrate pagination with projects()
, retrieving only 30 projects.
Pagination works for the default tibble
output
page_1_tbl <- projects(size = 30) page_1_tbl page_2_tbl <- page_1_tbl |> hca_next() page_2_tbl ## should be identical to page_1_tbl page_2_tbl |> hca_prev()
Pagination also works for the lol
objects
page_1_lol <- projects(size = 5, as = "lol") page_1_lol |> lol_pull("hits[*].projects[*].projectTitle") page_2_lol <- page_1_lol |> hca_next() page_2_lol |> lol_pull("hits[*].projects[*].projectTitle") ## should be identical to page_1_lol page_2_lol |> hca_prev() |> lol_pull("hits[*].projects[*].projectTitle")
Much like projects()
and files()
, samples()
and bundles()
allow you to
provide a filter
object and additional criteria to retrieve data in the
form of samples and bundles respectively
heart_filters <- filters(organ = list(is = "heart")) heart_samples <- samples(filters = heart_filters, size = 4) heart_samples heart_bundles <- bundles(filters = heart_filters, size = 4) heart_bundles
HCA experiments are organized into catalogs, each of which can be summarized
with the hca::summary()
function
heart_filters <- filters(organ = list(is = "heart")) hca::summary(filters = heart_filters, type = "fileTypeSummaries") first_catalog <- catalogs()[1] hca::summary(type = "overview", catalog = first_catalog)
Each project, file, sample, and bundles has its own unique ID by which, in conjunction with its catalog, can be to uniquely identify them.
heart_filters <- filters(organ = list(is = "heart")) heart_projects <- projects(filters = heart_filters, size = 4) heart_projects projectId <- heart_projects |> filter( startsWith( projectTitle, "Cells of the adult human" ) ) |> dplyr::pull(projectId) result <- projects_detail(uuid = projectId)
The result is a list containing three elements representing
information for navigating next or previous (alphabetical, by default)
(pagination
) project, the filters (termFacets
) available, and
details of the project (hits
).
names(result)
As mentioned above, the hits
are a complicated list-of-lists
structure. A very convenient way to explore this structure visually
is with listview::jsonedit(result)
. Selecting individual elements is
possible using the lol
interface; an alternative is
cellxgenedp::jmespath()
.
lol(result)
See the accompanying "Human Cell Atlas Manifests" vignette on details
pertaining to the use of the manifest
endpoint and further
annotation of .loom
files.
sessionInfo()
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