spatialdecon: Mixed cell deconvolution of spatiall-resolved gene expression...

In Nanostring-Biostats/SpatialDecon: Deconvolution of mixed cells from spatial and/or bulk gene expression data

Mixed cell deconvolution of spatiall-resolved gene expression data

Description

Runs the spatialdecon algorithm with added optional functionalities. Workflow is:

1. compute weights from raw data

2. Estimate a tumor profile and merge it into the cell profiles matrix

3. run deconvolution once

4. remove poorly-fit genes from first round of decon

5. re-run decon with cleaned-up gene set

6. combine closely-related cell types

7. compute p-values

8. rescale abundance estimates, to proportions of total, proportions of immune, cell counts

Usage

spatialdecon(
  norm,
  bg,
  X = NULL,
  raw = NULL,
  wts = NULL,
  resid_thresh = 3,
  lower_thresh = 0.5,
  align_genes = TRUE,
  is_pure_tumor = NULL,
  n_tumor_clusters = 10,
  cell_counts = NULL,
  cellmerges = NULL,
  maxit = 1000
)

Arguments

norm	p-length expression vector or p * N expression matrix - the actual (linear-scale) data
bg	Same dimension as norm: the background expected at each data point.
X	Cell profile matrix. If NULL, the safeTME matrix is used.
raw	Optional for using an error model to weight the data points. p-length expression vector or p * N expression matrix - the raw (linear-scale) data
wts	Optional, a matrix of weights.
resid_thresh	A scalar, sets a threshold on how extreme individual data points' values can be (in log2 units) before getting flagged as outliers and set to NA.
lower_thresh	A scalar. Before log2-scale residuals are calculated, both observed and fitted values get thresholded up to this value. Prevents log2-scale residuals from becoming extreme in points near zero.
align_genes	Logical. If TRUE, then Y, X, bg, and wts are row-aligned by shared genes.
is_pure_tumor	A logical vector denoting whether each AOI consists of pure tumor. If specified, then the algorithm will derive a tumor expression profile and merge it with the immune profiles matrix.
n_tumor_clusters	Number of tumor-specific columns to merge into the cell profile matrix. Has an impact only when is_pure_tumor argument is used to indicate pure tumor AOIs. Takes this many clusters from the pure-tumor AOI data and gets the average expression profile in each cluster. Default 10.
cell_counts	Number of cells estimated to be within each sample. If provided alongside norm_factors, then the algorithm will additionally output cell abundance esimtates on the scale of cell counts.
cellmerges	A list object holding the mapping from beta's cell names to combined cell names. If left NULL, then defaults to a mapping of granular immune cell definitions to broader categories.
maxit	Maximum number of iterations. Default 1000.

Value

a list:

• beta: matrix of cell abundance estimates, cells in rows and observations in columns

• sigmas: covariance matrices of each observation's beta estimates

• p: matrix of p-values for H0: beta == 0

• t: matrix of t-statistics for H0: beta == 0

• se: matrix of standard errors of beta values

• prop_of_all: rescaling of beta to sum to 1 in each observation

• prop_of_nontumor: rescaling of beta to sum to 1 in each observation, excluding tumor abundance estimates

• cell.counts: beta rescaled to estimate cell numbers, based on prop_of_all and nuclei count

• beta.granular: cell abundances prior to combining closely-related cell types

• sigma.granular: sigmas prior to combining closely-related cell types

• cell.counts.granular: cell.counts prior to combining closely-related cell types

• resids: a matrix of residuals from the model fit. (log2(pmax(y, lower_thresh)) - log2(pmax(xb, lower_thresh))).

• X: the cell profile matrix used in the decon fit.

Examples

data(mini_geomx_dataset)
data(safeTME)
data(safeTME.matches)
# estimate background:
mini_geomx_dataset$bg <- derive_GeoMx_background(
  norm = mini_geomx_dataset$normalized,
  probepool = rep(1, nrow(mini_geomx_dataset$normalized)),
  negnames = "NegProbe"
)
# run basic decon:
res0 <- spatialdecon(
  norm = mini_geomx_dataset$normalized,
  bg = mini_geomx_dataset$bg,
  X = safeTME
)
# run decon with bells and whistles:
res <- spatialdecon(
  norm = mini_geomx_dataset$normalized,
  bg = mini_geomx_dataset$bg,
  X = safeTME,
  cellmerges = safeTME.matches,
  cell_counts = mini_geomx_dataset$annot$nuclei,
  is_pure_tumor = mini_geomx_dataset$annot$AOI.name == "Tumor"
)

Nanostring-Biostats/SpatialDecon documentation built on Jan. 26, 2024, 8:20 p.m.