The SpatialDecon library implements the SpatialDecon algorithm for mixed cell deconvolution in spatial gene expression datasets. (This algorithm also works in bulk expression profiling data.)
I received raw counts and normalized GeoMX data. The raw counts data contain multiple negative probes (negprobe-WTX). Do I need to compute the geometric mean of these negative probes in the raw counts data before using it in SpatialDecon? If so, please confirm whether I should calculate the geometric mean per column. Alternatively, may I exclude the negative probes from the raw counts and exclude the negprobe-WTX from the normalized data after computing per.observation.mean.neg and background matrix bg using the normalized data?
I received raw counts and normalized GeoMX data. The raw counts data contain multiple negative probes (negprobe-WTX). Do I need to compute the geometric mean of these negative probes in the raw counts data before using it in SpatialDecon? If so, please confirm whether I should calculate the geometric mean per column. Alternatively, may I exclude the negative probes from the raw counts and exclude the negprobe-WTX from the normalized data after computing per.observation.mean.neg and background matrix bg using the normalized data?