Closed jashapiro closed 2 years ago
As long as we are adding options, we might want to add --soloMultiMappers EM
to use a similar quantification strategy as alevin-fry with EM... adding this adds a new quant matrix, so there is no loss of the original data.
closed by #160
The current version of the STARsolo mapping process at https://github.com/AlexsLemonade/alsf-scpca/blob/main/workflows/genetic-demux/map-sc-star.nf does not properly handle single nucleus data, which we do have for some multiplexed samples.
While I do not think this affects the BAM output, which is the main function we are using, it can affect the quantification, and the UMI/cell counts that are used for identifying and filtering cells. If we want to use STARsolo in the future for quantification, we would want it as well.
This should be a matter of checking the metadata for each sample and adding
--soloFeatures GeneFull
to include unspliced RNA in quantification.