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. 2019 Aug 10;36(3):782–788. doi: 10.1093/bioinformatics/btz619

Fig. 1.

Fig. 1.

Flow diagram for the MIND algorithm. (a) For a set of relevant cell types, select cell type marker genes and build a signature matrix using reference samples. (b) Multiple transcriptomes are measured from each subject; here, one transcriptome for each of multiple brain regions. (c) Using an existing deconvolution method, e.g. non-negative least squares, estimate the cell type fractions for each brain region and subject. Here we depict K = 4 cell types for which their fractions will be estimated per brain region. (d) With results from (b) and (c), MIND estimates cell-type-specific (CTS) expression for each of p genes for each subject and cell type. Colors map to the cell types in (c) and (d) and we depict two of n subjects, 1 and n. (e) Matrix representation of key data elements of the MIND algorithm: for each of T brain regions for subject i, expression of p genes from the transcriptome is measured, Xij; and the key outputs are the subject level CTS gene expression (Ai) and the subject and measurement level cell type fractions (Wi). (f) Examples of downstream applications for MIND. (Color version of this figure is available at Bioinformatics online.)