Biologically Informative NA Deconvolution (BIND) excavates hidden features of the proteome from missing values in large-scale datasets
The fast-advancing mass spectrometry and related technologies have greatly extended the depth of coverage in large-scale proteomics studies, including single-cell applications. As sample numbers grow rapidly, it is often challenging to interpret the proteins with missing values that are often presented as "NA" (not available). It could be the evidence of no expression, low expression below the detection threshold, or false negative detection due to technical issues. Existing methods for missing values imputation, while generally useful, rarely consider the non-random NA values that inform biological significance. In the current study, we developed Biologically Informative NA Deconvolution (BIND) that applies an adaptive neighborhood-based modeling to deconvolve the nature of NAs as "biological" (low/no expression) or technical (experimental errors). Applying to multiple cell line datasets and human tissue extracellular vesicle datasets, BIND excavated the NAs that indicated "hallmark absence" of unique proteins. This led to improvements in protein-protein interaction analysis and the identification of novel disease biomarkers. To facilitate its public accessibility, we compiled BIND into a web server that features functional online operations and interactive visualizations. Furthermore, we demonstrated that the BIND server could deconvolve the NAs and improve the analyses of single-cell proteomics datasets. Overall, BIND delineates the biological significance of missing values rather than treating them as a burden, providing a critical perspective for understanding the complex proteome in various biological contexts. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=144 SRC="FIGDIR/small/660508v1_ufig1.gif" ALT="Figure 1"> View larger version (52K): org.highwire.dtl.DTLVardef@1a9d7c4org.highwire.dtl.DTLVardef@194b2d9org.highwire.dtl.DTLVardef@169d3bborg.highwire.dtl.DTLVardef@cba0de_HPS_FORMAT_FIGEXP M_FIG C_FIG