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PAN, Y.

Publications and source records attributed to PAN, Y..

3 recordsLinked to original sources

CREB: Consistent Reference External Batch Harmonization

AO_SCPLOWBSTRACTC_SCPLOWMachine learning models using functional magnetic resonance imaging (fMRI) are becoming increasingly popular - these models often rely on training data from multiple, large, and publicly available datasets. It is often necessary to harmonize these data across sites and sequences, and algorithms like ComBat are frequently applied to correct for these differences. This has been shown to improve model performance and generalizability. However, applying traditional ComBat necessitates harmonizing all data (train, validation, test, and other unseen external test sets) simultaneously, which leads to potential data leakage and limits application to new unseen data. We introduce Consistent Reference External Batch (CREB) harmonization, a novel extension of ComBat that learns the prior distribution of site effects exclusively from a designated training set. This learned prior serves as a consistent, easily deployable reference point that employs the empirical Bayes framework to update the site effect for any new, external unseen data. This approach enables training, validation, and test sets to be harmonized separately, thereby preventing data leakage, ensuring the integrity of downstream analyses, and application to new unseen data. CREB is different from traditional ComBat in which each sites prior distribution is estimated at once, but this cannot be applied to unseen data or data from sites not included in the original set of data. We tested CREB with train data from 2846 participants (ages 18-97 years) across 9 different studies and test data from 1113 participants (ages 18-88 years) from 3 studies. We evaluated the performance of harmonization with functional connectivity and gray matter volume. We show that CREB can effectively harmonize the test data to the train data, and have comparable performance to ComBat. CREB is able to conduct this harmonization in a two-step procedure that prevents leakage and is deployable to new unseen data. Finally, we tested whether CREB could similarly preserve biological variance (e.g., whether age associations were preserved after harmonization). We found that CREB, like ComBat could preserve age associations with both functional connectivity and gray matter volume measures. CREB provides an easily deployable, robust harmonization method to standardize data to a common reference distribution, making it uniquely suitable for training generalizable machine learning models.

bioengineering↗

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

bioinformatics↗

Collaborative Cross Mouse Populations as a Resource for the Study of Epilepsy

Epilepsy is a neurological disorder with complex etiologies and genetic architecture. Animal models have a critical role in understanding the pathophysiology of epilepsy. Here we studied epilepsy utilizing a genetic reference population of Collaborative Cross (CC) mice with publicly available whole genome sequences. We measured multiple epilepsy traits in 35 CC strains, and we identified novel animal models that exhibit extreme outcomes in seizure susceptibility, seizure propagation, epileptogenesis, and sudden unexpected death in epilepsy. We performed QTL mapping in an F2 population and identified seven novel and one previously identified loci associated with seizure sensitivity. We combined whole genome sequence and hippocampal gene expression to pinpoint biologically plausible candidate genes and candidate variants associated with seizure sensitivity. These resources provide a powerful toolbox for studying complex features of seizures and for identifying genes associated with particular seizure outcomes, and hence will facilitate the development of new therapeutic targets for epilepsy.

neuroscience↗