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Hage, J.

Publications and source records attributed to Hage, J..

2 recordsLinked to original sources

Inferring absolute counts from proportions by constraining multivariate normal distributions

Biological measurements often result in proportional data, which derive from underlying biological counts. Proportion data are lacking a dimension of information as compared to counts, restricting available analysis methods and separating the data from the biology. We demonstrate a mathematical technique that estimates absolute counts corresponding to proportion data, which we refer to as Mahalanobis Count Inference (MCI). MCI uses information from a population-representative multivariate normal (MVN) distribution of component counts and ultimately outputs an estimated count and a confidence interval per observation proportion vector. We apply MCI to the imputation of white blood cell (WBC) counts, and of total mRNA within single cells. The method performs very well on total mRNA recapitulation (log-space Pearsons R = 0.81), and well enough on WBC counts to outperform proportions at multiple classification tasks. MCI operates with minimal assumptions, and is applicable to many compositional omics.

systems biology↗

Continuous DNA Methylation Deconvolution-Based Surrogate for B-Cell Differentiation State in CLL

Chronic Lymphocytic Leukemia (CLL) is clinically divided into IGHV mutated (M-CLL) and IGHV unmutated (U-CLL) subtypes, which are thought to arise from distinct cells of origin along the B-cell differentiation pathway. We measured genome-scale DNA methylation in purified CLL samples (n = 89) and utilized reference-based cell deconvolution techniques to develop a continuous metric of epigenetic similarity across a B-naive-like to B-memory-like scale (B-Index). B-Index accurately classifies CLL into clinical subtypes (98.8%), has a stronger epigenetic signal than IGHV gene percent identity, and demonstrates additional epigenetic signal within the M-CLL subgroup. We demonstrate that U-CLL is epigenetically more similar to B-memory than B-naive cells and reconcile previous reports of a B-naive-like epigenetic signal. The B-memory-like program of U-CLL is enriched for binding sites of transcription factors related to the germinal center activation pathway. Our findings provide epigenetic evidence for discerning CLL mechanisms of initiation and cell of origin. We also identified an epigenetic signal associated with tumor burden, which may have some relation to viral infections such as Epstein-Barr-Virus. Our cell-type deconvolution-based approach to developing a continuous metric for CLL epigenetic differentiation state can be applied to other tumors with multiple subtypes across differentiation stages.

cancer biology↗