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Skalic, M.

Publications and source records attributed to Skalic, M..

2 recordsLinked to original sources

In silico PK predictions in Drug Discovery: Benchmarking of Strategies to Integrate Machine Learning with Empiric and Mechanistic PK modelling

A successful drug needs to combine several properties including high potency and good pharmacokinetic (PK) properties to sustain efficacious plasma concentration over time. To estimate required doses for preclinical animal efficacy models or for the clinics, in vivo PK studies need to be conducted. While the prediction of ADME properties of compounds using Machine Learning (ML) models based on chemical structures is well established in drug discovery, the prediction of complete plasma concentration-time profiles has only recently gained attention. In this study, we systematically compare various approaches that integrate ML models with mechanistic PK models to predict PK profiles in rats after i.v. administration prior to synthesis. More specifically, we compare a standard noncompartmental analysis (NCA) based approach (prediction of CL and Vss), a pure ML approach (non-mechanistic PK description), a compartmental modeling approach, and a physiologically based pharmacokinetic (PBPK) approach. Our study based on internal preclinical data shows that the latter three approaches yield PK profile predictions of comparable accuracy (evaluated as geometric mean fold errors for each profile) across a large test set (>1000 small molecules). In summary, we demonstrate the improved ability to prioritize drug candidates with desirable PK properties prior to synthesis with ML predictions.

bioinformatics↗

Fast and accurate differential splicing analysis across multiple conditions with replicates

Multiple approaches have been proposed to study differential splicing from RNA sequencing (RNA-seq) data1, including the analysis of transcript isoforms2,3, clusters of splice-junctions4,5, alternative splicing events6-8 and exonic regions9. However, many challenges remain unsolved, including the limitation in speed, the computing capacity and storage requirements, the constraints in the number of reads needed to achieve sufficient accuracy, and the lack of robust methods to account for variability between replicates and for analyses across multiple conditions. We present here a significant extension of SUPPA8 to enable streamlined analysis of differential splicing across multiple conditions, taking into account biological variability. We show that SUPPA differential splicing analysis achieves high accuracy using extensive experimental and simulated data compared to other methods; and shows higher accuracy at low sequencing depth, with short read lengths, and using replicas with unbalanced depth, which has important implications for the cost-effective use of RNA-seq data for splicing analysis. We also validate the analysis of multiple conditions with SUPPA by studying differential splicing during iPS-cell to neuron differentiation and during erythroblast differentiation, providing support for the applicability of SUPPA for the robust analysis of differential splicing beyond binary comparisons.

bioinformatics↗