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Lysenkova Wiklander, M.

Publications and source records attributed to Lysenkova Wiklander, M..

2 recordsLinked to original sources

Error reduction in leukemia machine learning classification with conformal prediction

PurposeRecent advances in machine learning (ML) have led to the development of classifiers that predict molecular subtypes of acute lymphoblastic leukemia (ALL) using RNA sequencing (RNA-seq) data. While these models have shown promising results, they often lack robust performance guarantees. The aim of this study was three-fold: to quantify the uncertainty of these classifiers; to provide prediction sets that control the false negative rate (FNR); and to perform implicit reduction by transforming incorrect predictions into uncertain predictions. MethodsConformal prediction is a distribution-agnostic framework for generating statistically calibrated prediction sets whose size reflects model uncertainty. In this study, we applied an extension called conformal risk control to ALLIUM, an RNA-seq ALL subtype classifier. Leveraging RNA-seq data from 1042 patient samples taken at diagnosis, we developed a multi-class conformal predictor, ALLCoP, which generates statistically guaranteed FNR-controlled prediction sets. ResultsALLCoP was able to create prediction sets with specified FNR tolerances ranging from 7.5-30%. In a validation cohort, ALLCoP successfully reduced the FNR of the ALLIUM classifier from 8.95% to 3.5%. For cases whose subtype was not previously known, the use of ALLCoP was able to reduce the occurrence of empty predictions from 37% to 17%. Notably, up to 34% of the multiple-class prediction sets included the PAX5alt subtype, suggesting that increased prediction set size may reflect secondary aberrations and biological complexity, contributing to classifier uncertainty. Finally, ALLCoP was validated on two additional RNA-seq ALL subtype classifiers, ALLSorts and ALLCatchR. ConclusionOur results highlight the potential of conformal prediction in enhancing the use of oncological RNA-seq subtyping classifiers and also in uncovering additional molecular aberrations of potential clinical importance.

bioinformatics↗

A complete digital karyotype of the B-cell leukemia REH cell line resolved by long-read sequencing

The B-cell acute lymphoblastic leukemia (ALL) cell line REH, with the t(12;21) ETV6-RUNX1 translocation, is known to have a complex karyotype defined by a series of large-scale chromosomal rearrangements. Taken from a 15-year-old at relapse, the cell line offers a practical model for the study of high-risk pediatric B-ALL patients. In recent years, short-read DNA and RNA sequencing have emerged as a complement to analog karyotyping techniques in the resolution of structural variants in an oncological context. However, it is challenging to create a comprehensive digital karyotype of a genome with these techniques alone. Here, we explore the integration of long-read PacBio and Oxford Nanopore whole genome sequencing (WGS), IsoSeq RNA-sequencing, and short-read sequencing to create a detailed digital karyotype of the REH cell line. WGS refined the breakpoints of known aberrations and clarified the molecular traits of disrupted ALL-associated genes BTG1 and TBL1XR1, as well as the glucocorticoid receptor NR3C1. Several previously underreported structural variants were also uncovered, including deletions affecting the ALL-associated genes VPREB1 and NFATC1. Meanwhile, transcriptome sequencing identified seven fusion genes within the genomic breakpoints. Together, our extensive whole-genome investigation makes high-quality open-source data available to the leukemia genomics community. KEY POINTSO_LIA complete digital karyotype of the REH cell line was produced with short- and long-read DNA and RNA sequencing technologies. C_LIO_LIThe study enabled precise identification of structural variants, and the fusion genes expressed as the result of these variants. C_LI

cancer biology↗