Search bioRxiv⌕ Search
Home/Archive/bioRxiv

bioRxiv · 10.1101/2023.11.11.566680

scLongTree: an accurate computational tool to infer the longitudinal tree for scDNAseq data

Khan, R.·Mallory, X.
View original source ↗Export metadata ↓

Abstract

Longitudinal single-cell DNA sequencing (scDNA-seq) refers to single-cell data sequenced at different time points providing more knowledge of the order of mutations than scDNA-seq taken at only one time point. The technique can facilitate the inference of subclonal trees that depict the evolution of cancer cells and facilitate understanding of how cancer grows, with implications for prognosis and treatment. There is currently a scarcity of tools that can infer subclonal trees based on longitudinal scDNA-seq, and existing tools are limited in accuracy and scale. We therefore introduce scLongTree, a computational tool that can accurately infer a subclonal tree based on longitudinal scDNA-seq. ScLongTree is scalable to hundreds of mutations, and outperforms state-of-the-art tools such as LACE, SCITE, and SiCloneFit on a comprehensive simulated dataset. Tests on a real dataset, SA501, showed that scLongTree can more accurately interpret the progressive growth of the tumor than LACE, and is more robust to different numbers of mutations being used. Tests on a large AML dataset AML107, which has 4,617 cells, show that scLongTree is scalable to thousands of cells. ScLongTree is freely available on https://github.com/compbio-mallory/sc_longitudinal_infer. Key pointsO_LIWe propose scLongTree that can infer the subclonal longitudinal tree for cancer given single-cell DNA sequencing data, and thus can facilitate the study of cancer evolution given the dataset from multiple time points. C_LIO_LIMultiple simulated data show that scLongTree is more accurate than existing state-of-the-art methods such as LACE, SCITE and SiCloneFit. C_LIO_LIScLongTree has been shown to have a higher scalability than LACE and thus can be applicable to the datasets that have hundreds of mutations. C_LIO_LIThe experiment on a real SA501 shows that scLongTree is more robust to the number of mutations than LACE. It consistently generates the same longitudinal tree even under different sets of mutations. C_LIO_LIThe experiment on AML107 shows that scLongTree is scalable to thousands of cells. C_LI

Explore related subjects

bioinformaticsPreprint

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Khan, R., Mallory, X.. 2023-11-15. scLongTree: an accurate computational tool to infer the longitudinal tree for scDNAseq data. https://doi.org/10.1101/2023.11.11.566680

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

bioRxiv2026

Accounting for pseudo-replication of Linkage Disequilibrium for contemporary Ne estimation

The Linkage Disequilibrium (LD) of unlinked loci can be used to estimate contemporary effective population size (Ne) of one to a few generations ago. In genomic datasets loci on different chromosomes are considered unlinked, but there are many more pairs of unlinked loci than there are independent pairs of chromosomes, resulting to confidence intervals (C.I.) being too narrow if the non-independence is not taken into account. Simulations were run to investigate the correlation structure among LD of unlinked loci, which can be expressed by the LD of loci along the same chromosomes, based on a discovery of a novel Random Probe LD estimator. We classify the correlation into two categories: overlapping of loci and disjoint pairs. The former is induced from the same locus being considered twice and is the stronger form of correlation. These correlations feed into {rho}, a parameter to quantify the degree of pseudo-replication in a dataset, and further a correction formula from which C.I. can be properly inferred. We demonstrate the use of our method via an analysis of genomic data from the malaria-transmitting Anopheles gambiae s.s mosquitoes. Apart from the point and C.I. estimates, we find that Var((r^2 ) ) is inflated by about 550 times due to pseudo-replication, highlighting the danger of not handling genetic correlation properly.

bioinformatics↗
bioRxiv2026

Accurate and scalable decontamination of imaging-based spatial transcriptomics via optimal transport

Imaging-based spatial transcriptomics enables molecule-resolved profiling of gene expression and tissue organization in situ. However, segmentation errors, transcript spillover and three-dimensional cell overlap can introduce misassigned transcripts into cell-level expression profiles, compromising biological interpretation and obscuring genuine signals. Existing methods either remove suspect expression at the cost of signal loss or lack a biologically grounded criterion for transcript assignment. Here we present CellDot, an optimal-transport framework that determines the fate of each transcript by retaining it in its host cell, reassigning it to a plausible neighboring cell or removing it as background. By integrating reference-guided expression compatibility with spatial information and data-adaptive constraints, CellDot enables accurate and traceable molecule-level correction while preserving biologically meaningful variation. In evaluations across multiple human tumor datasets, CellDot exhibited superior performance compared to existing decontamination methods, successfully restoring spatial expression patterns that matched independent cross-platform measurements. Moreover, it significantly enhanced the recovery of cellular states, intercellular communication, and spatial niche programs. Our experiments using real data demonstrated CellDot's scalability and established it as the only method applicable to a whole-transcriptome Atera dataset, underscoring its distinct advantages in the field of spatial transcriptomics.

bioinformatics↗
bioRxiv2026

Interpretable Machine Learning Reveals Complementary Age-Related Signatures in the Oral and Gut Microbiome

Whether combining microbiome data from multiple body sites improves prediction, and whether different sites carry complementary or redundant information, are distinct questions that most studies conflate into a single accuracy metric. This work makes two contributions, one methodological and one biological, using paired stool and oral cavity microbiome samples from 44 subjects across two age groups, healthy adults and newborns (Ferretti et al., 2018). Methodologically, we show that a subject-matched fusion design combined with SHAP-based (SHapley Additive exPlanations) site attribution can detect complementary information between body sites even when no measurable accuracy gain results. This is a pattern that conventional model comparison would misread as a null result. Gut (stool) composition alone achieved near-perfect classification (area under the receiver operating characteristic curve, AUC = 1.00), and combined stool-oral models never exceeded this ceiling. A null baseline, bootstrap confidence intervals, and preprocessing sensitivity checks confirmed that this ceiling reflects genuine biological signal rather than an artifact. Despite the flat accuracy curve, SHAP analysis of the fused model showed that oral cavity features carried more total feature importance than stool features (58.1% versus 41.9%), indicating that the model draws on real, non-redundant information from both sites. Biologically, the taxa driving this pattern include Malassezia restricta, Staphylococcus epidermidis, and Prevotella melaninogenica. These taxa behave in a manner consistent with their established roles as early colonizers of the neonatal gut, skin, and oral cavity, once their model-specific behavior is verified directly against abundance data rather than inferred from the literature alone. An independent, substantially larger paired-cohort study using a different analytical method reports a compatible pattern. Together, these results support a model of oral-gut microbiome maturation as two distinct, complementary processes, and demonstrate that detecting this kind of relationship requires examining a model's internal reasoning rather than its accuracy alone.

bioinformatics↗