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Spies, N.

Publications and source records attributed to Spies, N..

6 recordsLinked to original sources

Caris-ComBat-seq: Directionally Harmonizing Large-Scale RNA-seq Datasets

BackgroundBulk RNA sequencing (RNA-seq) is an essential research and clinical diagnostics tool capable of uncovering biological insights across experimental conditions, sample types and diseases at scale. However, RNA-seq data is sensitive to batch effects introduced by technical variation. Harmonizing expression (or batch-correcting) is critical when analyzing measurements from different RNA-seq platforms. In the context of oncology, efficiently and accurately harmonizing expression at scale is important for harnessing massively large datasets (hundreds of thousands of samples) of tumor molecular profiles from different assay platforms. We aimed to develop a method for harmonizing expression in this challenging context. ResultsHere, we extend the widely used ComBat-seq method, as implemented in the pyComBat tool, to enable three key advances: (i) directionally adjusting counts from one batch towards a reference batch, rather than an average expression profile, (ii) separating the training and adjusting steps so that newly profiled samples not available at the time of initial model training can be harmonized, and (iii) flexibly handling outliers to improve the quality of harmonized counts. The resulting model correctly learns gene-specific differences between assay platforms and can near-instantaneously harmonize individual samples. We validated the use of the Caris-ComBat-seq tool to harmonize RNA-seq measurements on a benchmarking dataset of [~]10,000 TCGA tumor samples. Finally, we demonstrated its strength for very large datasets, by harmonizing RNA-seq data from nearly half a million tumor samples profiled by two different next-generation sequencing assays in Caris Life Sciences clinical laboratory. Source code, tutorials and manuscript data are available at: https://github.com/Caris-Life-Sciences/Caris-ComBat-seq and https://doi.org/10.5281/zenodo.17154014. ConclusionsWe present Caris-ComBat-seq, a new variant of the ComBat-seq algorithm designed to harmonize count-based expression data in the context of high-throughput profiling laboratories. It offers the same ability to ameliorate batch effects and retain biological signal as the original ComBat-seq, with additional operational flexibility and scaling that benefits its high-throughput application.

bioinformatics↗

A longitudinal single-cell therapeutic atlas of anti-tumour necrosis factor treatment in inflammatory bowel disease

Precision medicine in immune-mediated inflammatory diseases (IMIDs) requires an understanding of how cellular networks change following therapy. We describe a therapeutic atlas for Crohns disease (CD) and ulcerative colitis (UC) following anti-tumour necrosis factor (TNF) therapy. We generated ~1 million single-cell transcriptomes, organised into 109 cell states, from 216 gut biopsies from 38 patients and three controls, revealing disease- and therapy-specific differences. A systems-biology analysis identified distinct spatially-resolved cellular microenvironments: granuloma signatures in CD and interferon (IFN)-response signatures localising to T-cell aggregates and epithelial damage in CD and UC. Longitudinal comparisons demonstrated that disease progression in non-responders associated with myeloid and stromal cell perturbations in CD and increased multi-cellular IFN signalling in UC. IFN signalling was also observed in rheumatoid arthritis (RA) synovium with a lymphoid pathotype. Our therapeutic atlas informs drug positioning across IMIDs, and suggests a rationale for the use of janus kinase (JAK) inhibition following anti-TNF resistance.

immunology↗

SVCurator: A Crowdsourcing app to visualize evidence of structural variants for the human genome

A high quality benchmark for small variants encompassing 88 to 90% of the reference genome has been developed for seven Genome in a Bottle (GIAB) reference samples. However a reliable benchmark for large indels and structural variants (SVs) is yet to be defined. In this study, we manually curated 1235 SVs which can ultimately be used to evaluate SV callers or train machine learning models. We developed a crowdsourcing app - SVCurator - to help curators manually review large indels and SVs within the human genome, and report their genotype and size accuracy.\n\nSVCurator is a Python Flask-based web platform that displays images from short, long, and linked read sequencing data from the GIAB Ashkenazi Jewish Trio son [NIST RM 8391/HG002], We asked curators to assign labels describing SV type (deletion or insertion), size accuracy, and genotype for 1235 putative insertions and deletions sampled from different size bins between 20 and 892,149 bp. The crowdsourced results were highly concordant with 37 out of the 61 curators having at least 78% concordance with a set of expert curators, where there was 93% concordance amongst expert curators. This produced high confidence labels for 935 events. When compared to the heuristic-based draft benchmark SV callset from GIAB, the SVCurator crowdsourced labels were 94.5% concordant with the benchmark set. We found that curators can successfully evaluate putative SVs when given evidence from multiple sequencing technologies.

genomics↗

Haplotype-resolved and integrated genome analysis of ENCODE cell line HepG2

The HepG2 cancer cell line is one of the most widely-used biomedical research and one of the main cell lines of ENCODE. Vast numbers of functional genomics and epigenomics datasets have been produced to characterize its biology. However, the correct interpretation such data requires an understanding of the cell lines genome sequence and genome structure. Using a variety of sequencing and analysis methods, we identified a wide spectrum of HepG2 genome characteristics: copy numbers of chromosomal segments, SNVs and Indels (corrected for aneuploidy), phased haplotypes extending to entire chromosome arms, loss of heterozygosity, retrotransposon insertions, structural variants (SVs) including complex and somatic genomic rearrangements. We also identified allele-specific expression and DNA methylation genome-wide and assembled an allele-specific CRISPR/Cas9 targeting map.\n\nSIGNIFICANCEHaplotype-resolved and comprehensive whole-genome analysis of a widely-used cell line for cancer research and ENCODE, HepG2, serves as an essential resource for unlocking complex cancer gene regulation using a genome-integrated framework and also provides genomic context for the analysis of ~1,000 functional datasets to date on ENCODE for biological discovery. We also demonstrate how deeper insights into genomic regulatory complexity are gained by adopting a genome-integrated framework.

genomics↗

genomeview - an extensible python-based genomics visualization engine

Visual inspection and analysis is integral to quality control, hypothesis generation, methods development and validation of genomic data. The richness and complexity of genomic data necessitates customized visualizations highlighting specific features of interest while hiding the often vast tide of irrelevant attributes. However, the majority of genome-visualization occurs either in general-purpose tools such as IGV (Robinson et al, 2011) or the UCSC Genome Browser (Kent et al, 2002) - which offer many options to adjust visualization parameters, but very little in the way of extensibility - or narrowly-focused tools aiming to solve a single visualization problem. Here, we present genomeview, a python-based visualization engine which is easy to extend and simple to integrate into existing analysis pipelines.

genomics↗

Comprehensive, Integrated, and Phased Whole-Genome Analysis of the Primary ENCODE Cell Line K562

K562 is widely used in biomedical research. It is one of three tier-one cell lines of ENCODE and also most commonly used for large-scale CRISPR/Cas9 screens. Although its functional genomic and epigenomic characteristics have been extensively studied, its genome sequence and genomic structural features have never been comprehensively analyzed. Such information is essential for the correct interpretation and understanding of the vast troves of existing functional genomics and epigenomics data for K562. We performed and integrated deep-coverage whole-genome (short-insert), mate-pair, and linked-read sequencing as well as karyotyping and array CGH analysis to identify a wide spectrum of genome characteristics in K562: copy numbers (CN) of aneuploid chromosome segments at high-resolution, SNVs and Indels (both corrected for CN in aneuploid regions), loss of heterozygosity, mega-base-scale phased haplotypes often spanning entire chromosome arms, structural variants (SVs) including small and large-scale complex SVs and non-reference retrotransposon insertions. Many SVs were phased, assembled, and experimentally validated. We identified multiple allele-specific deletions and duplications within the tumor suppressor gene FHIT. Taking aneuploidy into account, we re-analyzed K562 RNA-seq and whole-genome bisulfite sequencing data for allele-specific expression and allele-specific DNA methylation. We also show examples of how deeper insights into regulatory complexity are gained by integrating genomic variant information and structural context with functional genomics and epigenomics data. Furthermore, using K562 haplotype information, we produced an allele-specific CRISPR targeting map. This comprehensive whole-genome analysis serves as a resource for future studies that utilize K562 as well as a framework for the analysis of other cancer genomes.

genomics↗