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Staut, J.

Publications and source records attributed to Staut, J..

2 recordsLinked to original sources

MINI-EX version 2: cell-type-specific gene regulatory network inference using an integrative single-cell transcriptomics approach

Understanding and predicting cell-type-specific gene regulatory networks (GRNs) is essential for unraveling the complex interactions between transcription factors (TFs) that modulate the expression of target genes and control diverse biological processes in multicellular organisms. MINI-EX (Motif-Informed Network Inference based on single-cell EXpression data) is an integrative tool tailored for identifying cell-type-specific GRNs in plants. Leveraging single-cell transcriptomics data, MINI-EX constructs expression-based networks and integrates TF motif information to produce GRNs with increased accuracy. Furthermore, it assigns regulatory modules to distinct cell types and prioritizes candidate regulators by employing a strategy that encompasses network centrality measures, functional annotations, and expression specificity. Taken together, MINI-EX offers a powerful approach to identify cell-type-specific transcriptional cascades and enhance our understanding of TF functions in plant biology. Here, we discuss recent advancements in the tools latest version and explain how single-cell GRNs can be identified for non-model species lacking TF motif information. Additionally, we provide a comprehensive guide to use MINI-EX, covering the entire pipeline from preparing input files starting from a single-cell experiment, over configuring parameters, to interpreting output data.

plant biology↗

Benchmark of tools for in silico prediction of MHC class I and class II genotypes from NGS data

The Human Leukocyte Antigen (HLA) genes are a group of highly polymorphic genes that are located in the Major Histocompatibility Complex (MHC) region on chromosome 6. The HLA genotype affects the presentability of tumour antigens to the immune system. While knowledge of these genotypes is of utmost importance to study differences in immune responses between cancer patients, gold standard, PCR-derived genotypes are rarely available in large Next Generation Sequencing (NGS) datasets. Therefore, a variety of methods for in silico NGS-based HLA genotyping have been developed, bypassing the need to determine these genotypes with separate experiments. However, there is currently no consensus on the best performing tool. Here, we compiled a list of 13 HLA callers and evaluated their accuracy on three different datasets. Based on these results, best-practice guidelines were constructed, and consensus HLA allele predictions were made for DNA and RNA samples from The Cancer Genome Atlas (TCGA).

bioinformatics↗