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Bruand, J.

Publications and source records attributed to Bruand, J..

3 recordsLinked to original sources

Isocall enables scalable transcript identification from long-read RNA-sequencing data

Long-read RNA sequencing directly resolves the full structures of RNA transcripts. Advances in throughput now enable the generation of deeply sequenced cohorts of hundreds of samples, making joint transcript discovery across large datasets possible. However, existing transcript identification methods were designed for small datasets, which limits their applicability at this scale. Here, we present Isocall, a scalable and deterministic computational method for jointly calling transcripts from multiple PacBio long-read RNA sequencing samples. Isocall converts aligned full-length non-concatemer reads into compact per-sample transcript profiles, merges these profiles across samples, and jointly identifies known and novel transcripts supported by reads in the analyzed dataset. Filtering is tunable: presets provide coarse control and individual parameters, including relative abundance and internal priming thresholds, provide fine control. Isocall demonstrated high precision in our accuracy benchmarks, including the WTC11 SIRV spike-in controls, for which Isocall reported 0-2 false-positive transcripts per sample across the three SIRV mixes at default settings. To demonstrate scalability, we applied Isocall to 206 samples, totalling 3.5 billion raw reads, from the Human Pangenome Reference Consortium. After parallelized pbmm2 alignment and Isocall profile, the call step performed joint calling across the entire dataset in 25 minutes, using 1.3 GB of peak memory and 8 threads. Finally, in Genome in a Bottle samples with matched SNP genotypes, splice-site polymorphisms provide an additional measure of call accuracy: Isocall recovered 337 polymorphic splice sites, including a de novo donor site in BTN3A1 that corresponds to a complete isoform switch on the mutant allele.

bioinformatics↗

LRP2: A proteogenomics pipeline for long-read informed protein isoform analysis and discovery

Most human genes produce multiple RNA isoforms, yet it remains unclear which isoforms are translated into stable, functional proteins. Long-read RNA sequencing resolves full-length transcript structures and, when paired with mass spectrometry, can provide empirical evidence of isoform translation. Despite this opportunity, comprehensive workflows integrating isoform discovery, open reading frame prediction, peptide identification, and protein inference remain limited, leaving users to handle these steps piecemeal. Here, we present LRP2, a modular, end-to-end long-read proteogenomics pipeline built in Nextflow. LRP2 scales transcript discovery to hundreds of samples via PacBio's latest Isocall tool, removes technical artifacts with SQANTI QC, generates and classifies predicted proteomes via CPAT and SQANTI Protein, performs multi-group differential expression and usage analysis via edgeR, DRIMSeq, and a long-read adaptation of LeafCutter, and integrates protein-level evidence from DDA and DIA MS data through FragPipe. For cross-dataset comparison of novel isoforms, LRP2 employs deterministic splice-junction, coordinate-based isoform identifiers. Used as an integrated pipeline, LRP2 enables the detection of novel peptides and improves the protein isoform inference to confirm protein isoform translation.

bioinformatics↗

A framework for evaluating edited cell libraries created by massively parallel genome engineering

Genome engineering methodologies are transforming biological research and discovery. Approaches based on CRISPR technology have been broadly adopted and there is growing interest in the generation of massively parallel edited cell libraries. Comparing the libraries generated by these varying approaches is challenging and researchers lack a common framework for defining and assessing the characteristics of these libraries. Here we describe a framework for evaluating massively parallel libraries of edited genomes based on established methods for sampling complex populations. We define specific attributes and metrics that are informative for describing a complex cell library and provide examples for estimating these values. We also connect this analysis to generic phenotyping approaches, using either pooled (typically via a selection assay) or isolate (often referred to as screening) phenotyping approaches. We approach this from the context of creating massively parallel, precisely edited libraries with one edit per cell, though the approach holds for other types of modifications, including libraries containing multiple edits per cell (combinatorial editing). This framework is a critical component for evaluating and comparing new technologies as well as understanding how a massively parallel edited cell library will perform in a given phenotyping approach.

genomics↗