Sign in
BioinformaticsPLoS Computational Biology
Peer-reviewed journal article

nf-core/airrflow: an adaptive immune receptor repertoire analysis workflow employing the Immcantation framework

Gisela GabernetiD, Susanna MarqueziD, Robert D. Bjornson, Alexander PeltzeriD, Hailong MengiD, Edel AroniD, Noah Yann LeeiD, Cole G. JenseniD, David Ladd, Mark PolsteriD, Friederike HansseniD, Simon HeumosiD, nf-core community, Gur YaariiD, Markus Christian KowarikiD, Sven NahnseniD, Steven H. KleinsteiniD

Abstract

Adaptive Immune Receptor Repertoire sequencing (AIRR-seq) is a valuable experimental tool to study the immune state in health and following immune challenges such as infectious diseases, (auto)immune diseases, and cancer. Several tools have been developed to reconstruct B cell and T cell receptor sequences from AIRR-seq data and infer B and T cell clonal relationships. However, currently available tools offer limited parallelization across samples, scalability or portability to high-performance computing infrastructures. To address this need, we developed nf-core/airrflow, an end-to-end bulk and single-cell AIRR-seq processing workflow which integrates the Immcantation Framework following BCR and TCR sequencing data analysis best practices. The Immcantation Framework is a comprehensive toolset, which allows the processing of bulk and single-cell AIRR-seq data from raw read processing to clonal inference. nf-core/airrflow is written in Nextflow and is part of the nf-core project, which collects community contributed and curated Nextflow workflows for a wide variety of analysis tasks. We assessed the performance of nf-core/airrflow on simulated sequencing data with sequencing errors and show example results with real datasets. To demonstrate the applicability of nf-core/airrflow to the high-throughput processing of large AIRR-seq datasets, we validated and extended previously reported findings of convergent antibody responses to SARS-CoV-2 by analyzing 97 COVID-19 infected individuals and 99 healthy controls, including a mixture of bulk and single-cell sequencing datasets. Using this dataset, we extended the convergence findings to 20 additional subjects, highlighting the applicability of nf-core/airrflow to validate findings in small in-house cohorts with reanalysis of large publicly available AIRR datasets. Availability and implementationnf-core/airrflow is available free of charge, under the MIT license on GitHub (https://github.com/nf-core/airrflow). Detailed documentation and example results are available on the nf-core website at (https://nf-co.re/airrflow). Visual abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=100 SRC="FIGDIR/small/576147v2_ufig1.gif" ALT="Figure 1"> View larger version (24K): org.highwire.dtl.DTLVardef@e39504org.highwire.dtl.DTLVardef@14c52aforg.highwire.dtl.DTLVardef@1c87664org.highwire.dtl.DTLVardef@1d4d78b_HPS_FORMAT_FIGEXP M_FIG C_FIG

PDFDOICode

02 /Specification & Classification

Click any tag to browse matching papers
Citations
23
FWCI
3.85
Field percentile
top 5%

Reproducibility ledger

Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.

Sign in to file a reproducibility report.

Similarity Map
SelectedSame fieldCross-field
THISWaltari '22Abdollahi '26Rognes '22Mhanna '25Bagordo '26Sutherland '23
62% semantic matchImmunology
E. Waltari, S. Nafees, J. Wong+2 more·PLOS Computational Biology·Sep 20, 2022