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Abstract

The detection of recombination using consensus genome sequences has key limitations including failure to consider rare genetic variants and misidentification of artifactually assembled genome chimaeras as biological recombinants. However, commonly used recombination detection tools are not designed to directly analyse sequencing read data. Here, we present SRARec, a recombination detection tool that operates directly on raw reads. SRARec identifies polymorphic sites and applies the four-gamete test to detect recombination at the read level. The software incorporates mapping and quality filters and can analyse large repositories of raw sequencing data. Simulation validations showed that, given sufficient sequence diversity, SRARec can accurately detect recombination breakpoints. The consideration of rare variants makes SRARec particularly useful for detecting recombination in intra-host viral populations. Therefore, we applied the tool to 601,045 SARS-CoV-2 and 4,999 HIV-1 read datasets from the Sequence Read Archive (SRA, NCBI), enabling unprecedented genome-wide screening of intra-host recombination breakpoint signals at read-level resolution. Aggregating across all analysed datasets, the distribution of detected recombination breakpoint counts along genomes differed between these viruses, with pervasive breakpoint signals detectable in HIV-1 and sporadic clustered breakpoint hotspots in SARS-CoV-2. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=78 SRC="FIGDIR/small/741747v1_ufig1.gif" ALT="Figure 1"> View larger version (24K): org.highwire.dtl.DTLVardef@aa58fforg.highwire.dtl.DTLVardef@1b9061borg.highwire.dtl.DTLVardef@4010f1org.highwire.dtl.DTLVardef@1853e2_HPS_FORMAT_FIGEXP M_FIG C_FIG

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