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Cuypers, W. L.

Publications and source records attributed to Cuypers, W. L..

3 recordsLinked to original sources

SquiDBase: a community resource of raw nanopore data from microbes

Experimental data-driven research relies on raw data, which consist of unprocessed experimental outputs, whereas derived data are transformed through a number of processing steps to reveal specific insights. Such processing, however, can potentially introduce biases or information loss, compromising transparency and reproducibility. In nucleic acid sequencing, nucleotide sequences stored in the FASTQ format are widely shared, but FASTQ files are generated from platform-specific raw data outputs, which vary depending on the sequencing platform used. The raw data produced by Oxford Nanopore Technologies (ONT) sequencing devices contain valuable biological information and are also useful to improve data processing methods, which includes basecaller optimisation and modification detection. Increasing attention goes to exploring these raw signals to develop algorithms that could improve ONT device portability and enhance target enrichment efficiency through adaptive sampling. Despite these benefits, the storage and sharing of raw nanopore data remain limited due to technical constraints and the lack of appropriate, standardised and centralised infrastructure. To address this challenge, we developed SquiDBase (https://squidbase.org), a dedicated repository to collect raw microbial nanopore sequencing data. To maximise the utility of SquiDBase from its inception, we built SquiDPipe, a Nextflow pipeline for the automated removal of human or unwanted reads from raw nanopore data. Additionally, we sequenced 24 clinically relevant viruses and incorporated them into SquiDBase, significantly expanding the diversity of publicly available reference datasets. By offering a centralised, open-access raw data collection platform, SquiDBase facilitates data sharing, enhances reproducibility, and supports the development and benchmarking of novel computational tools, reinforcing open science in nanopore sequencing research.

bioinformatics↗

Selective whole-genome sequencing of Plasmodium parasites directly from blood samples by Nanopore adaptive sampling

BackgroundWhole-genome sequencing (WGS) is becoming an increasingly popular tool to study the population genetics and drug resistance of Plasmodium spp. However, the predominance of human DNA in a malaria patient blood sample requires time-consuming lab procedures to filter out human DNA or enrich Plasmodium DNA. Here, we investigated the potential of adaptive sampling to enrich for Plasmodium DNA while sequencing unenriched patient blood samples on a minION device. ResultsTo compare adaptive sampling versus regular sequencing, a dilution series consisting of 0% up to 100% P. falciparum DNA in human DNA was sequenced. Half of the flowcell channels were run in adaptive sampling mode, enriching for the P. falciparum reference genome, resulting in a 3.2 fold enrichment of P. falciparum bases on average. Samples with a lower concentration of parasite DNA had a higher enrichment potential. We confirmed these findings by sequencing two P. falciparum patient blood samples with common levels of parasitaemia (0.1% and 0.2%). The estimated enrichment was 3.9 and 5.8, which was sufficient to cover at least 97% of the P. falciparum reference genome at a median depth of 20 (highest parasitaemia) or 5 (lowest parasitaemia). A comparison of 38 drug resistance variants (WHO) obtained via adaptive sequencing or Sanger sequencing showed a high concordance between the two methods, suggesting that the obtained sequencing data is of sufficient quality to address common clinical research questions for patients with parasitaemias of 0.1% and higher. ConclusionsOur results demonstrate that adaptive Nanopore sequencing has the potential to replace more time-consuming Plasmodium-enrichment protocols and sequence directly from patient blood, given further improvements in cost-efficiency.

microbiology↗

No evidence for avoidance of black rat scent by the presumably less competitive Natal multimammate mouse in a choice experiment

In Africa, indigenous multimammate mice (Mastomys natalensis) only appear to live commensally in houses when invasive black rats (Rattus rattus) are absent, yet little is known about the underlying mechanism. Avoidance through smell may cause the absence of M. natalensis from areas occupied by R. rattus, but this hypothesis has not yet been tested. We conducted a Y-maze choice experiment where 15 M. natalensis were offered a choice between corridors containing conspecific scent, R. rattus scent, and a control scent. Residence time in the R. rattus corridor was greater than that in the control corridor but equal to that in the M. natalensis corridor, suggesting that multimammate mice do not actively avoid the scent of their invasive competitor.

zoology↗