Robert Syme is a Scientific Support Lead and bioinformatics specialist with 15 years of experience bridging molecular biology, genomics and data engineering. Based in Montreal, he has progressed from academic research and postdoctoral work into industry roles at McGill and Deel, where he moved from Bioinformatics Engineer to leading scientific support. He is a hands-on contributor to high-profile open-source pipelines like nf-core/scrnaseq, improving data accuracy and workflow robustness through back-end, DevOps and Nextflow work. Passionate about open data and decentralised publishing, he combines practical tooling (samplesheet checks, GTF filtering, Salmon/index fixes) with clear technical writing and documentation improvements. Known for integrating wet-lab insight with scalable computational pipelines, he brings a rare mix of domain expertise, reproducible workflows and operational support.
15 years of coding experience
7 years of employment as a software developer
BSc, Molecular Biology, H1 (First class), BSc, Molecular Biology, H1 (First class) at Murdoch University
Doctor of Philosophy (Ph.D.), Bioinformatics, Doctor of Philosophy (Ph.D.), Bioinformatics at Curtin University
Contributions:19 reviews, 11 commits, 26 PRs in 8 years 2 months
Contributions summary:Robert primarily contributed to the project by correcting typos and making minor wording adjustments within the documentation files. These changes were focused on improving the clarity and accuracy of the documentation, specifically within the `docs` directory. The edits include fixing grammatical errors, updating links, and improving the examples presented in the documentation, ensuring better understanding for users. The work also included adjustments to code examples to align them with the latest versions.
Single-cell RNA-Seq pipeline for barcode-based protocols such as 10x, DropSeq or SmartSeq, offering a variety of aligners and empty-droplet detection
Role in this project:
Back-end Developer & DevOps Engineer
Contributions:2 releases, 5 reviews, 15 commits in 24 days
Contributions summary:Robert significantly contributed to the nf-core/scrnaseq pipeline, focusing on enhancing its functionality and robustness. They added a Python function for samplesheet checks and implemented a filter to remove extraneous features from GTF files, improving data processing accuracy. Additionally, the user addressed a bug related to the Salmon index and made changes to integrate with iGenome for data retrieval. These changes also involved updating module definitions and workflow configurations within the Nextflow pipeline, as well as whitespace and linting fixes.
nf-core10xrnaseqpipelinegenomics-data
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