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Last updated on 2025-06-23.

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David Zhang

Bioinformatics software engineer with experience operating across the entire software development lifecycle. Skilled in prototyping and benchmarking innovative solutions, as well as implementing, testing, and integrating software into production-ready pipelines.

Work Experience

Senior bioinformatics engineer

CoSyne Therapeutics

London, UK (hybrid)

Present - 2024

  • Optimised and scaled machine learning tools to extract actionable insights from single-cell Perturb-seq datasets comprising millions of cells. Directed the project end-to-end, integrating findings to inform strategic decisions and guide company direction.
  • Designed and deployed a robust data pipeline that ingested, tidied and version-controlled data for the Neo4j knowledge graph. Automated the deployment of this graph via CI/CD using Terraform, enabling automated releases to AWS enhancing reproducibility and operational efficiency.

Senior bioinformatics software engineer

Congenica

Hinxton, UK (hybrid)

2024 - 2022

  • Designed, benchmarked, and productionized scalable bioinformatics pipelines in Nextflow to process solid tumor sequencing data. Pipelines included alignment, variant calling, driver mutation annotation, and therapy matching, supporting clinical and translational applications.
  • Built a suite of Python and R packages to automate the clinical verification process, enabling earlier detection and resolution of issues. This automation reduced verification time by from 1 month per quarterly release, significantly accelerating the development cycle.

Bioinformatician internship (2 months)

Verge Genomics

London, UK (remote)

2021

  • Created a reproducible aberrant splicing detection pipeline using docker for drug target discovery in C9orf72 ALS patients.

Education

PhD, Bioinformatics

University College London

London, UK

2022 - 2017

  • Thesis: Using transcriptomics to improve the genetic diagnosis rate of rare disease patients.
  • Developed ggtranscript, an open-source R package for visualizing transcript structures, which has recieved 150+ stars on GitHub and 250+ citations.

MSc, Neuroscience

University College London

London, UK

2016 - 2015

  • Thesis: The role of mitochondrial dysfunction in Xerodoma pigmentosum
  • Grade: Merit (68%)
  • Awarded post-graduate support scheme bursary (£10,000)

BSc, Biomedical science

University College London

London, UK

2015 - 2012

  • Thesis: Investigating the function of CYFIP1 in the development of rat hippocampal neurons.
  • Grade: 2:1 (69%)

H.S.

Queen Elizabeth’s School

Barnet, UK

2012 - 2007

  • Grades: Maths (A*), Biology (A*), Chemistry (A*), Sociology (A).

Software & programming

Portfolio website

N/A

N/A

Present - 2022

  • My website is built using Django/Bootstrap 5, deployed with Heroku and showcases the five projects I’m most fond of.

Rust packages

N/A

N/A

2024

  • tuni: Unify transcripts across different samples. Author.

Python packages

N/A

N/A

2023 - 2021

  • codino converts a codon design to the expected amino acid frequencies, and vice versa. Author.
  • autogroceries: Use Selenium to automate your grocery shop. Author.
  • stravaboard: A dashboard for flexibly displaying and tracking Strava runs built using Streamlit. Author.

R packages

N/A

N/A

2022 - 2020

  • ggtranscript: Visualising transcript structure and annotation using ggplot2. Author.
  • megadepth: BigWig and BAM related utilities. An R wrapper for the megadepth software developed by Chris Wilks. Co-author.
  • dasper: Detection of aberrant splicing events in RNA-sequencing. Author,

Selected Publications

A complete list of publications is available via Google Scholar

ggtranscript: an R package for the visualization and interpretation of transcript isoforms using ggplot2

Bioinformatics

N/A

2022

Developmental Consequences of Defective ATG7-Mediated Autophagy in Humans

The New England Journal of Medicine

N/A

2021

  • Collier J, Guissart C, Oláhová M, Sasorith S, Piron-Prunier F, Suom Fi, Zhang D, Martinez-Lopez N, Leboucq N, Bahr A, Azzarello-Burri S, Reich S, Schöls L, Polvikoski TM, Meyer P, Larrieu L, Schaefer AM, Alsaif HS, Alyamani S, Zuchner S, Barbosa IA, Deshpande C, Pyle A, Rauch A, Synofzik M, Alkuraya FS, Rivier F, Ryten M, McFarland R, Delahodde A, McWilliams TG, Koenig M, and Taylor RW.
  • Role: Co-first author
  • DOI: https://doi.org/10.1093/bioinformatics/btac409

Megadepth: efficient coverage quantification for BigWigs and BAMs

Bioinformatics

N/A

2021

Incomplete annotation of disease-associated genes is limiting our understanding of Mendelian and complex neurogenetic disorders.

Science advances

N/A

2020

  • Zhang D, Guelfi S, Ruiz SG, Costa B, Reynolds RH, D’Sa K, Liu W, Courtin T, Peterson A, Jaffe AE, Hardy J, Botia JA, Collado-Torres L and Ryten M.
  • Role: First Author.
  • DOI: https://doi.org/10.1126/sciadv.aay8299