Patricia Sullivan

Bioinformatics Scientist

Boston, Massachusetts, United States
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Summary

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Senior
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Patricia Sullivan is a bioinformatics scientist with eight years' experience specializing in splicing variant detection and tool development, currently based at Children’s National Hospital. She holds a PhD in Bioinformatics from UNSW and transitioned from doctoral research and a Fulbright placement at the Broad Institute into applied clinical genomics roles across pediatric cancer research. Her work blends computational method development with translational impact—prioritizing variants that alter RNA splicing and influence diagnosis or therapy decisions. Beyond research, she has led and mentored in scientific communities (serving as president of COMBINE Australia) and has a track record of teaching and outreach that bridges academia and clinical labs. Colleagues know her for turning complex transcriptomic signals into practical pipelines that accelerate variant interpretation.
code8 years of coding experience
bookBachelor of Science (Advanced) (Honours), Biotechnology and Genetics, Bachelor of Science (Advanced) (Honours), Biotechnology and Genetics at UNSW Australia
bookUNSW Sydney
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Stackoverflow

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Github Skills (9)

genomics9
bioinformatics9
pangolin7
genetics7
annotate2
database2
machine-learning2
visualization2
frontend1

Programming languages (7)

ShellRJavaScriptGoHTMLJupyter NotebookPython

Github contributions (5)

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CCICB/introme

Mar 2021 - Dec 2022

Introme prioritises coding and noncoding splice-altering variants for clinical variant interpretation
Contributions:1 release, 104 commits, 114 pushes in 1 year 10 months
bioinformaticsgenomicssplicing
pj-sullivan/Introme

Mar 2021 - Apr 2022

Contributions:6 pushes in 1 year 1 month
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