Andrew Carroll

Career Trajectory

Research Cluster Map

Direct collaborators. Node size = influence, colour = community, dashed = past collaboration.

• Two Australian genome assemblies expand the genomic blueprint of giant kelp

  BMC Genomics · 2026-06-12

• The Aboriginal community experience of the Virtual Rural Generalist Service in Western New South Wales: A yarning study

  First Nations Health and Wellbeing - The Lowitja Journal · 2026-03-19

• Aboriginal community researchers: A short report on the research training program and research experience with the Virtual Rural Generalist Service evaluation

  First Nations Health and Wellbeing - The Lowitja Journal · 2025-12-19

• Abstract 4358540: Machine Learning For Precision Phenotyping and Genomic Discovery for Heart Failure with Preserved Ejection Fraction

  Circulation · 2025-11-03

• Rapid, accurate long- and short-read mapping to large pangenome graphs with vg GiraffePreprint

  Research Square · 2025-10-23

• Accurate somatic small variant discovery for multiple sequencing technologies with DeepSomatic

  Nature Biotechnology · 2025-10-16 · 17 citations

• Rapid, accurate long- and short-read mapping to large pangenome graphs with vg GiraffePreprint

  bioRxiv (Cold Spring Harbor Laboratory) · 2025-10-01 · 3 citations

• A complete diploid human genome benchmark for personalized genomicsPreprint

  bioRxiv (Cold Spring Harbor Laboratory) · 2025-09-21 · 21 citations

• The Platinum Pedigree: a long-read benchmark for genetic variants

  Nature Methods · 2025-08-01 · 13 citations

• Accurate human genome analysis with element avidity sequencing

  BMC Bioinformatics · 2025-07-25 · 5 citations

• Applying multimodal AI to physiological waveforms improves genetic prediction of cardiovascular traits

  UNC Libraries · 2025-07-03

• Applying multimodal AI to physiological waveforms improves genetic prediction of cardiovascular traits

  The American Journal of Human Genetics · 2025-06-20 · 4 citations

• Pangenome-aware DeepVariantPreprint

  bioRxiv (Cold Spring Harbor Laboratory) · 2025-06-06 · 4 citations

• Highly accurate assembly polishing with DeepPolisher

  Genome Research · 2025-05-19 · 8 citations

• Abstract 2848: Severus: A tool for detecting and characterizing complex structural variants in cancer using long-read sequencing

  Cancer Research · 2025-04-21

• Abstract 7436: DeepSomatic: A SNV and small-indel somatic caller using deep neural networks

  Cancer Research · 2025-04-21

• Severus detects somatic structural variation and complex rearrangements in cancer genomes using long-read sequencing

  Nature Biotechnology · 2025-04-04 · 24 citations

• Small variant benchmark from a complete assembly of X and Y chromosomes

  Nature Communications · 2025-01-08 · 7 citations

• P775: KMT2A amplification in two adult patients with B-cell acute lymphoblastic leukemia

  Genetics in Medicine Open · 2025-01-01

• A robust benchmark for detecting low-frequency variants in the HG002 Genome In A Bottle NIST reference material.Preprint

  bioRxiv (Cold Spring Harbor Laboratory) · 2024-12-05 · 5 citations