Giuseppe Narzisi

Career Trajectory

Research Cluster Map

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

• A complete human pancreatic cancer genome

  bioRxiv (Cold Spring Harbor Laboratory) · 2026-05-06 · 1 citations

• The New York Genome Center ALS Consortium resource integrates postmortem tissue transcriptomics and whole genome sequencing to empower biological discovery

  medRxiv · 2026-05-04 · 1 citations

• Abstract 1510: CASTLE: long-read sequencing panel of cancer cell lines to improve standards of somatic variant calling and benchmarking

  Cancer Research · 2026-04-03

• Lancet2: Improved and accelerated somatic variant calling with joint multi-sample local assembly graphs

  NAR Genomics and Bioinformatics · 2026-03-25

• Structural Variants Associated with Sporadic Alzheimer's Disease Pathologies and Segregates in Caribbean Hispanics and Non‐Hispanic White Families

  Alzheimer s & Dementia · 2025-12-01

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

  Nature Biotechnology · 2025-10-16 · 17 citations

• Comprehensive benchmarking of somatic single-nucleotide variant and indel detection at ultra-low allele fractions using short- and long-read dataPreprint

  bioRxiv (Cold Spring Harbor Laboratory) · 2025-10-14 · 1 citations

• Correction: Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair

  Scientific Data · 2025-08-08

• Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair

  Scientific Data · 2025-07-16 · 9 citations

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

  Cancer Research · 2025-04-21

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

  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

• Lancet2: Improved and accelerated somatic variant calling with joint multi-sample local assembly graphsPreprint

  bioRxiv (Cold Spring Harbor Laboratory) · 2025-02-23 · 1 citations

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

  Nature Communications · 2025-01-08 · 7 citations

• Beyond GWAS: Investigating Structural Variants and Their Segregation in Familial Alzheimer’s Disease

  Alzheimer s & Dementia · 2024-12-01

• Efficient indexing and querying of annotations in a pangenome graphPreprint

  bioRxiv (Cold Spring Harbor Laboratory) · 2024-10-15 · 4 citations

• Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pairPreprint

  bioRxiv (Cold Spring Harbor Laboratory) · 2024-09-22 · 6 citations

• DeepSomatic: Accurate somatic small variant discovery for multiple sequencing technologiesPreprint

  bioRxiv (Cold Spring Harbor Laboratory) · 2024-08-19 · 17 citations