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Peer-reviewed and preprint publications demonstrating the real-world applications of our technology.

Nature BiotechnologyApril 2025David Porubsky, et al. Human de novo mutation rates from a four-generation pedigree reference
Using advanced sequencing technologies, the authors assembled near-complete genomes across four generations of the CEPH 1463 pedigree to investigate human de novo mutation (DNM) rates. AVITI sequencing provided high-accuracy data in homopolymer regions that improved validation of tandem repeat mutations and helped reduce artifacts in variant calling.
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BioRxivNovember 2024Kevin Green, et al. Flexible, Production-scale, Human Whole Genome Sequencing on a Benchtop Sequencer
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BioRxivNovember 2024Paul-Lennard Mendez, et al. Atheroprone Flow Activates SMAD-FOXO1 to drive Endothelial-to-Mesenchymal Transition and Atherosclerosis
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BioRxivNovember 2024Barbara Bayer, et al. Contribution of ammonia oxidizers to inorganic carbon fixation in the dark ocean
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Redox BiologyNovember 2024Janice Raabe, et al. Physioxia rewires mitochondrial complex composition to protect stem cell viability
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BioRxivNovember 2024Yiyang Zhou, et al. SARS-CoV-2 EndoU-ribonuclease regulates RNA recombination and impacts viral fitness
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BioRxivNovember 2024Thomas J Degroat, et al. Chronic variable mild stress alters the transcriptome and signaling properties of the anterodorsal bed nuceleus of the stria terminalis in a sex-dependent manner
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Research SquareNovember 2024Mazhar Adli, et al. Comparative analysis and directed protein evolution yield an improved degron technology with minimal basal degradation, rapid inducible depletion, and faster recovery of target proteins
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Nature CommunicationsNovember 2024Melanie Massonnet, et al. Evolutionary history of the grape sex-determining region in angiosperms and emergence of dioecy in Vitaceae
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BioRxivNovember 2024Katharine Cecchini, et al. Mouse Pachytene piRNAs Cleave Hundreds of Transcripts, But Alter the Steady-State Abundance of Only a Minority of Targets
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Molecular Biology and EvolutionNovember 2024Beryl M Jones, et al. Repeated shifts in sociality are associated with fine-tuning of highly conserved and lineage-specific enhancers in a socially flexible bee
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CellNovember 2024Bo Zhou, et al. Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders
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PNASNovember 2024Simon Roubille, et al. The HUSH epigenetic repressor complex silences PML nuclear bodies-associated HSV-1 quiescent genomes
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BMC GenomicsNovember 2024Anna L. Mcdonald, et al. Efficient small fragment sequencing of human, cow, and bison miRNA, small RNA or csRNA-seq libraries using AVITI
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Acta NeurologicaNovember 2024Nainika Roy, et al. Elevated expression of the retrotransposon LINE-1 drives Alzheimer’s disease-associated microglial dysfunction
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Nature GeneticsNovember 2024Andrew A Perez, et al. ChIP-DIP maps binding of hundreds of proteins to DNA simultaneously and identifies diverse gene regulatory elements
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International Journal of Molecular SciencesNovember 2024Eloho Ighofose, et al. Effect of Long-Term Cisplatin Exposure on the Proliferative Potential of Immortalized Renal Progenitor Cells
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Nature CommunicationsNovember 2024Liselot Dewachter, et al. The role of the essential GTPase ObgE in regulating lipopolysaccharide synthesis in Escherichia coli
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BioRxivOctober 2024Yuya Kiguchi, et al. Giant extrachromosomal element “Inocle” potentially expands the adaptive capacity of the human oral microbiome
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BioRxivOctober 2024Verena Haage, et al. HDAC Inhibitors recapitulate Human Disease-Associated Microglia Signatures in vitro
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Scientific dataOctober 2024Jennifer H. McDaniel, et al. Development and extensive sequencing of a broadly-consented Genome in a Bottle matched tumor-normal pair
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PLOS OneOctober 2024Pooja Biswas, et al. Avidity sequencing of whole genomes from retinal degeneration pedigrees identifies causal variants
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ACS NanoOctober 2024Kewa Gao, et al. Widespread Gene Editing in the Brain via In Utero Delivery of mRNA Using Acid-Degradable Lipid Nanoparticles
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Acta NeurologicaOctober 2024Celeste Laureyssen, et al. Hypothesis-based investigation of known AD risk variants reveals the genetic underpinnings of neuropathological lesions observed in Alzheimer’s-type dementia
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Cell ReportsOctober 2024Pavel Tsaytler, et al. SRF promotes long-range chromatin loop formation and stem cell pluripotency
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Journal of Biological ChemistryOctober 2024Julia A. Jones, et al. Murine Nuclear Tyrosyl-tRNA Synthetase Deficiency Leads to Fat Storage Deficiency and Hearing Loss
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226 - 250 of 290 publications