Complete Genomics (United States)

Recent papers from Complete Genomics (United States)

1. A little longer, a lot better: simulation-guided exploration of extended-length single-end barcoded reads for structural variant detectionBioinformatics Advances · 2026
2. Quantum mechanics-based multi-tensor AI/ML as predictor of patients' overall survival, gene targets, and drug responses from their glioblastoma tumors' whole genomes.Journal of Clinical Oncology · 2026
3. PharmVar GeneFocus: CYP1A2 —Clinical Impact, Genetic Variation, and Updated NomenclatureClinical Pharmacology & Therapeutics · 2026
4. Capture-C MPRA: A high-throughput method to simultaneously characterize promoter interactions and regulatory activity2025
5. A little longer, a lot better: simulation-guided exploration of extended-length single-end barcoded reads for structural variant detection2025
6. Large indel detection in region-based phased diploid assemblies from linked-readsBMC Genomics · 2025
7. Abstract 7560: Microsatellite instability (MSI) detection using flow-based sequencingCancer Research · 2024
8. Abstract 315: Cost-effective, comprehensive detection of gene fusions from DNA and RNA using the UG100 sequencerCancer Research · 2024
9. Abstract 4926: Advancements in somatic variant calling from UG100 whole genome and whole exome sequencing dataCancer Research · 2024
10. Abstract 2946: Characterizing the genomic landscapes of breast and lung tumors using cost-effective whole genome sequencingCancer Research · 2024
11. Assembly and analysis of the genome of Notholithocarpus densiflorusG3 Genes Genomes Genetics · 2024
12. A Germinal Center Checkpoint of AIRE in B Cells Limits Antibody Diversification2024
13. Assembly and analysis of the genome of Notholithocarpus densiflorus2023
14. A pan-MHC reference graph with 246 fully contiguous phased sequences2023
15. Acyl-CoA dehydrogenase substrate promiscuity limits the potential for development of substrate reduction therapy in disorders of valine and isoleucine metabolism2022
16. Retained introns in long RNA-seq reads are not reliably detected in sample-matched short readsGenome biology · 2022
17. Characterization and structure of the human lysine-2-oxoglutarate reductase domain, a novel therapeutic target for treatment of glutaric aciduria type 1Open Biology · 2022
18. Common genetic variation in KATNAL1 non‐coding regions is involved in the susceptibility to severe phenotypes of male infertilityAndrology · 2022
19. Characterization and structure of the human lysine-2-oxoglutarate reductase domain, a novel therapeutic target for treatment of glutaric aciduria type 12022
20. Rational evolution of a recombinant DNA polymerase for efficient incorporation of unnatural nucleotides by dual-site boosting2022