Aaron M. Wenger
Pacific Biosciences (United States)(US)
Publications by Year
Research Areas
Genomics and Phylogenetic Studies, Genomics and Rare Diseases, Genomic variations and chromosomal abnormalities, Cancer Genomics and Diagnostics, Genomics and Chromatin Dynamics
Most-Cited Works
- → GREAT improves functional interpretation of cis-regulatory regions(2010)4,934 cited
- → The complete sequence of a human genome(2022)3,193 cited
- → Accurate circular consensus long-read sequencing improves variant detection and assembly of a human genome(2019)1,887 cited
- → Variant Review with the Integrative Genomics Viewer(2017)1,230 cited
- → Multi-platform discovery of haplotype-resolved structural variation in human genomes(2019)1,025 cited
- → M-CAP eliminates a majority of variants of uncertain significance in clinical exomes at high sensitivity(2016)911 cited
- → Haplotype-resolved diverse human genomes and integrated analysis of structural variation(2021)776 cited
- → Human-specific loss of regulatory DNA and the evolution of human-specific traits(2011)555 cited
- → A robust benchmark for detection of germline large deletions and insertions(2020)472 cited
- → The complete sequence of a human Y chromosome(2023)431 cited