Maria Nattestad
Google (United States)(US)
Publications by Year
Research Areas
Genomics and Phylogenetic Studies, Genomics and Rare Diseases, Cancer Genomics and Diagnostics, Chromosomal and Genetic Variations, Genomic variations and chromosomal abnormalities
Most-Cited Works
- → Phased diploid genome assembly with single-molecule real-time sequencing(2016)2,186 cited
- → GenomeScope: fast reference-free genome profiling from short reads(2017)1,908 cited
- → Accurate detection of complex structural variations using single-molecule sequencing(2018)1,893 cited
- → A draft human pangenome reference(2023)1,069 cited
- → Assemblytics: a web analytics tool for the detection of variants from an assembly(2016)432 cited
- → Haplotype-aware variant calling with PEPPER-Margin-DeepVariant enables high accuracy in nanopore long-reads(2021)311 cited
- → Pangenome graph construction from genome alignments with Minigraph-Cactus(2023)276 cited
- → Complex rearrangements and oncogene amplifications revealed by long-read DNA and RNA sequencing of a breast cancer cell line(2018)226 cited
- → Ultrarapid Nanopore Genome Sequencing in a Critical Care Setting(2022)212 cited
- → PrecisionFDA Truth Challenge V2: Calling variants from short and long reads in difficult-to-map regions(2022)198 cited