Francisco M. De La Vega
Stanford University(US)
Publications by Year
Research Areas
Cancer Genomics and Diagnostics, Genomics and Rare Diseases, Genomics and Phylogenetic Studies, Genetic Associations and Epidemiology, Genetic factors in colorectal cancer
Most-Cited Works
- → Genomics for the world(2011)624 cited
- → Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding(2009)519 cited
- → Best practices for benchmarking germline small-variant calls in human genomes(2019)489 cited
- → An open resource for accurately benchmarking small variant and reference calls(2019)447 cited
- → Spectrum and prevalence of genetic predisposition in medulloblastoma: a retrospective genetic study and prospective validation in a clinical trial cohort(2018)389 cited
- → Comparing Variant Call Files for Performance Benchmarking of Next-Generation Sequencing Variant Calling Pipelines(2015)263 cited
- → Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases(2021)141 cited
- → Polygenic risk scores: a biased prediction?(2018)138 cited
- → Population Genetic Inference from Personal Genome Data: Impact of Ancestry and Admixture on Human Genomic Variation(2012)110 cited
- → Joint Variant and De Novo Mutation Identification on Pedigrees from High-Throughput Sequencing Data(2014)90 cited