Francisco M De La Vega

10PUBLICATIONS
33CO-AUTHORS
Cancer geneticsGene expression (incl. microarray and other genome-wide approaches)Evolutionary computationSequence analysisGenomics and transcriptomics
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Publications (10)

|May 05, 2026
The Landscape of Genomic and Socioeconomic Variables in Patients with Colorectal Cancer Based on Genetic Ancestry.

|Apr 18, 2025
Benchmarking of germline copy number variant callers from whole genome sequencing data for clinical applications.

Francisco M De La Vega, Sean A Irvine, Pavana Anur

|Aug 13, 2024
Association of genetic ancestry with molecular tumor profiles in colorectal cancer.

Brooke Rhead, David M Hein, Yannick Pouliot

|Jul 07, 2023
A deep-learning-based RNA-seq germline variant caller.

Daniel E Cook, Aarti Venkat, Dennis Yelizarov

|Oct 14, 2021
Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases.

Francisco M De La Vega, Shimul Chowdhury, Barry Moore

|Apr 03, 2019
An open resource for accurately benchmarking small variant and reference calls.

Justin M Zook, Jennifer McDaniel, Nathan D Olson

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Frequent Collaborators

3 joint publications

Justin M Zook

2 joint publications

Paul C Boutros

2 joint publications

Christopher E Mason

2 joint publications

Benjamin L Moore