2022 - Research.com Best Female Scientist Award
2022 - Research.com Best Scientist Award
Her primary areas of investigation include Genetics, Exome, Cancer research, Gene and Single-nucleotide polymorphism. Her work in Haplotype, Genome, Human genome, Genome-wide association study and Genomics are all subfields of Genetics research. Her Exome research incorporates elements of Molecular genetics, Cancer and Mutation rate.
The study incorporates disciplines such as DNA methylation, Transcriptome, IDH1, CDKN2A and Gefitinib in addition to Cancer research. As a part of the same scientific family, Stacey Gabriel mostly works in the field of Gene, focusing on Adenocarcinoma and, on occasion, Lung cancer. Her work carried out in the field of Single-nucleotide polymorphism brings together such families of science as Evacetrapib and Cholesterol.
Stacey Gabriel spends much of her time researching Genetics, Cancer research, Gene, Exome sequencing and Exome. Her Genetics research focuses on Genome-wide association study, Single-nucleotide polymorphism, Mutation, Genome and Genetic association. Her Genome research focuses on Computational biology and how it connects with Genomics and Genetic variation.
The Cancer research study combines topics in areas such as DNA methylation, Somatic cell, Carcinogenesis, Colorectal cancer and PTEN. Her research integrates issues of Internal medicine and Point mutation in her study of Exome sequencing. Stacey Gabriel works mostly in the field of Exome, limiting it down to topics relating to Cancer and, in certain cases, Bioinformatics, as a part of the same area of interest.
Stacey Gabriel focuses on Computational biology, Gene, Genetics, Whole genome sequencing and Genome. Her Computational biology study combines topics from a wide range of disciplines, such as Structural variation, Proteogenomics, Genomics, Population genetics and Proteomics. Stacey Gabriel has included themes like Epithelium and Embryo, Cell biology in her Gene study.
Genetics is often connected to Congenital hypoplastic anemia in her work. Her Whole genome sequencing research also works with subjects such as
Genetic architecture, which have a strong connection to Indel,
Precision medicine that connect with fields like Personalized medicine. Her Genome study also includes fields such as
Expression quantitative trait loci which is related to area like Evolutionary biology, Genetic genealogy, Heritability, Human genome and 1000 Genomes Project,
Chromothripsis, which have a strong connection to Mutation rate, Germline mutation, Germline, Point mutation and Massive parallel sequencing.
Her main research concerns Computational biology, Genomics, Genome, Proteogenomics and Proteomics. Her work in Computational biology addresses issues such as Genetic architecture, which are connected to fields such as Data sequences. Genomics is a subfield of Genetics that Stacey Gabriel explores.
Her Genome research incorporates themes from Chromothripsis, Population genetics and Genetic association. Her Proteogenomics study incorporates themes from Druggability, Histone, Serous fluid and Cancer research. Her Proteomics research includes elements of Cancer and Wnt signaling pathway.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
Aaron Henrik McKenna;Matthew Hanna;Eric Banks;Andrey Sivachenko.
Genome Research (2010)
EGFR mutations in lung cancer: correlation with clinical response to gefitinib therapy.
J. Guillermo Paez;Pasi A. Jänne;Pasi A. Jänne;Jeffrey C. Lee;Sean Tracy.
Science (2004)
A framework for variation discovery and genotyping using next-generation DNA sequencing data
Mark A DePristo;Eric Banks;Ryan Poplin;Kiran V Garimella.
Nature Genetics (2011)
Integrated Genomic Analysis Identifies Clinically Relevant Subtypes of Glioblastoma Characterized by Abnormalities in PDGFRA, IDH1, EGFR, and NF1
Roel G. W. Verhaak;Katherine A. Hoadley;Elizabeth Purdom;Victoria Wang.
Cancer Cell (2010)
Analysis of protein-coding genetic variation in 60,706 humans
Monkol Lek;Konrad J. Karczewski;Konrad J. Karczewski;Eric V. Minikel;Eric V. Minikel;Kaitlin E. Samocha.
Nature (2016)
Comprehensive molecular portraits of human breast tumours
Daniel C. Koboldt;Robert S. Fulton;Michael D. McLellan;Heather Schmidt.
Nature (2012)
A global reference for human genetic variation.
Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin.
Nature (2015)
The Structure of Haplotype Blocks in the Human Genome
Stacey B. Gabriel;Stephen F. Schaffner;Huy Nguyen;Jamie M. Moore.
Science (2002)
The Cancer Cell Line Encyclopedia enables predictive modelling of anticancer drug sensitivity
Jordi Barretina;Giordano Caponigro;Nicolas Stransky;Kavitha Venkatesan.
Nature (2012)
Comprehensive genomic characterization defines human glioblastoma genes and core pathways
Roger McLendon;Allan Friedman;Darrell Bigner;Erwin G. Van Meir.
Nature (2008)
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