2020 - Fellow of the International Society for Computational Biology
Member of the European Molecular Biology Organization (EMBO)
Genetics, Genome, Computational biology, Genomics and Human genome are his primary areas of study. His Gene, Epigenomics, Genetic variation, Genome-wide association study and Chromatin immunoprecipitation study are his primary interests in Genetics. His Genome research includes elements of Evolutionary biology and Enhancer.
The various areas that he examines in his Computational biology study include Annotation, Reference genome, Ensembl, 1000 Genomes Project and Molecular Sequence Annotation. His Genomics study incorporates themes from Sequence analysis, Whole genome sequencing and Systems biology. His Human genome research includes themes of Genome evolution, ENCODE, Chromatin, Expression quantitative trait loci and DNA sequencing.
Paul Flicek mostly deals with Genetics, Genome, Computational biology, Gene and Genomics. His biological study spans a wide range of topics, including Evolutionary biology and DNA sequencing. His study on Evolutionary biology also encompasses disciplines like
Paul Flicek has included themes like Annotation, Transcriptome, Genotyping, Ensembl and Sequence in his Computational biology study. His Ensembl research incorporates themes from Genome browser, Comparative genomics, World Wide Web, Gene Annotation and Molecular Sequence Annotation. His Genomics study combines topics from a wide range of disciplines, such as Genome project, Genome-wide association study, Data science and 1000 Genomes Project.
His scientific interests lie mostly in Genome, Gene, Computational biology, Evolutionary biology and Genomics. He usually deals with Genome and limits it to topics linked to Annotation and Genome browser. His Gene study is concerned with the field of Genetics as a whole.
Paul Flicek merges Genetics with Ribosomal protein in his research. The Computational biology study combines topics in areas such as Human genome, Whole genome sequencing, Expression quantitative trait loci, Genotyping and Haplotype. As part of one scientific family, he deals mainly with the area of Genomics, narrowing it down to issues related to the 1000 Genomes Project, and often Indel.
Paul Flicek mainly investigates Computational biology, Genome, Genomics, Gene and Human genome. Computational biology is frequently linked to Sequence assembly in his study. The concepts of his Genome study are interwoven with issues in Evolutionary biology, Genetic linkage, DNA sequencing and 1000 Genomes Project.
Paul Flicek combines subjects such as Annotation, Whole genome sequencing and Reference genome with his study of Genomics. His work on Human genomics as part of general Human genome research is frequently linked to Declaration, thereby connecting diverse disciplines of science. His Spliceosome research entails a greater understanding of Genetics.
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.
Initial sequencing and comparative analysis of the mouse genome.
Robert H. Waterston;Kerstin Lindblad-Toh;Ewan Birney;Jane Rogers.
Nature (2002)
A global reference for human genetic variation.
Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin.
Nature (2015)
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
Ewan Birney;John A. Stamatoyannopoulos;Anindya Dutta;Roderic Guigó.
Nature (2007)
An integrated encyclopedia of DNA elements in the human genome
Ian Dunham;Anshul Kundaje;Shelley F. Aldred;Patrick J. Collins.
PMC (2012)
The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
Danielle Welter;Jacqueline A. L. MacArthur;Joannella Morales;Tony Burdett.
Nucleic Acids Research (2014)
The Ensembl Variant Effect Predictor.
William McLaren;Laurent Gil;Sarah E. Hunt;Harpreet Singh Riat.
Genome Biology (2016)
Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution
Ladeana W. Hillier;Webb Miller;Ewan Birney;Wesley Warren.
Nature (2004)
Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor
William McLaren;Bethan Pritchard;Daniel Rios;Yuan Chen.
Bioinformatics (2010)
The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog).
Jacqueline A. L. MacArthur;Emily Bowler;Maria Cerezo;Laurent Gil.
Nucleic Acids Research (2017)
The IPD and IMGT/HLA database: allele variant databases
James Robinson;Jason A. Halliwell;James D. Hayhurst;Paul Flicek.
Nucleic Acids Research (2015)
Profile was last updated on December 6th, 2021.
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