Paul Flicek
Molecular Biology · 2001–2022
A researcher in the Science corpus: 84 papers; trusts 15 researchers and is trusted by 15 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 1,526 citations into it; #3,341 of 17,773 by trust here, #35 by citations
- Genetics — 758 citations into it; #6,640 of 6,854 by trust here, #24 by citations
- Plant Science — 334 citations into it
- Artificial Intelligence — 69 citations into it
Whom Paul Flicek trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Kim D. Pruitt
- J. Harrow
- Jason Ernst
- J. Ashurst
- Axel Visel
- Benedict Paten
- Donna R. Maglott
- Tatiana A. Tatusova
- Albert J. Vilella
- Val Curwen
Who trusts Paul Flicek overall
- Mario Stanke
- The UniProt Consortium
- Christoph Bock
- Robert M. Kuhn
- Mark Yandell
- Ivica Letunic
- Lincoln D. Stein
- Stephan Waack
- Steven L. Salzberg
- Bo Li
Papers from Paul Flicek's perspective
Ordered by how strongly the researchers Paul Flicek trusts endorse each paper. Same corpus, a different order for every researcher.
- dbSNP: the NCBI database of genetic variation
- NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins (Nucleic Acids Res.)
- Enredo and Pecan: genome-wide mammalian consistency-based multiple alignment with paralogs. (Genome Research)
- NCBI Reference Sequences: current status, policy and new initiatives (Nucleic Acids Res.)
- Ensembl’s 10th year (Nucleic Acids Res.)
- Human-mouse alignments with BLASTZ. (Genome Research)
- GENCODE: producing a reference annotation for ENCODE (Genome Biology)
- Transcriptional regulatory elements in the human genome. (Annual review of genomics and human genetics (Print))
- The Pfam protein families database
- The Distributed Annotation System (BMC Bioinformatics)
Their papers
- EGASP: the human ENCODE Genome Annotation Assessment Project (2006) — 351 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) — 5,374 citations
- Ensembl’s 10th year (2009) — 318 citations
- Bioinformatics Applications Note Databases and Ontologies Deriving the Consequences of Genomic Variants with the Ensembl Api and Snp Effect Predictor — 1,610 citations
- The Ensembl gene annotation system (2016) — 1,134 citations
- The Ensembl Variant Effect Predictor (2016) — 7,148 citations
- Integrating genomic homology into gene structure prediction (2001) — 510 citations
- De novo assembly and genotyping of variants using colored de Bruijn graphs (2012) — 677 citations
- Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly (2016) — 1,005 citations
- Multi-platform discovery of haplotype-resolved structural variation in human genomes (2017) — 796 citations
- Ensembl 2007 (2006) — 531 citations
- Transcriptome and genome sequencing uncovers functional variation in humans (2013) — 2,017 citations
- A Bayesian deconvolution strategy for immunoprecipitation-based DNA methylome analysis (2008) — 669 citations
- Ensembl 2011 (2010) — 480 citations
- Ensembl 2012 (2011) — 647 citations
- Ensembl 2009 (2008) — 549 citations
- The Ensembl Regulatory Build (2015) — 400 citations
- The NHGRI GWAS Catalog, a curated resource of SNP-trait associations (2013) — 2,838 citations
- Initial sequencing and comparative analysis of the mouse genome. (2002) — 4,291 citations