Fereydoun Hormozdiari
Molecular Biology · 2009–2017
A researcher in the Science corpus: 11 papers; trusts 1 researcher and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 138 citations into it; #13,608 of 17,773 by trust here, #1,089 by citations
Whom Fereydoun Hormozdiari trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Elaine R. Mardis
- Heng Li
- Jay Shendure
- Philip Green
- LaDeana W. Hillier
- Richard M. Karp
- Michael Olivier
- Jue Ruan
- Peter J. Campbell
- Mihai Pop
Who trusts Fereydoun Hormozdiari overall
Papers from Fereydoun Hormozdiari's perspective
Ordered by how strongly the researchers Fereydoun Hormozdiari trusts endorse each paper. Same corpus, a different order for every researcher.
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- The complete genome of an individual by massively parallel DNA sequencing (Nature)
- The Human Gene Mutation Database: 2008 update
- Exome sequencing as a tool for Mendelian disease gene discovery
- A framework for variation discovery and genotyping using next-generation DNA sequencing data
- [Structural variation in the human genome]. (Yi chuan = Hereditas)
- The Diploid Genome Sequence of an Individual Human (PLoS Biology)
- Identification of the transforming EML4–ALK fusion gene in non-small-cell lung cancer (Nature)
- Base-calling of automated sequencer traces using phred. II. Error probabilities.
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
Their papers
- Resolving the complexity of the human genome using single-molecule sequencing (2014) — 769 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- Personalized Copy-Number and Segmental Duplication Maps using Next-Generation Sequencing (2009) — 789 citations
- Multi-platform discovery of haplotype-resolved structural variation in human genomes (2017) — 796 citations
- mrsFast: a cache-oblivious algorithm for short-read mapping (2010) — 314 citations
- deFuse: An Algorithm for Gene Fusion Discovery in Tumor RNA-Seq Data (2011) — 562 citations
- Combinatorial Algorithms for Structural Variation Detection in High Throughput Sequenced Genomes (2009) — 331 citations
- An integrated map of structural variation in 2,504 human genomes (2015) — 2,247 citations
- Great ape genetic diversity and population history (2013) — 858 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations
- Mapping copy number variation by population scale genome sequencing (2011) — 1,130 citations