Can Alkan
Genetics · 2008–2020
A researcher in the Science corpus: 18 papers; trusts 8 researchers and is trusted by 5 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 262 citations into it; #2,401 of 6,854 by trust here, #47 by citations
- Molecular Biology — 246 citations into it; #7,024 of 17,773 by trust here, #887 by citations
Whom Can Alkan trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Mark J. P. Chaisson
- Zheng Zhang
- Elaine R. Mardis
- Ryan E. Mills
- Jerzy Jurka
- Peter J. Campbell
- Heng Li
- Michael C. Schatz
- Dumitru Brinza
- Pavel A. Pevzner
Who trusts Can Alkan overall
- Computational Pan-Genomics Consortium
- Todd J. Treangen
- Min Zhao
- Daniel C. Koboldt
- Heng Li
- Steven L. Salzberg
- Ruibang Luo
- Ryan M. Layer
- Davide Heller
- Colby Chiang
Papers from Can Alkan's perspective
Ordered by how strongly the researchers Can Alkan trusts endorse each paper. Same corpus, a different order for every researcher.
- Accurate Whole Human Genome Sequencing using Reversible Terminator Chemistry (Nature)
- Common deletion polymorphisms in the human genome (Nature Genetics)
- Genome sequencing in microfabricated high-density picolitre reactors (Nature)
- The Diploid Genome Sequence of an Individual Human (PLoS Biology)
- [Structural variation in the human genome]. (Yi chuan = Hereditas)
- The Human Gene Mutation Database: 2008 update
- Exome sequencing as a tool for Mendelian disease gene discovery
- Large-Scale Copy Number Polymorphism in the Human Genome (Science)
- Substantial biases in ultra-short read data sets from high-throughput DNA sequencing (Nucleic Acids Research)
- Phenotypic impact of genomic structural variation: insights from and for human disease (Nature reviews genetics)
Their papers
- Limitations of next-generation genome sequence assembly (2010) — 742 citations
- A global reference for human genetic variation (2015) — 16,925 citations
- Diversity of Human Copy Number Variation and Multicopy Genes (2010) — 724 citations
- Mapping and sequencing of structural variation from eight human genomes (2008) — 1,208 citations
- Genome structural variation discovery and genotyping (2011) — 1,575 citations
- mrsFast: a cache-oblivious algorithm for short-read mapping (2010) — 314 citations
- A robust benchmark for detection of germline large deletions and insertions (2020) — 358 citations
- Combinatorial Algorithms for Structural Variation Detection in High Throughput Sequenced Genomes (2009) — 331 citations
- Insights into hominid evolution from the gorilla genome sequence (2012) — 719 citations
- Comparative and demographic analysis of orangutan genomes (2011) — 595 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
- A HIGH COVERAGE GENOME SEQUENCE FROM AN ARCHAIC DENISOVAN INDIVIDUAL (2012) — 1,845 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
- A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD (2011) — 4,318 citations
- Genetic history of an archaic hominin group from Denisova Cave in Siberia (2010) — 1,704 citations
- A Draft Sequence of the Neandertal Genome (2010) — 3,888 citations