Can Alkan spends much of his time researching Genetics, Genome, Human genome, Genomics and Evolutionary biology. He combines subjects such as Computational biology and Genetic diversity with his study of Genetics. His Computational biology research integrates issues from Genome-wide association study and 1000 Genomes Project.
His work deals with themes such as Neanderthal and Recent African origin of modern humans, which intersect with Genome. The Human genome study combines topics in areas such as Structural variation, Copy number analysis, Copy-number variation and DNA sequencing. His Genomics research includes elements of Population bottleneck and Reference genome.
The scientist’s investigation covers issues in Genetics, Genome, Computational biology, DNA sequencing and Genomics. In most of his Genetics studies, his work intersects topics such as Evolutionary biology. His study in Human genome, Reference genome, Segmental duplication, Whole genome sequencing and Genomic Structural Variation is done as part of Genome.
In Computational biology, Can Alkan works on issues like Hybrid genome assembly, which are connected to Exome sequencing and Personal genomics. His studies deal with areas such as Data mining and Sequence analysis as well as DNA sequencing. Can Alkan has included themes like Exome, Data science and Genetic variation in his Genomics study.
Can Alkan spends much of his time researching Genome, Computational biology, DNA sequencing, Genomics and Reference genome. His work in the fields of Genome, such as Genomic data, overlaps with other areas such as Set. His biological study spans a wide range of topics, including Structural variation, Segmental duplication, Whole genome sequencing, Germline and Ploidy.
His Structural variation research incorporates elements of Read depth, Gene conversion, Human genome and Human genetics. Can Alkan has researched Whole genome sequencing in several fields, including Exome sequencing, Copy Number Polymorphism, Copy-number variation, 1000 Genomes Project and GC-content. He undertakes interdisciplinary study in the fields of Genomics and Sequence assembly through his research.
His main research concerns Genome, Computational biology, Pipeline, Benchmark and Computer engineering. He works in the field of Genome, namely Genomics. His work carried out in the field of Genomics brings together such families of science as Organism, Structural variation, Human genome and Reference genome.
The study incorporates disciplines such as Personal Genome Project and Germline in addition to Benchmark. His Computer engineering research is multidisciplinary, incorporating elements of Dynamic programming, Filter and Speedup. His DNA sequencing research includes themes of Whole genome sequencing, Gene conversion and Segmental duplication.
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.
A global reference for human genetic variation.
Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin.
(2015)
A Draft Sequence of the Neandertal Genome
Richard E. Green;Johannes Krause;Adrian W. Briggs;Tomislav Maricic.
Science (2010)
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Alan E. Renton;Elisa Majounie;Adrian James Waite;Javier Simón-Sánchez;Javier Simón-Sánchez.
Neuron (2011)
Genetic history of an archaic hominin group from Denisova Cave in Siberia
David Reich;Richard E. Green;Martin Kircher;Johannes Krause.
Nature (2010)
An integrated map of structural variation in 2,504 human genomes
Peter H. Sudmant;Tobias Rausch;Eugene J. Gardner;Robert E. Handsaker;Robert E. Handsaker.
Nature (2015)
A high-coverage genome sequence from an archaic Denisovan individual
Matthias Meyer;Martin Kircher;Marie Theres Gansauge;Heng Li.
Science (2012)
Genome structural variation discovery and genotyping
Can Alkan;Bradley P. Coe;Evan E. Eichler;Evan E. Eichler.
Nature Reviews Genetics (2011)
Mapping and sequencing of structural variation from eight human genomes
Jeffrey M. Kidd;Gregory M. Cooper;William F. Donahue;Hillary S. Hayden.
Nature (2008)
Mapping copy number variation by population-scale genome sequencing
Ryan E. Mills;Klaudia Walter;Chip Stewart;Robert E. Handsaker.
(2011)
A global reference for human genetic variation
Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin.
(2015)
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