James C. Mullikin mainly focuses on Genetics, Genome, Human genome, Genomics and Evolutionary biology. His research combines Computational biology and Genome. His Computational biology research incorporates elements of Genome evolution, Functional genomics, GENCODE, Hybrid genome assembly and DNase-Seq.
His studies in Hybrid genome assembly integrate themes in fields like DNA sequencing theory and Cancer genome sequencing. The study incorporates disciplines such as Structural variation, Recent African origin of modern humans, ENCODE, Reference genome and Exome in addition to Human genome. His Genomics research is multidisciplinary, relying on both Lineage and Systems biology.
His primary scientific interests are in Genetics, Genome, Gene, Exome sequencing and Human genome. His research links Computational biology with Genetics. His Computational biology research is multidisciplinary, incorporating perspectives in Sequence alignment, DNA microarray, Hybrid genome assembly, RNA splicing and Sequence.
His studies link Evolutionary biology with Genome. His work focuses on many connections between Exome sequencing and other disciplines, such as Germline mutation, that overlap with his field of interest in Molecular biology. His research on Human genome frequently connects to adjacent areas such as Structural variation.
Genetics, Genome, Gene, Computational biology and Exome sequencing are his primary areas of study. His research in Genetics focuses on subjects like Age of onset, which are connected to Trinucleotide repeat expansion. James C. Mullikin has researched Genome in several fields, including Evolutionary biology and Sequence analysis.
His study on Genome evolution, Synteny, Gene duplication and Comparative genomics is often connected to Common goldfish as part of broader study in Gene. James C. Mullikin interconnects Human genome, Pseudoautosomal region, Nanopore sequencing, Reference genome and Telomere assembly in the investigation of issues within Computational biology. His studies deal with areas such as Genetic counseling and Genetic variation as well as Exome sequencing.
James C. Mullikin mostly deals with Genome, Computational biology, Telomere assembly, Nanopore sequencing and Reference genome. The study of Genome is intertwined with the study of Sequence assembly in a number of ways. His Computational biology research is multidisciplinary, incorporating elements of Personal Genome Project and Germline.
James C. Mullikin combines subjects such as Manual curation, Base pair, DNA, Concordance and Structural variant with his study of Germline. The Telomere assembly study combines topics in areas such as Human genome, Pseudoautosomal region, X chromosome, Human genetics and Tandem repeat. His study brings together the fields of Segmental duplication and Nanopore sequencing.
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Initial sequencing and analysis of the human genome.
Eric S. Lander;Lauren M. Linton;Bruce Birren;Chad Nusbaum.
Nature (2001)
Initial sequencing and comparative analysis of the mouse genome.
Robert H. Waterston;Kerstin Lindblad-Toh;Ewan Birney;Jane Rogers.
Nature (2002)
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)
The International HapMap Project
John W. Belmont;Paul Hardenbol;Thomas D. Willis;Fuli Yu.
(2003)
A haplotype map of the human genome
John W. Belmont;Andrew Boudreau;Suzanne M. Leal;Paul Hardenbol.
(2005)
A second generation human haplotype map of over 3.1 million SNPs
Kelly A. Frazer;Dennis G. Ballinger;David R. Cox;David A. Hinds.
(2007)
Accurate whole human genome sequencing using reversible terminator chemistry
David R. Bentley;Shankar Balasubramanian;Harold P. Swerdlow;Harold P. Swerdlow;Geoffrey P. Smith.
Nature (2008)
A Draft Sequence of the Neandertal Genome
Richard E. Green;Johannes Krause;Adrian W. Briggs;Tomislav Maricic.
Science (2010)
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
Ravi Sachidanandam;David Weissman;Steven C. Schmidt;Jerzy M. Kakol.
Nature (2001)
Genome-wide detection and characterization of positive selection in human populations
Pardis C. Sabeti;Pardis C. Sabeti;Patrick Varilly;Patrick Varilly;Ben Fry;Jason Lohmueller.
(2007)
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