Noah A. Rosenberg | |
---|---|
Alma mater | Rice University |
Spouse(s) | Donna Zulman, MD |
Awards | Fellow of the American Association for the Advancement of Science |
Scientific career | |
Fields | Population genetics Phylogenetics Mathematical and theoretical biology |
Thesis | Statistical modeling of genetic histories and relationships of populations (2001) |
Doctoral advisor | Marcus Feldman [1] |
Website | rosenberglab |
Noah Aubrey Rosenberg is a geneticist working in evolutionary biology, mathematical phylogenetics, and population genetics, and is the Stanford Professor of Population Genetics and Society. [2] His research focuses on mathematical modeling and statistical methods for genetics and evolution [3] and he is the editor-in-chief of Theoretical Population Biology . [4]
Rosenberg graduated from the Illinois Mathematics and Science Academy in 1993, where he began the mathematical reference known as The Noah Sheets. [5] He earned a BA in mathematics from Rice University in 1997, where he scored among the top 100 students in the Putnam Competition. [6] Rosenberg earned an MS in mathematics from Stanford University in 1999 and a PhD in biology from Stanford University in 2001 under the supervision of Marcus Feldman. [7] His dissertation was titled "Statistical modeling of genetic histories and relationships of populations." [8] Part of his dissertation work was recognized as The Lancet's 2003 paper of the year. [9] From 2001 to 2005, Rosenberg was a postdoctoral fellow at the University of Southern California. [7]
Rosenberg was a professor at the University of Michigan from 2005 to 2011, where he held appointments in the Department of Human Genetics, the Department of Ecology and Evolutionary Biology, and the Department of Biostatistics. He joined the Stanford University Department of Biology as an associate professor in 2011 and was promoted to full professor in 2014, when he was named the Stanford Professor of Population Genetics and Society. [2] He is a member of Stanford's Institute for Computational and Mathematical Engineering (ICME) and Stanford Bio-X. [10] [11] Rosenberg was elected as a fellow of the American Association for the Advancement of Science in 2018. [12]
Rosenberg has published more than 150 peer-reviewed articles and has advised more than 35 doctoral students and postdoctoral fellows. [6] His trainees have gone on to professorships at universities including Cornell University, [13] Duke University, [14] the MD Anderson Cancer Center, [15] and the University of Southern California. [16] [17]
Rosenberg has served as the editor-in-chief of the journal Theoretical Population Biology since 2013 [4] and has served as an associate editor for scientific journals including Genetics and Evolution, Medicine, and Public Health. [18] He is also a co-director of the Stanford Center for Computational, Evolutionary, and Human Genomics. [19] In 2018, Rosenberg started the Stanford X-Tree Project, a website illustrating concepts from phylogenetics using photographs of real trees from the Stanford campus. [20]
Much of Rosenberg's work has analyzed global patterns of genetic and linguistic variation, [9] [21] [22] [23] including developing software for the analysis and visualization of population ancestry data. [24] [25] [ non-primary source needed ] He has also studied the genetic histories of specific people groups, such as the Ohlone Indigenous population of California, [26] African Americans, [27] and Jewish populations. [28]
Rosenberg's work in forensic genetics has explored the implications of imputation techniques for genetic privacy. [29] [30] His work in coalescent theory has characterized the effects of consanguinity, [31] founder events, [32] and migration [33] on patterns of genetic variation. And his work in human genetics has investigated the implications of population history for association studies and polygenic scores. [34] [35]
Rosenberg has contributed to the understanding of mathematical properties of objects and quantities used in evolutionary biology. His work includes combinatorial enumeration of phylogenetic trees and coalescent histories, [36] [37] [38] [39] analysis of evolutionary models, [40] [41] [42] and derivation of mathematical bounds on population-genetic statistics. [43] [44] [45] He has also applied population-genetic statistics to other fields, such as his 2020 paper bridging health care efficiency research and population-genetic statistics which he co-authored with his wife, Donna Zulman. [46]
Rosenberg is a regular contributor to the On-Line Encyclopedia of Integer Sequences. [47] [48] [49]
Bioinformatics is an interdisciplinary field of science that develops methods and software tools for understanding biological data, especially when the data sets are large and complex. Bioinformatics uses biology, chemistry, physics, computer science, computer programming, information engineering, mathematics and statistics to analyze and interpret biological data. The subsequent process of analyzing and interpreting data is referred to as computational biology.
In biology, phylogenetics is the study of the evolutionary history and relationships among or within groups of organisms. These relationships are determined by phylogenetic inference, methods that focus on observed heritable traits, such as DNA sequences, protein amino acid sequences, or morphology. The result of such an analysis is a phylogenetic tree—a diagram containing a hypothesis of relationships that reflects the evolutionary history of a group of organisms.
In human genetics, the Mitochondrial Eve is the matrilineal most recent common ancestor (MRCA) of all living humans. In other words, she is defined as the most recent woman from whom all living humans descend in an unbroken line purely through their mothers and through the mothers of those mothers, back until all lines converge on one woman.
A phylogenetic tree, phylogeny or evolutionary tree is a graphical representation which shows the evolutionary history between a set of species or taxa during a specific time. In other words, it is a branching diagram or a tree showing the evolutionary relationships among various biological species or other entities based upon similarities and differences in their physical or genetic characteristics. In evolutionary biology, all life on Earth is theoretically part of a single phylogenetic tree, indicating common ancestry. Phylogenetics is the study of phylogenetic trees. The main challenge is to find a phylogenetic tree representing optimal evolutionary ancestry between a set of species or taxa. Computational phylogenetics focuses on the algorithms involved in finding optimal phylogenetic tree in the phylogenetic landscape.
Computational biology refers to the use of data analysis, mathematical modeling and computational simulations to understand biological systems and relationships. An intersection of computer science, biology, and big data, the field also has foundations in applied mathematics, chemistry, and genetics. It differs from biological computing, a subfield of computer science and engineering which uses bioengineering to build computers.
Population genetics is a subfield of genetics that deals with genetic differences within and among populations, and is a part of evolutionary biology. Studies in this branch of biology examine such phenomena as adaptation, speciation, and population structure.
Mathematical and theoretical biology, or biomathematics, is a branch of biology which employs theoretical analysis, mathematical models and abstractions of living organisms to investigate the principles that govern the structure, development and behavior of the systems, as opposed to experimental biology which deals with the conduction of experiments to test scientific theories. The field is sometimes called mathematical biology or biomathematics to stress the mathematical side, or theoretical biology to stress the biological side. Theoretical biology focuses more on the development of theoretical principles for biology while mathematical biology focuses on the use of mathematical tools to study biological systems, even though the two terms are sometimes interchanged.
In biology and genetic genealogy, the most recent common ancestor (MRCA), also known as the last common ancestor (LCA), of a set of organisms is the most recent individual from which all the organisms of the set are descended. The term is also used in reference to the ancestry of groups of genes (haplotypes) rather than organisms.
Coalescent theory is a model of how alleles sampled from a population may have originated from a common ancestor. In the simplest case, coalescent theory assumes no recombination, no natural selection, and no gene flow or population structure, meaning that each variant is equally likely to have been passed from one generation to the next. The model looks backward in time, merging alleles into a single ancestral copy according to a random process in coalescence events. Under this model, the expected time between successive coalescence events increases almost exponentially back in time. Variance in the model comes from both the random passing of alleles from one generation to the next, and the random occurrence of mutations in these alleles.
Masatoshi Nei was a Japanese-born American evolutionary biologist.
Population structure is the presence of a systematic difference in allele frequencies between subpopulations. In a randomly mating population, allele frequencies are expected to be roughly similar between groups. However, mating tends to be non-random to some degree, causing structure to arise. For example, a barrier like a river can separate two groups of the same species and make it difficult for potential mates to cross; if a mutation occurs, over many generations it can spread and become common in one subpopulation while being completely absent in the other.
Genetic admixture occurs when previously isolated populations interbreed resulting in a population that is descended from multiple sources. It can occur between species, such as with hybrids, or within species, such as when geographically distant individuals migrate to new regions. It results in gene pool that is a mix of the source populations.
A genetic lineage includes all descendants of a given genetic sequence, typically following a new mutation. It is not the same as an allele because it excludes cases where different mutations give rise to the same allele, and includes descendants that differ from the ancestor by one or more mutations. The genetic sequence can be of different sizes, e.g. a single gene or a haplotype containing multiple adjacent genes along a chromosome. Given recombination, each gene can have a separate genetic lineages, even as the population shares a single organismal lineage. In asexual microbes or somatic cells, cell lineages exactly match genetic lineages, and can be traced.
Ziheng Yang FRS is a Chinese biologist. He holds the R.A. Fisher Chair of Statistical Genetics at University College London, and is the Director of R.A. Fisher Centre for Computational Biology at UCL. He was elected a Fellow of the Royal Society in 2006.
Jonathan Karl Pritchard is an English-born professor of genetics at Stanford University, best known for his development of the STRUCTURE algorithm for studying population structure and his work on human genetic variation and evolution. His research interests lie in the study of human evolution, in particular in understanding the association between genetic variation among human individuals and human traits.
Incomplete lineage sorting, also termed hemiplasy, deep coalescence, retention of ancestral polymorphism, or trans-species polymorphism, describes a phenomenon in population genetics when ancestral gene copies fail to coalesce into a common ancestral copy until deeper than previous speciation events. It is caused by lineage sorting of genetic polymorphisms that were retained across successive nodes in the species tree. In other words, the tree produced by a single gene differs from the population or species level tree, producing a discordant tree. Whatever the mechanism, the result is that a generated species level tree may differ depending on the selected genes used for assessment. This is in contrast to complete lineage sorting, where the tree produced by the gene is the same as the population or species level tree. Both are common results in phylogenetic analysis, although it depends on the gene, organism, and sampling technique.
Viral phylodynamics is the study of how epidemiological, immunological, and evolutionary processes act and potentially interact to shape viral phylogenies. Since the term was coined in 2004, research on viral phylodynamics has focused on transmission dynamics in an effort to shed light on how these dynamics impact viral genetic variation. Transmission dynamics can be considered at the level of cells within an infected host, individual hosts within a population, or entire populations of hosts.
Marcus William Feldman is the Burnet C. and Mildred Finley Wohlford Professor of Biological Sciences, director of the Morrison Institute for Population and Resource Studies, and co-director of the Center for Computational, Evolutionary and Human Genomics (CEHG) at Stanford University. He is an Australian-born mathematician turned American theoretical biologist, best known for his mathematical evolutionary theory and computational studies in evolutionary biology, and for originating with L. L. Cavalli-Sforza the theory of cultural evolution.
Multispecies Coalescent Process is a stochastic process model that describes the genealogical relationships for a sample of DNA sequences taken from several species. It represents the application of coalescent theory to the case of multiple species. The multispecies coalescent results in cases where the relationships among species for an individual gene can differ from the broader history of the species. It has important implications for the theory and practice of phylogenetics and for understanding genome evolution.
Sohini Ramachandran is professor at Brown University known for her work in evolutionary biology and population genetics.
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