C
Carlos Bustamante
Researcher at Stanford University
Publications - 799
Citations - 122303
Carlos Bustamante is an academic researcher from Stanford University. The author has contributed to research in topics: Population & DNA. The author has an hindex of 161, co-authored 770 publications receiving 106053 citations. Previous affiliations of Carlos Bustamante include Lawrence Berkeley National Laboratory & University of California.
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Journal ArticleDOI
Directional selection and the site-frequency spectrum.
TL;DR: The power of the likelihood ratio tests (LRT) of neutrality for varying levels of mutation and selection as well as the robustness of the LRT to deviations from the assumption of free recombination among sites are explored.
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Genetic recombination is targeted towards gene promoter regions in dogs.
Adam Auton,Yingrui Li,Jeffrey M. Kidd,Kyle C. Oliveira,Julie Nadel,J. Kim Holloway,Jessica J. Hayward,Paula E. Cohen,John M. Greally,Jun Wang,Carlos Bustamante,Adam R. Boyko +11 more
TL;DR: A fine-scale genetic map is constructed from patterns of linkage disequilibrium assessed using high-throughput sequence data from 51 free-ranging dogs to show that biased gene conversion is a plausible mechanism by which the high CpG content of the dog genome could have occurred.
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Development of genome-wide SNP assays for rice
Susan R. McCouch,Keyan Zhao,Keyan Zhao,Mark G. Wright,Chih-Wei Tung,Kaworu Ebana,Michael J. Thomson,Andrew R. Reynolds,Diane R. Wang,Genevieve DeClerck,Md. Liakat Ali,Anna M. McClung,Georgia C. Eizenga,Carlos Bustamante,Carlos Bustamante +14 more
TL;DR: A suite of SNP-based resources have been developed and made publicly available for broad application in rice research, including large SNP datasets, tools for identifying informative SNPs for targeted applications, and a suite of custom-designed SNP assays for use in marker-assisted and genomic selection, association and QTL mapping, positional cloning, pedigree analysis, variety identification and seed purity testing as mentioned in this paper.
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Replication of mitochondrial DNA occurs by strand displacement with alternative light-strand origins, not via a strand-coupled mechanism
TL;DR: Examination of mtDNA replicative intermediates from mouse liver using atomic force microscopy and 2D agarose gel electrophoresis provides evidence for only the orthodox, strand-displacement mode of replication and reveals the presence of additional, alternative origins of lagging light-strand mtDNA synthesis.
Journal ArticleDOI
Mechanical force releases nascent chain–mediated ribosome arrest in vitro and in vivo
Daniel Goldman,Christian M. Kaiser,Christian M. Kaiser,Anthony Milin,Anthony Milin,Maurizio Righini,Ignacio Tinoco,Carlos Bustamante +7 more
TL;DR: A kinetic model is formulated describing how a protein can regulate its own synthesis by the force generated during folding, tuning ribosome activity to structure acquisition by a nascent polypeptide.