2019 - Fellow of the International Society for Computational Biology
Genetics, Genome, Genomics, Computational biology and Proteomics are his primary areas of study. The various areas that Vineet Bafna examines in his Genome study include Metaphase, Haplotype and DNA sequencing. His Genomics study incorporates themes from Genome-wide association study, Genetic variability, Genetic association, 1000 Genomes Project and Data set.
His study in Computational biology is interdisciplinary in nature, drawing from both Shotgun sequencing, Bioinformatics, Protein family, Base pair and Sequence. The study incorporates disciplines such as Genome evolution, Genome project, Gene density, Genome size and Nonsynonymous substitution in addition to Reference genome. His Gene density research is multidisciplinary, incorporating perspectives in Sequence-tagged site and Hybrid genome assembly.
The scientist’s investigation covers issues in Computational biology, Genetics, Genome, Genomics and Haplotype. His Computational biology research incorporates themes from Structural variation, Bioinformatics, Proteomics, Sequence and Mass spectrometry. His work deals with themes such as Proteogenomics and Gene prediction, which intersect with Proteomics.
His research related to Human genome, Gene, DNA sequencing, Genome-wide association study and Allele might be considered part of Genetics. Vineet Bafna has included themes like Proteome, Data mining and Human genetics in his Genome study. His Haplotype research is multidisciplinary, relying on both Evolutionary biology and Single-nucleotide polymorphism.
His primary areas of investigation include Computational biology, Genome, Extrachromosomal DNA, Cancer and Cancer research. His Computational biology research is multidisciplinary, incorporating elements of Genomics, Optical mapping, Human genetics and Human genome. His biological study spans a wide range of topics, including Data mining and Identification.
His Cancer research includes themes of Amplicon and Whole genome sequencing. His Gene study contributes to a more complete understanding of Genetics. His Genetics study frequently draws connections to other fields, such as Pathogenesis.
His main research concerns Computational biology, Extrachromosomal DNA, Genome, Cancer and Cancer research. His studies in Computational biology integrate themes in fields like Metaproteomics, Tandem mass spectrum, Underlying disease and Genomics. His research in Genomics intersects with topics in Nucleic acid amplification technique, Selection, Selective sweep and Population genetics.
Vineet Bafna interconnects Transcription, Human genetics and Intratumoral Genetic Heterogeneity in the investigation of issues within Extrachromosomal DNA. His Genome study combines topics from a wide range of disciplines, such as Identification and DNA barcoding. His work carried out in the field of DNA barcoding brings together such families of science as Identification, DNA sequencing, Reference genome, Environmental DNA and Sample.
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The sequence of the human genome.
J. Craig Venter;Mark D. Adams;Eugene W. Myers;Peter W. Li.
Science (2001)
A global reference for human genetic variation.
Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin.
(2015)
The Diploid Genome Sequence of an Individual Human
Samuel Levy;Granger Sutton;Pauline C Ng;Lars Feuk.
PLOS Biology (2007)
A global reference for human genetic variation
Adam Auton;Gonçalo R. Abecasis;David M. Altshuler;Richard M. Durbin.
PMC (2015)
The Sorcerer II Global Ocean Sampling expedition: expanding the universe of protein families.
Shibu Yooseph;Granger Sutton;Douglas B. Rusch;Aaron L Halpern.
PLOS Biology (2007)
Human beta-defensin 2 is a salt-sensitive peptide antibiotic expressed in human lung
R. Bals;Xiaorong Wang;Zhongren Wu;T. Freeman.
Journal of Clinical Investigation (1998)
InsPecT: identification of posttranslationally modified peptides from tandem mass spectra.
Stephen Tanner;Hongjun Shu;Ari Frank;Ling-Chi Wang.
Analytical Chemistry (2005)
Genome Rearrangements and Sorting by Reversals
Vineet Bafna;Pavel A. Pevzner.
SIAM Journal on Computing (1996)
Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding
Kevin Judd McKernan;Heather E. Peckham;Gina L. Costa;Stephen F. McLaughlin.
Genome Research (2009)
The dog genome: Survey sequencing and comparative analysis
Ewen F. Kirkness;Vineet Bafna;Aaron L. Halpern;Samuel Levy.
Science (2003)
Algorithms for Molecular Biology
(Impact Factor: 1.721)
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