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Bud Mishra

Researcher at New York University

Publications -  225
Citations -  4424

Bud Mishra is an academic researcher from New York University. The author has contributed to research in topics: Temporal logic & Model checking. The author has an hindex of 32, co-authored 222 publications receiving 4079 citations. Previous affiliations of Bud Mishra include University of Wisconsin-Madison & Watson School of Biological Sciences.

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Automated high resolution optical mapping using arrayed, fluid-fixed DNA molecules

TL;DR: The aggregate significance of this work is the development of an integrated system for mapping small insert clones allowing biochemical data obtained from engineered ensembles of individual molecules to be automatically accumulated and analyzed for map construction.
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Whole-genome shotgun optical mapping of Deinococcus radiodurans.

TL;DR: A whole-genome restriction map of Deinococcus radiodurans, a radiation-resistant bacterium able to survive up to 15,000 grays of ionizing radiation, was constructed without using DNA libraries, the polymerase chain reaction, or electrophoresis.
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Comparing de novo genome assembly: the long and short of it.

TL;DR: This paper highlights common anomalies in assembly accuracy through a rigorous study of several assemblers, compared under both standard metrics as well as a more comprehensive metric (Feature-Response Curves, FRC) that is introduced here; FRC transparently captures the trade-offs between contigs' quality against their sizes.
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Model building and model checking for biochemical processes.

TL;DR: A novel computational tool is described that achieves many of the goals of this new discipline of computational systems biology and involves an automaton-based semantics of the temporal evolution of complex biochemical reactions starting from the representation given as a set of differential equations.
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Distinct Classes of Complex Structural Variation Uncovered across Thousands of Cancer Genome Graphs.

TL;DR: Clustering of tumors according to genome graph-derived features identified subgroups associated with DNA repair defects and poor prognosis and uncovered three novel complex rearrangement phenomena: pyrgo, rigma, and tyfonas.