Dilepton-jet final states are used to study physical phenomena not predicted by the standard model. The ATLAS discovery potential for leptoquarks and Majorana Neutrinos is presented using a full...
The diploid genome sequence of an individual human (2008)
Samuel Levy, Granger Sutton, Pauline C. Ng, Lars Feuk, Aaron L. Halpern, Brian P. Walenz, ...
Presented here is a genome sequence of an individual human. It was produced from;32 million random DNA fragments, sequenced by Sanger dideoxy technology and assembled into 4,528 scaffolds, comprising...
Running Head: A Decomposition Theory for Phylogenetic Networks ∗ Corresponding Author: (2008)
Dan Gusfield, Vikas Bansal, Vineet Bafna, Yun S. Song, Dan Gusfield
1 Phylogenetic networks are models of evolution that go beyond trees, incorporating non-tree-like biological events such as recombination (or more generally reticulation), which occur either in a...
The Number of Recombination Events in a Sample History: Conflict Graph (2008)
Lower Bounds, Vineet Bafna, Vikas Bansal
Abstract—We consider the following problem: Given a set of binary sequences, determine lower bounds on the minimum number of recombinations required to explain the history of the sample, under the...
Search for Leptoquarks, Excited Leptons and Technicolor at the LHC (2008)
The ATLAS and CMS experiments at the Large Hadron Collider (LHC) will soon search for physics phenomena that are not predicted by the Standard Model. Technicolor, Compositeness and GUT-based models...
Area —— Model, Design and Construction of a Service-Oriented (2008)
Contact Gregory Cobena, Inria Rocquencourt, Serge Abiteboul, Vikas Bansal, Gregory Cobena, Benjamin Nguyen, ...
We propose a new methodology, a language and tools for the design and construction of Web data warehouses. Our approach is Service Oriented, in that our framework makes an extensive use of Web...
The diploid genome sequence of an individual human (2008)
Samuel Levy, Granger Sutton, Pauline C. Ng, Lars Feuk, Aaron L. Halpern, Brian P. Walenz, ...
Presented here is a genome sequence of an individual human. It was produced from;32 million random DNA fragments, sequenced by Sanger dideoxy technology and assembled into 4,528 scaffolds, comprising...
An MCMC algorithm for haplotype assembly from whole-genome sequence data (2008)
Bansal, Vikas, Halpern, Aaron L., Axelrod, Nelson, Bafna, Vineet
In comparison to genotypes, knowledge about haplotypes (the combination of alleles present on a single chromosome) is much more useful for whole-genome association studies and for making inferences...
The Diploid Genome Sequence of an Individual Human (2007)
Samuel Levy, Granger Sutton, Pauline C. Ng, Lars Feuk, Aaron L. Halpern, Brian P. Walenz, ...
Presented here is a genome sequence of an individual human. It was produced from ∼32 million random DNA fragments, sequenced by Sanger dideoxy technology and assembled into 4,528 scaffolds,...
Evidence for large inversion polymorphisms in the human genome from HapMap data (2006)
Bansal, Vikas, Bashir, Ali, Bafna, Vineet
Knowledge about structural variation in the human genome has grown tremendously in the past few years. However, inversions represent a class of structural variation that remains difficult to detect....
Improved recombination lower bounds for haplotype data (2005)
ABSTRACT Recombination is an important evolutionary mechanism responsible for the genetic diversity in humans and other organisms. Recently, there has been extensive research on understanding the...
Post Genomic Algorithms (CSE 291A) (2003)
We start by giving a brief biological background. DNA is one of the most important biological molecules. It is a large molecule composed of four basic units called nucleotides. Each nucleotide is...
A simple method for interactive 3D reconstruction and camera calibration from a single view (2002)
Akash M Kushal, Vikas Bansal, Subhashis Banerjee
single view
A simple method for interactive 3D reconstruction and camera calibration from a single view (2002)
Akash M Kushal, Vikas Bansal, Subhashis Banerjee
single view
Evidence for large inversion polymorphisms in the human genome from HapMap data
Bansal, Vikas, Bashir, Ali, Bafna, Vineet
Knowledge about structural variation in the human genome has grown tremendously in the past few years. However, inversions represent a class of structural variation that remains difficult to detect....
The Diploid Genome Sequence of an Individual Human
Levy, Samuel, Sutton, Granger, Ng, Pauline C, Feuk, Lars, Halpern, Aaron L, Walenz, Brian P, ...
Presented here is a genome sequence of an individual human. It was produced from ∼32 million random DNA fragments, sequenced by Sanger dideoxy technology and assembled into 4,528 scaffolds,...
An MCMC algorithm for haplotype assembly from whole-genome sequence data
Bansal, Vikas, Halpern, Aaron L., Axelrod, Nelson, Bafna, Vineet
In comparison to genotypes, knowledge about haplotypes (the combination of alleles present on a single chromosome) is much more useful for whole-genome association studies and for making inferences...