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Mark Adams

dblp:73/1116 · DBLP profile ↗
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5ranked-venue papers
4as first author
0since 2021 · last 2016
—ORCID · none

Domains — the database's venue-derived domains; a paper can count in several

Systems, architecture and hardware · 1 · 1 first-authorSoftware engineering, systems software and programming languages · 1Theory of computation · 1 · 1 first-authorApplied, interdisciplinary, general and emerging computing · 1 · 1 first-author

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
2 papers
Bioinformatics and computational biology · 86% Computational science and engineering · 14%
Computer architecture, parallel and distributed computing, and storage systems
1 paper
High-performance computing · 100%
Theoretical computer science
1 paper
Graph algorithms and graph theory · 50% Distributed computing theory · 50%

Topics — the 10 heaviest of 10, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
comparative genomics
0.012001
The sequence of the human genome (abstract only) · RECOMB 2001
Bioinformatics and computational biology › sequence analysis › sequence assembly
genome assembly
0.012001
The sequence of the human genome (abstract only) · RECOMB 2001
Bioinformatics and computational biology › genomics › computational genomics
SNP detection
0.012001
The sequence of the human genome (abstract only) · RECOMB 2001
Bioinformatics and computational biology › genomics › genome sequencing
whole genome shotgun sequencing
0.012001
The sequence of the human genome (abstract only) · RECOMB 2001
Computational science and engineering
finite element analysis
0.011999
Parallel Multigrid Solver for 3D Unstructured Finite Element Problems · SC 1999
High-performance computing
scientific computing systems
0.011999
Parallel Multigrid Solver for 3D Unstructured Finite Element Problems · SC 1999
Bioinformatics and computational biology
genome annotation
0.012001
The sequence of the human genome (abstract only) · RECOMB 2001
Bioinformatics and computational biology › genome annotation
protein coding region prediction
0.012001
The sequence of the human genome (abstract only) · RECOMB 2001
Graph algorithms and graph theory
graph algorithms
0.011999
Parallel Multigrid Solver for 3D Unstructured Finite Element Problems · SC 1999
Distributed computing theory › distributed graph algorithms
maximal independent set
0.011999
Parallel Multigrid Solver for 3D Unstructured Finite Element Problems · SC 1999

Methods — techniques the papers use, named apart from their topics

parallel coarsening · 0.1geometric heuristics · 0.1maximal independent set · 0.0whole genome shotgun sequencing · 0.0paired-end sequencing · 0.0BAC-based hybrid assembly · 0.0maximal independent sets · 0.0
YearPublicationVenuePosition
2016 Formal Methods in Collaborative Projects
abstract
In this paper we address particular aspects of integration of formal methods in large-scale industrial projects, namely collaborative aspects. We review recent works addressing such aspects, identify some current trends and discuss directions for further research.
Anna Zamansky, Guillermo Rodríguez-Navas, Mark Adams, Maria Spichkova
ENASE3
2016 HOL Zero's Solutions for Pollack-Inconsistency
Mark Adams
ITP1
2016 Use of the Recursive Least Squares Filter for Self Interference Channel Estimation
abstract
This paper presents the use of recursive least squares for online estimation of the self interference channel for an In Band Full Duplex communications link without the use of half duplex pilot signals. By using a long effective filter length it is possible to overcome the extra interference of the receieved signal, and it proves to be an effective way to estimate the channel in all scenarios, but it provides the greatest efficiency gain over current methods with a short channel coherence time. Recursive least squares estimation provides a way to take advantage of the constant knowledge of the transmitted signal to track the channel while consuming relatively few computational resources. Introducing online RLS estimation for In-Band Full Duplex communication provides a way to take advantage of the self interference cancellation gains from digital cancellation without introducing additional protocol overhead to the transmissions.
Mark Adams, Vijay K. Bhargava
VTC Fall1
2001 The sequence of the human genome (abstract only)
abstract
A consensus sequence of the euchromatic portion of human genome has been generated by the whole genome shot-gun sequencing method that was developed while sequencing the genomes of Haemophilus influenzae and Drosophila melanogaster. The 2.9 billion bp sequence, was generated over nine months from 27,271,853 high quality sequence reads (≁5X coverage of the genome) from both ends of plasmid clones made from the DNA of five individuals: three females and two males of African-American, Asian-Chinese, Hispanic and Caucasian ethnicity. The coverage of the genome in cloned DNA represented by paired end-sequences exceeds 37X. Two assembly methods, a whole genome assembly and a regional hybrid assembly were utilized, combining BAC data from GenBank with Celera data. Over 90 assemblies of 500,000 bp or greater and 2510 million bp or larger. Analysis of the genome sequence reveals - 26,178 protein-encoding genes for which there is strong corroborating evidence and an additional 12,000 computationally derived genes with mouse homologues or other weak supporting evidence. Comparative genomic analysis indicates vertebrate expansions of genes associated with neuronal function, tissue-specific developmental regulation, and in the hemostasis and immune systems. DNA sequence comparisons among the five individuals provided locations of 2.6 million single nucleotide polymorphisms (SNPs). The haploid genomes of a randomly drawn pair of humans differ at a rate of one per 1,250 bp on average but there is marked heterogeneity in the level of polymorphism across the genome. Only 0.75% of the SNPs led to possibly dysfunctional proteins.
Mark Adams
RECOMB1
1999 Parallel Multigrid Solver for 3D Unstructured Finite Element Problems
abstract
Multigrid is a popular solution method for the system of linear algebraic equations that arise from PDEs discretized with the finite element method.The application of multigrid to unstructured grid problems, however, is not well developed.We discuss a method, that uses many of the same techniques as the finite element method itself, to apply standard multigrid algorithms to unstructured finite element problems.We use maximal independent sets (MISs) as a mechanism to automatically coarsen unstructured grids; the inherent flexibility in the selection of an MIS allows for the use of heuristics to improve their effectiveness for a multigrid solver.We present parallel algorithms, based on geometric heuristics, to optimize the quality of MISs and the meshes constructed from them, for use in multigrid solvers for 3D unstructured problems.We conduct scalability studies that demonstrate the effectiveness of our methods on a problem in large deformation elasticity and plasticity of up to 40 million degrees of freedom on 960 processor IBM PowerPC 4-way SMP cluster with about 60% parallel efficiency.
Mark Adams, James Demmel
SC1