Anthony J. Cox

Orcid: 0000-0002-6534-749X

Affiliations:
  • Illumina Inc., San Diego, CA, USA
  • Wellcome Trust Sanger Institute, Cambridge, UK (2000-2002)


According to our database1, Anthony J. Cox authored at least 18 papers between 1999 and 2018.

Collaborative distances:

Timeline

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Bibliography

2018
Canvas SPW: calling de novo copy number variants in pedigrees.
Bioinform., 2018

2017
tHapMix: simulating tumour samples through haplotype mixtures.
Bioinform., 2017

AKT: ancestry and kinship toolkit.
Bioinform., 2017

2016
Lightweight LCP construction for very large collections of strings.
J. Discrete Algorithms, 2016

Manta: rapid detection of structural variants and indels for germline and cancer sequencing applications.
Bioinform., 2016

Rapid genotype refinement for whole-genome sequencing data using multi-variate normal distributions.
Bioinform., 2016

RLZAP: Relative Lempel-Ziv with Adaptive Pointers.
Proceedings of the String Processing and Information Retrieval, 2016

2015
NxTrim: optimized trimming of Illumina mate pair reads.
Bioinform., 2015

2014
BEETL-fastq: a searchable compressed archive for DNA reads.
Bioinform., 2014

Adaptive reference-free compression of sequence quality scores.
Bioinform., 2014

2013
Lightweight algorithms for constructing and inverting the BWT of string collections.
Theor. Comput. Sci., 2013

metaBEETL: high-throughput analysis of heterogeneous microbial populations from shotgun DNA sequences.
BMC Bioinform., 2013

2012
Large-scale compression of genomic sequence databases with the Burrows-Wheeler transform.
Bioinform., 2012

Comparing DNA Sequence Collections by Direct Comparison of Compressed Text Indexes.
Proceedings of the Algorithms in Bioinformatics - 12th International Workshop, 2012

Lightweight LCP Construction for Next-Generation Sequencing Datasets.
Proceedings of the Algorithms in Bioinformatics - 12th International Workshop, 2012

2011
Lightweight BWT Construction for Very Large String Collections.
Proceedings of the Combinatorial Pattern Matching - 22nd Annual Symposium, 2011

2010
CNAseg - a novel framework for identification of copy number changes in cancer from second-generation sequencing data.
Bioinform., 2010

1999
Row-Wise Backward Stable Elimination Methods for the Equality Constrained Least Squares Problem.
SIAM J. Matrix Anal. Appl., 1999


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