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Anthony J Cox

Showing results (1-10 of 17) with videos related to

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Bioinformatics (Oxford, England)|May 11, 2013
Adaptive reference-free compression of sequence quality scoresLilian Janin, Giovanna Rosone, Anthony J Cox
Bioinformatics (Oxford, England)|June 22, 2014
BEETL-fastq: a searchable compressed archive for DNA readsLilian Janin, Ole Schulz-Trieglaff, Anthony J Cox
Bioinformatics (Oxford, England)|May 7, 2016
Rapid genotype refinement for whole-genome sequencing data using multi-variate normal distributionsRudy Arthur, Jared O'Connell, Ole Schulz-Trieglaff, et al.
Bioinformatics (Oxford, England)|September 17, 2016
AKT: ancestry and kinship toolkitRudy Arthur, Ole Schulz-Trieglaff, Anthony J Cox, et al.
Bioinformatics (Oxford, England)|May 5, 2012
Large-scale compression of genomic sequence databases with the Burrows-Wheeler transformAnthony J Cox, Markus J Bauer, Tobias Jakobi, et al.
Peerj|June 10, 2015
NxRepair: error correction in de novo sequence assembly using Nextera mate pairsRebecca R Murphy, Jared O'Connell, Anthony J Cox, et al.
Bioinformatics (Oxford, England)|October 14, 2017
Canvas SPW: calling de novo copy number variants in pedigreesSergii Ivakhno, Eric Roller, Camilla Colombo, et al.
BMC Bioinformatics|June 6, 2013
metaBEETL: high-throughput analysis of heterogeneous microbial populations from shotgun DNA sequencesChristina Ander, Ole B Schulz-Trieglaff, Jens Stoye, et al.
American Journal of Human Genetics|October 8, 2013
Haplotype estimation using sequencing readsOlivier Delaneau, Bryan Howie, Anthony J Cox, et al.
Bioinformatics (Oxford, England)|September 9, 2016
tHapMix: simulating tumour samples through haplotype mixturesSergii Ivakhno, Camilla Colombo, Stephen Tanner, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Bioinformatics (Oxford, England)|May 11, 2013
Adaptive reference-free compression of sequence quality scoresLilian Janin, Giovanna Rosone, Anthony J Cox
Bioinformatics (Oxford, England)|June 22, 2014
BEETL-fastq: a searchable compressed archive for DNA readsLilian Janin, Ole Schulz-Trieglaff, Anthony J Cox
Bioinformatics (Oxford, England)|May 7, 2016
Rapid genotype refinement for whole-genome sequencing data using multi-variate normal distributionsRudy Arthur, Jared O'Connell, Ole Schulz-Trieglaff, et al.
Bioinformatics (Oxford, England)|September 17, 2016
AKT: ancestry and kinship toolkitRudy Arthur, Ole Schulz-Trieglaff, Anthony J Cox, et al.
Bioinformatics (Oxford, England)|May 5, 2012
Large-scale compression of genomic sequence databases with the Burrows-Wheeler transformAnthony J Cox, Markus J Bauer, Tobias Jakobi, et al.
Peerj|June 10, 2015
NxRepair: error correction in de novo sequence assembly using Nextera mate pairsRebecca R Murphy, Jared O'Connell, Anthony J Cox, et al.
Bioinformatics (Oxford, England)|October 14, 2017
Canvas SPW: calling de novo copy number variants in pedigreesSergii Ivakhno, Eric Roller, Camilla Colombo, et al.
BMC Bioinformatics|June 6, 2013
metaBEETL: high-throughput analysis of heterogeneous microbial populations from shotgun DNA sequencesChristina Ander, Ole B Schulz-Trieglaff, Jens Stoye, et al.
American Journal of Human Genetics|October 8, 2013
Haplotype estimation using sequencing readsOlivier Delaneau, Bryan Howie, Anthony J Cox, et al.
Bioinformatics (Oxford, England)|September 9, 2016
tHapMix: simulating tumour samples through haplotype mixturesSergii Ivakhno, Camilla Colombo, Stephen Tanner, et al.
Pageof 2