Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Sean A. Irvine"'
Autor:
Justin M. Zook, Len Trigg, Chunlin Xiao, Justin Wagner, Sean A. Irvine, Haynes Heaton, Jennifer McDaniel, Hemang Parikh, Francisco M. De La Vega, Cory Y. McLean, Stephen T. Sherry, Nathan D. Olson, Rebecca Truty, Marc L. Salit
Publikováno v:
Nature biotechnology
Benchmark small variant calls are required for developing, optimizing and assessing the performance of sequencing and bioinformatics methods. Here, as part of the Genome in a Bottle (GIAB) Consortium, we apply a reproducible, cloud-based pipeline to
Publikováno v:
Information Security Journal: A Global Perspective. 27:57-75
Automatic recognition of correct solutions as a result of a ciphertext only attack of simple ciphers is not a trivial issue and still remains a taxing problem. A new compression based method for th...
Autor:
Sean A. Irvine, Andrew R. Booker
Publikováno v:
Booker, A R & Irvine, S 2016, ' The Euclid-Mullin graph ', Journal of Number Theory, vol. 165, pp. 30-57 . https://doi.org/10.1016/j.jnt.2016.01.013
We introduce the Euclid-Mullin graph, which encodes all instances of Euclid's proof of the infinitude of primes. We investigate structural properties of the graph both theoretically and numerically; in particular, we prove that it is not a tree.
Autor:
John P. Overington, Anne Hersey, Sean A. Irvine, Nicholas T. Goncharoff, James Siddle, Nathan Dedman, Joe Pettersson, Richard Koks, Jon Chambers, George Papadatos, Anna Gaulton, Mark Davies
Publikováno v:
Nucleic Acids Research
SureChEMBL is a publicly available large-scale resource containing compounds extracted from the full text, images and attachments of patent documents. The data are extracted from the patent literature according to an automated text and image-mining p
Autor:
Justin M. Zook, Jennifer McDaniel, Hemang Parikh, Haynes Heaton, Sean A. Irvine, Len Trigg, Rebecca Truty, Cory Y. McLean, Francisco M. De La Vega, Chunlin Xiao, Stephen Sherry, Marc Salit
Benchmark small variant calls from the Genome in a Bottle Consortium (GIAB) for the CEPH/HapMap genome NA12878 (HG001) have been used extensively for developing, optimizing, and demonstrating performance of sequencing and bioinformatics methods. Here
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6851a1157acb4b7fed4df71cdd90e08
https://doi.org/10.1101/281006
https://doi.org/10.1101/281006
Publikováno v:
Cryptology and Network Security ISBN: 9783319489643
CANS
CANS
Automatically recognising valid decryptions as a result of ciphertext only cryptanalysis of simple ciphers is not an easy issue and still considered as a taxing problem. In this paper, we present a new universal compression-based approach to the auto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af517c2d5cb3a9ba7056f512ffef56c3
https://doi.org/10.1007/978-3-319-48965-0_3
https://doi.org/10.1007/978-3-319-48965-0_3
Autor:
Brian S Hilbush, Justin M. Zook, Alan Jackson, John G. Cleary, Richard Littin, Sean A. Irvine, David Ware, S. Inglis, Len Trigg, Ross Braithwaite, Francisco M. De La Vega, Mehul Kamlesh Rathod, Kurt Gaastra
To evaluate and compare the performance of variant calling methods and their confidence scores, comparisons between a test call set and a ?gold standard? need to be carried out. Unfortunately, these comparisons are not straightforward with the curren
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b7020e90502268f9b7334f18dee6d57a
Publikováno v:
Cancer Research. 77:3576-3576
Tumor molecular profiling is rapidly becoming the standard clinical test for selecting targeted therapies in refractory cancer patients. DNA extracted from patient samples is enriched for cancer genes and sequenced to identify actionable somatic muta
Autor:
John G Cleary, S. Inglis, Francisco M. De La Vega, Alan Jackson, Brian S Hilbush, Sean A. Irvine, Sahar Nohzadeh-Malakshah, Richard Littin, David Ware, Ross Braithwaite, Len Trigg, Mehul Kamlesh Rathod, Kurt Gaastra
Publikováno v:
Journal of computational biology : a journal of computational molecular cell biology. 21(6)
The analysis of whole-genome or exome sequencing data from trios and pedigrees has been successfully applied to the identification of disease-causing mutations. However, most methods used to identify and genotype genetic variants from next-generation
Autor:
John G Cleary, David Ware, Mehul Kamlesh Rathod, Kurt Gaastra, Sahar Nohzadeh-Malakshah, Richard Littin, Francisco M. De La Vega, Minita Shah, S. Inglis, Len Trigg, Ross Braithwaite, Brian S Hilbush, Sean A. Irvine, Alan Jackson
The analysis of whole-genome or exome sequencing data from trios and pedigrees has being successfully applied to the identification of disease-causing mutations. However, most methods used to identify and genotype genetic variants from next-generatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01f3ff641361fa6a8f5cb4636e4068c2