Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Michael Hultner"'
Publikováno v:
IEEE Pulse. 10:20-23
Genomic research is the driver of efforts to create personalized medicine and discover cures for cancer, rare diseases, and other serious health conditions. Thanks to the widespread availability of inexpensive genome sequencing technology, the field
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1afcf2343f3a428d4c21ea4d1aae404
https://doi.org/10.1109/mpuls.2019.2899747
https://doi.org/10.1109/mpuls.2019.2899747
Publikováno v:
Cancer Research. 76:3632-3632
Precision oncology requires predictive models for therapy selection using variety of biomarkers and clinical features as input. Building and validating these models requires analysis of large numbers of diverse cases in order to relate markers and tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74517d695c96427c8f45e47912c241ff
https://doi.org/10.1158/1538-7445.am2016-3632
https://doi.org/10.1158/1538-7445.am2016-3632
Similarity landscapes: A way to detect many structural and sequence motifs in both introns and exons
Publikováno v:
Journal of Molecular Evolution. 38:188-203
When investigators undertake searches of DNA databases, they normally discard large numbers of alignments that demonstrate very weak resemblances to each other, retaining only those that show statistically significant levels of resemblance. We show h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::76aad38b0d09b08ca2f184e896598114
https://doi.org/10.1007/bf00166165
https://doi.org/10.1007/bf00166165
Publikováno v:
CogSIMA
We propose a Deception Robust Control (DRC) for orchestrating the cyber sensors and cyber effectors present in typical enterprise information network systems operating in the ever changing situations that arise in servicing their missions. The theory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8cc29bfc4b4fe9abb5524f7034d2ba08
https://doi.org/10.1109/cogsima.2011.5753754
https://doi.org/10.1109/cogsima.2011.5753754
Publikováno v:
Cancer Research. 75:4743-4743
Our understanding of the genetic basis for cancer is advancing at a rapid rate due to the application of next generation sequencing (NGS) technologies. It is becoming common to sequence tumors and patients in an attempt to find actionable mutations t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c64d14c505432879a72dc63d2ba0f9e6
https://doi.org/10.1158/1538-7445.am2015-4743
https://doi.org/10.1158/1538-7445.am2015-4743