Malicious host detection and classification in cloud forensics with DNN and SFLO approaches

Author(s):  
G. Nandita ◽  
T. Munesh Chandra
Author(s):  
Yakov V. Bubnov ◽  
Nick N. Ivanov

The problem of malicious host detection in a computer network is reviewed. Activity of computer network hosts is tracking by a noisy detector. The paper suggests method for detection malicious hosts using activity timeseries classification. The approach is based on hidden Markov chain model that analyses timeseries and consecutive search of the most probable final state of the model. Efficiency of the approach is based on assumption that advanced persisted threats are localised in time, therefore malicious hosts in a computer network can be detected by virtue of activity comparison with reliable safe hosts.


Author(s):  
Ryo Nakamura ◽  
Yuji Sekiya ◽  
Daisuke Miyamoto ◽  
Kazuya Okada ◽  
Tomohiro Ishihara

Author(s):  
Genevieve A M Lumsden ◽  
Evgeny V Zakharov ◽  
Sarah Dolynskyj ◽  
J Scott Weese ◽  
L Robbin Lindsay ◽  
...  

Abstract Using next-generation sequencing DNA barcoding, we aimed to determine: 1) if the larval bloodmeal can be detected in Ixodes scapularis nymphs and 2) the post-moult temporal window for detection of the larval bloodmeal. Subsets of 30 nymphs fed on a domestic rabbit (Oryctolagus cuniculus Linnaeus, Lagomorphia: Leporidae) as larvae were reared and frozen at 11 time points post-moult, up to 150 d. Vertebrate DNA was amplified using novel universal (UP) and species-specific primers (SSP) and sequenced for comparison against cytochrome c oxidase subunit I barcodes to infer host identification. Detectable bloodmeals decreased as time since moult increased for both assays. For the SSP assay, detection of bloodmeals decreased from 96.7% (n = 29/30) in day 0 nymphs to 3.3% (n = 1/30) and 6.7% (n = 2/30) at 4- and 5-mo post-moult, respectively. A shorter temporal detection period was achieved with the UP assay, declining from 16.7% (n = 5/30) in day 0 nymphs to 0/30 in 3-d-old nymphs. Bloodmeal detection was nonexistent for the remaining cohorts, with the exception of 1/30 nymphs at 2-mo post-moult. Host detection was significantly more likely using the SSP assay compared to the UP assay in the first three time cohorts (day 0: χ 2 = 39.1, P < 0.005; day 2: χ 2 = 19.2, P < 0.005; day 3: χ 2 = 23.3, P < 0.005). Regardless of the primer set used, the next-generation sequencing DNA barcoding assay was able to detect host DNA from a larval bloodmeal in the nymphal life stage; however, a short window with a high proportion of detection post-moult was achieved.


2002 ◽  
Vol 8 (S02) ◽  
pp. 962-963 ◽  
Author(s):  
W. J. Keyes ◽  
D. G. Lynn ◽  
W. K. Erbil ◽  
J. V. Taylor ◽  
R. P. Apkarian
Keyword(s):  

2016 ◽  
Vol 18 ◽  
pp. 77-78 ◽  
Author(s):  
Kim-Kwang Raymond Choo ◽  
Martin Herman ◽  
Michaela Iorga ◽  
Ben Martini

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