2022
DOI: 10.1016/j.fsigen.2022.102664
|View full text |Cite
|
Sign up to set email alerts
|

Analysis of mixed DNA profiles from the RapidHIT™ ID platform using probabilistic genotyping software STRmix™

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
5
0

Year Published

2022
2022
2024
2024

Publication Types

Select...
7

Relationship

1
6

Authors

Journals

citations
Cited by 9 publications
(6 citation statements)
references
References 29 publications
0
5
0
Order By: Relevance
“…Additionally, rapid DNA techniques are not or less suitable for resolving DNA mixtures [ 5 ]. This results in a trade-off between performance on one hand and speed and portability on the other [ 76 ].…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Additionally, rapid DNA techniques are not or less suitable for resolving DNA mixtures [ 5 ]. This results in a trade-off between performance on one hand and speed and portability on the other [ 76 ].…”
Section: Discussionmentioning
confidence: 99%
“…The sensitivity of the RapidHIT is lower than a standard laboratory workflow, which affects the results when touch samples are analyzed. Many of the analyzed touch DNA samples produced very low-level DNA profiles [ 76 ].…”
Section: Rapid Dna Systemsmentioning
confidence: 99%
“…These Rapid PCR programs are valuable to forensic investigations as they allow informative DNA profiles to be generated quickly, in the field at remote locations, and by personnel with little training. However, it is important to highlight that Rapid DNA has a specific range of applications, and currently has only had varying success with the suboptimal samples that are typically encountered in casework [95]. Thus, a major limitation of Rapid DNA cycling conditions is that they generally require high-quality samples (i.e., reference samples) to generate good-quality, informative DNA profiles [96].…”
Section: Short Tandem Repeat Profilingmentioning
confidence: 99%
“…The largest alteration to PCR cycling conditions in forensic science came with the introduction of Rapid DNA instruments to laboratory workflows. While the features and importance of Rapid DNA have already been discussed, it is important to emphasize that Rapid DNA was designed for high-quality samples (i.e., reference samples) and has only had varying success when used with sub-optimal samples [95]. This highlights an important limitation of Rapid DNA: it requires good-quality DNA samples to generate informative DNA profiles [96].…”
Section: Evolution Of Pcr Cycling Conditions In Other Disciplinesmentioning
confidence: 99%
“…Some attempts to extend the range of sample types to low quantities of DNA or mixtures have been published with various levels of success (see Table 4 ). Researcher and practitioners from Australia [ [40] , [41] , [42] ], Canada [ 43 ], China [ 44 ], Italy [ 45 ], Japan [ 46 , 47 ], and the United States [ [48] , [49] , [50] , [51] , [52] , [53] , [54] , [55] , [56] , [57] ] have contributed to an increased understanding of rapid DNA testing capabilities and limitations.…”
Section: Advancements In Current Practicesmentioning
confidence: 99%