2016
DOI: 10.1016/j.bios.2015.11.079
|View full text |Cite
|
Sign up to set email alerts
|

Total integrated slidable and valveless solid phase extraction-polymerase chain reaction-capillary electrophoresis microdevice for mini Y chromosome short tandem repeat genotyping

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1

Citation Types

0
9
0

Year Published

2016
2016
2024
2024

Publication Types

Select...
9
1

Relationship

0
10

Authors

Journals

citations
Cited by 33 publications
(9 citation statements)
references
References 35 publications
0
9
0
Order By: Relevance
“…However, it is a tedious and time-consuming process and involves a bulky gel bed setup; thus, it is not commonly used in clinical NA testing. 128 Since the 1990s, integration and parallelization of NA analyses on capillary electrophoresis-based microfluidic systems have been widely investigated, which enables efficient on-chip RNA/DNA testing; 148 however, these systems are generally complicated when both precise flow control and optical detection are needed, 149 hampering its usability in practical applications. In summary, optical detection methods are generally suitable for use on integrated diagnostic systems for NA-based virus testing, and can provide merits such as high testing throughput, satisfactory sensitivity and specificity, and good cost efficiency.…”
Section: Optical Detectionmentioning
confidence: 99%
“…However, it is a tedious and time-consuming process and involves a bulky gel bed setup; thus, it is not commonly used in clinical NA testing. 128 Since the 1990s, integration and parallelization of NA analyses on capillary electrophoresis-based microfluidic systems have been widely investigated, which enables efficient on-chip RNA/DNA testing; 148 however, these systems are generally complicated when both precise flow control and optical detection are needed, 149 hampering its usability in practical applications. In summary, optical detection methods are generally suitable for use on integrated diagnostic systems for NA-based virus testing, and can provide merits such as high testing throughput, satisfactory sensitivity and specificity, and good cost efficiency.…”
Section: Optical Detectionmentioning
confidence: 99%
“…Some examples include commercial microfluidic arrays (e.g. Fluidigm®) ( Von Thaden et al, 2017 ), microfluidic integration of sample preparation steps and/or amplification and detection steps, either based on allele-specific hybridization strategies for SNP genotyping ( Zec et al, 2018 ), or combined with microscale capillary electrophoresis (µCE) for SSR markers (Y. T. Kim et al, 2016 ). Other strategies include integration of microfluidic DNA amplification with microarrays ( Choi et al, 2012 ), primer extension on microbeads ( Chang et al, 2017 ) or implementation of HRM analysis ( Velez et al, 2017 ) at microscale.…”
Section: Introductionmentioning
confidence: 99%
“…By taking full advantage of microfluidics, many researchers have made intensive efforts to conduct entire procedures of nucleic acid extraction and amplification, such as PCR and loop-mediated isothermal amplification (LAMP), on a single microfluidic device. For example, Kim et al used silicon materials and a slidable chip with 70 mm-diameter silica beads to extract genomic DNA from whole human blood [19]. A microfluidic device for integrated DNA extraction and loop-mediated isothermal amplification using glass powder has been developed to detect the epidermal growth factor receptor (EGFR) L858R point mutation in NCI-HI1975 cells [20].…”
Section: Introductionmentioning
confidence: 99%