2001
DOI: 10.1117/12.443044
|View full text |Cite
|
Sign up to set email alerts
|

<title>Feasibility of high-resolution oligonucleotide separation on a microchip</title>

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

0
12
0

Year Published

2006
2006
2024
2024

Publication Types

Select...
4
2

Relationship

0
6

Authors

Journals

citations
Cited by 14 publications
(12 citation statements)
references
References 0 publications
0
12
0
Order By: Relevance
“…Samples were barcoded with a unique combination of forward and reverse indexes allowing for simultaneous processing of multiple samples. PCR products were pooled, column-purified, and size selected through microfluidic DNA fractionation (Minalla & Dubrow, 2001). Consolidated libraries were quantified using quantitative real-time PCR using the Kapa iCycler qPCR kit (Bio-Rad) on a BioRad Myio before loading into the sequencer.…”
Section: Gut Microbiome Analysesmentioning
confidence: 99%
“…Samples were barcoded with a unique combination of forward and reverse indexes allowing for simultaneous processing of multiple samples. PCR products were pooled, column-purified, and size selected through microfluidic DNA fractionation (Minalla & Dubrow, 2001). Consolidated libraries were quantified using quantitative real-time PCR using the Kapa iCycler qPCR kit (Bio-Rad) on a BioRad Myio before loading into the sequencer.…”
Section: Gut Microbiome Analysesmentioning
confidence: 99%
“…Samples were barcoded with a unique combination of forward and reverse indexes allowing for simultaneous processing of multiple samples. PCR products were pooled, column-purified, and size-selected through microfluidic DNA fractionation 20 . Consolidated libraries were quantified by quantitative real-time PCR using the Kapa Bio-Rad iCycler qPCR kit on a BioRad MyiQ before loading into the sequencer.…”
Section: Methodsmentioning
confidence: 99%
“…Primers also contained Illumina tags and barcodes with unique combination of forward and reverse indexes to allow multiplexing. Pooled PCR products were column-purified and selected through microfluidic DNA fractionation based on size [37]. Real-time qPCR quantified consolidated libraries using the Kapa Bio-Rad iCycler qPCR kit on a BioRad MyiQ prior to sequencing.…”
Section: S Ribosomal Rna (Rrna) Gene Sequencing Dna Extraction Anmentioning
confidence: 99%