An efficient procedure for genotyping single nucleotide polymorphisms.
By S. Ye, S. Dhillon, X. Ke, A. Collins, Ian N. M. Day. Nucleic Acids Research, 2001
1,064 citations recorded by the source corpus.
Subfields: Molecular Biology
View Paper: https://www.semanticscholar.org/paper/bb0a09c97a7bd33f8a477760ca7d01c4d40c6507
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In Molecular Biology
Citations in the corpus
- Accessing genetic variation: genotyping single nucleotide polymorphisms (2001, methodology): “Alternatively, size separation in a high-throughput mode might be accomplished by using 96-channel capillary sequencing instruments, microplate array diagonal electrophoresi”
- Identification of Crassostrea ariakensis and Related Oysters by Multiplex Species-Specific PCR (2008, methodology): “To enhance specific amplification, a mismatch was introduced at the 3# end of some primer (Little 1997, Ye et al. 2001).”
- Large-scale association studies of variants in genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) confirm that the KCNJ11 E23K variant is associated with type 2 diabetes. (2003, background): “tion refractory mutation system) (23), and no discrepancies were found.”
- BatchPrimer3: A high throughput web application for PCR and sequencing primer design (2008, methodology): “To enhance the specificity in the AS-PCR reaction, an additional mismatch may be deliberately introduced at the third or other position from the 3' end of each of the AS primers [16,24-26].”