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Showing 1 to 6 of 6 entries
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Human Y-chromosome SNP characterization by multiplex amplified product-length polymorphism analysis.

Electrophoresis

Medina LS, Muzzio M, Schwab M, Costantino ML, Barreto G, Bailliet G.
PMID: 24846779
Electrophoresis. 2014 Sep;35(17):2524-7. doi: 10.1002/elps.201400020. Epub 2014 Jul 14.

We designed an allele-specific amplification protocol to optimize Y-chromosome SNP typing, which is an unavoidable step for defining the phylogenetic status of paternal lineages. It allows the simultaneous highly specific definition of up to six mutations in a single...

Applying instructional design theories to bioinformatics education in microarray analysis and primer design workshops.

Cell biology education

Shachak A, Ophir R, Rubin E.
PMID: 16220141
Cell Biol Educ. 2005;4(3):199-206. doi: 10.1187/cbe.04-11-0055.

The need to support bioinformatics training has been widely recognized by scientists, industry, and government institutions. However, the discussion of instructional methods for teaching bioinformatics is only beginning. Here we report on a systematic attempt to design two bioinformatics...

"THE STORM BEFORE THE CALM"--A PRIMER.

Psychiatric communications

RUMBLE C.
PMID: 14235141
Psychiatr Commun. 1964;7:35-40.

No abstract available.

INFANTILE paralysis, or acute poliomyelitis; a brief primer of the disease and its treatment.

Journal of the American Medical Association

[No authors listed]
PMID: 20994367
J Am Med Assoc. 1946 Aug 24;131:1411-9.

No abstract available.

Getting things backwards to prevent primer dimers.

The Journal of molecular diagnostics : JMD

Poritz MA, Ririe KM.
PMID: 24457120
J Mol Diagn. 2014 Mar;16(2):159-62. doi: 10.1016/j.jmoldx.2014.01.001. Epub 2014 Jan 20.

This Commentary highlights the article by Satterfield that describes a new class of primer technology-cooperative primers, which prevent primer-dimer amplification.

Rapid and simple method of qPCR primer design.

Methods in molecular biology (Clifton, N.J.)

Thornton B, Basu C.
PMID: 25697660
Methods Mol Biol. 2015;1275:173-9. doi: 10.1007/978-1-4939-2365-6_13.

Quantitative real-time polymerase chain reaction (qPCR) is a powerful tool for analysis and quantification of gene expression. It is advantageous compared to traditional gel-based method of PCR, as gene expression can be visualized "real-time" using a computer. In qPCR,...

Showing 1 to 6 of 6 entries