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Car owners can make use of an on-board diagnostics scanner or an owner's manual to identify the meaning of a trouble code. Five-digit diagnostic trouble codes typically consist of one letter and four numbers (e.g. P0123).
How to use a microarray for genotyping. The video shows the process of extracting genotypes from a human spit sample using microarrays. Genotyping is a major use of DNA microarrays, but with some modifications they can also be used for other purposes such as measurement of gene expression and epigenetic markers.
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Next, these 24 message symbols are encoded using C2 (28,24,5) Reed–Solomon code which is a shortened RS code over . This is two-error-correcting, being of minimum distance 5. This is two-error-correcting, being of minimum distance 5.
The fundamental aspect of BRB-seq is the optimized sample barcode primers. Each barcoded nucleotide sequence includes an adaptor for primer annealing, a 14-nt long barcode that assigns a unique identifier to each individual RNA sample, and a random 14-nt long UMI that tags each mRNA molecule with a unique sequence to distinguish between original mRNA transcripts and duplicates that result from ...
Depiction of the restriction enzyme (endonuclease) HindIII cleaving a double-stranded DNA molecule at a valid restriction site (5'–A|AGCTT–3').. In biochemistry, a nuclease (also archaically known as nucleodepolymerase or polynucleotidase) is an enzyme capable of cleaving the phosphodiester bonds that link nucleotides together to form nucleic acids.
The M.CviPl methyltransferase was first described in 1998, where the gene was cloned from Chorella virus NYs-1. [10] After its discovery, the methyltransferase was used for nucleosome foot-printing as early as 2004, [11] but NOMe-seq was not officially described until 2012. [12]
The Bradford protein assay (also known as the Coomassie protein assay) was developed by Marion M. Bradford in 1976. [1] It is a quick and accurate [2] spectroscopic analytical procedure used to measure the concentration of protein in a solution.