Silence's specific siRNA molecules exhibit unique structural features which, irrespective of
their individual nucleotide sequence, bar third parties from commercialising this type of molecule.
Not exact matches
We present a draft
sequence of the Neandertal genome composed of more than 4 billion
nucleotides from three
individuals.
They reveal 341 fixed substitutions (35 nonsynonymous, 173 synonymous, and 133 noncoding) between the 2014 EBOV and all previously published EBOV
sequences, with an additional 55 single -
nucleotide polymorphisms (SNPs; 15 nonsynonymous, 25 synonymous, and 15 noncoding), fixed within
individual patients, within the West African outbreak.
In the 7 May 2010 issue of Science, an international team of researchers presents the draft
sequence of the Neandertal genome composed of over 3 billion
nucleotides from three
individuals.
Bustamante and Poznik obtained highly accurate
sequencing results over a length of about 10 megabases of Y chromosome DNA (or 10 million
nucleotides) for each of the 69
individuals.
However, based on data now available, we see that the
sequence of the 3 billion
nucleotides in any
individual genome is unique in comparison with the
sequence of another
individual's genome, while the degree of
sequence similarity between the 3 billion
nucleotides in any two genomes is remarkably high.
Then, in 2010, Pääbo and colleagues published a draft
sequence of the Neanderthal's nuclear genome — 4 billion
nucleotides — based on three
individuals.
Called the stairway plot, it models the frequency of single
nucleotide polymorphisms (SNPs) in whole genome
sequences of hundreds of
individuals.
To generate whole - genome and
individual gene
nucleotide phylogeny trees, all 95 fully
sequenced unique adenovirus genomes were first downloaded from GenBank.
The term «single -
nucleotide polymorphism» (SNP) refers to a single base change in DNA
sequence between two
individuals.
Scott D. Collins, Ph.D., University of Maine, Orono $ 850,000 (2 years) «High - speed Nanopore Gene
Sequencing» Skilled in silicon fabrication methods, this group will try to fabricate a nanopore with tiny electrodes and built - in circuits that will be used in experiments that attempt to measure differences in the electron tunneling of
individual nucleotides in DNA molecules.
A single DNA
sequence is formed from a chain of four
nucleotide bases and if some
individuals in a population do not carry the same
nucleotide at a specific position in the
sequence, the variation is classified as an SNP.
After
sequence read quality and damage filtering (Supplementary Fig. 4), we called per -
individual consensus
sequences for
nucleotide positions covered by a minimum of two independent reads.
The resulting consensus
sequences averaged 16,231 ± 455 bp, or 98.1 % of the complete mitochondrial genome, with the average number of reads per
nucleotide position (fold -
sequence coverage) ranging from 7.4 × to 117 × among the 9
individuals (Supplementary Data 1).
At the highest level of resolution, the user can inspect the
nucleotide sequence of
individual genes.