Animals that share a recent common ancestor would have
more nucleotide sequences in common than would more distantly related animals.
Not exact matches
It is a term of art in patent law that renders the claim «open - ended» so that it covers both the listed
nucleotide sequence and,
more importantly, the listed
sequence in combination with additional
sequences.
We present a draft
sequence of the Neandertal genome composed of
more than 4 billion
nucleotides from three individuals.
Release 155, produced in August 2006, contained over 65 billion
nucleotide bases in
more than 61 million
sequences.
But origin DNA
sequences contain
more A and T
nucleotides than usual.
Zhang compared the DNA
nucleotide sequence of the human version of ASPM to that of two of our great ape cousins, the chimpanzee and the orangutan, as well to
more distantly related animals such as rhesus monkeys, seals, dogs, and hamsters.
Where the Neanderthal had gene variants for a larger skull, for instance, Church would use MAGE to modify the
nucleotide sequences that constituted those genes in one or
more of the chunks of human DNA.
To make the match
more specific, Cas9 requires an additional
sequence flanking the targeted 20
nucleotides: N - G - G, in which «N» can be any
nucleotide.
Development of a high - throughput
sequence - independent amplification strategy for dsRNA viruses will increase our ability to
sequence more diverse rotavirus strains, including clinical isolates from both humans and animals, regardless of their
nucleotide sequence diversity.
Whole - genome
sequencing (WGS) marks the final step in increasing genetic marker density by assaying all single -
nucleotide variants (SNVs), and thus has the potential to further improve relationship detection by enabling
more accurate detection of IBD segments and
more precise resolution of IBD segment boundaries.
Microarray studies and,
more recently, exome
sequencing have demonstrated the importance of de novo copy number variations (CNVs) and single -
nucleotide variations (SNVs) in ID, but the majority of cases remains undiagnosed.
With
more than 15 million entries in dbSNP, single
nucleotide polymorphisms (SNPs) remain the most common form of DNA
sequence variation in humans.
In 1999 the nucleic acid
sequence archives contained a total of 3.5 billion
nucleotides, slightly
more than the length of a single human genome; a decade later they contained
more than 283 billion
nucleotides, the length of about 95 human genomes.