Plasmid transfection may lead to random integration into
the genome at low frequency.
Not exact matches
Some of the earliest studies of cancer
genomes in AML noted that, within a single patient, there were subsets of mutations present
at lower allele
frequencies, suggesting that they're not present in all cells.
Reykjavik, ICELAND, 9 October 2011 — Scientists
at deCODE Genetics and academic collaborators from Iceland, Norway, Denmark, the Netherlands and the USA today report the discovery of
low frequency variants in the human
genome that associate with risk of gout, a common...
Reykjavik, ICELAND, 9 October 2011 — Scientists
at deCODE Genetics and academic collaborators from Iceland, Norway, Denmark, the Netherlands and the USA today report the discovery of
low frequency variants in the human
genome that associate with risk of gout, a common inflammatory arthritis, and serum uric acid levels.
Both of these cell line - associated XMRV
genomes were found to exhibit a
lower degree of intra-strain variation than previously reported for XMRV from 22Rv1 cells [20], with only 19 SNPs detected in the 22Rv1 - associated XMRV
genome at the 3 %
frequency cutoff by deep sequencing, and only 25 SNPs in the LNCaP - associated
genome (Fig. 7A; Table S1).