TY - GEN
T1 - Use of average mutual information for studying changes in HIV populations
AU - Sayood, Khalid
AU - Hoffman, Federico
AU - Wood, Charles
PY - 2009
Y1 - 2009
N2 - Average mutual information (AMI) has been used in a number of applications in bioinformatics. In this paper we present its use to study genetic changes in populations; in particular populations of HIV viruses. Disease progression of HIV-1 infection in infants can be rapid resulting in death within the the first year, or slow, allowing the infant to survive beyond the first year. We study the development of rapid and slow progressing HIV population using AMI charts based on average mutual information among amino acids in the env gene from a population of 1142 clones derived from seven infants with slow progressing HIV-1 infection and four infants with rapidly progressing HIV-1 infection. The AMI charts indicate the relative homogeneity of the rapid progressor populations and the much greater heterogeneity of the slow progressor population, especially in later samples. The charts also show the distinct regions of covariation between residues without the need for aligning the sequences. By examining the changes in AMI between populations we can distinguish between clones obtained from rapid progressor and slow progressor. A measure of this change can be used to enhance prediction of disease progression.
AB - Average mutual information (AMI) has been used in a number of applications in bioinformatics. In this paper we present its use to study genetic changes in populations; in particular populations of HIV viruses. Disease progression of HIV-1 infection in infants can be rapid resulting in death within the the first year, or slow, allowing the infant to survive beyond the first year. We study the development of rapid and slow progressing HIV population using AMI charts based on average mutual information among amino acids in the env gene from a population of 1142 clones derived from seven infants with slow progressing HIV-1 infection and four infants with rapidly progressing HIV-1 infection. The AMI charts indicate the relative homogeneity of the rapid progressor populations and the much greater heterogeneity of the slow progressor population, especially in later samples. The charts also show the distinct regions of covariation between residues without the need for aligning the sequences. By examining the changes in AMI between populations we can distinguish between clones obtained from rapid progressor and slow progressor. A measure of this change can be used to enhance prediction of disease progression.
UR - http://www.scopus.com/inward/record.url?scp=77951003206&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=77951003206&partnerID=8YFLogxK
U2 - 10.1109/IEMBS.2009.5332579
DO - 10.1109/IEMBS.2009.5332579
M3 - Conference contribution
C2 - 19963600
AN - SCOPUS:77951003206
SN - 9781424432967
T3 - Proceedings of the 31st Annual International Conference of the IEEE Engineering in Medicine and Biology Society: Engineering the Future of Biomedicine, EMBC 2009
SP - 3861
EP - 3864
BT - Proceedings of the 31st Annual International Conference of the IEEE Engineering in Medicine and Biology Society
PB - IEEE Computer Society
T2 - 31st Annual International Conference of the IEEE Engineering in Medicine and Biology Society: Engineering the Future of Biomedicine, EMBC 2009
Y2 - 2 September 2009 through 6 September 2009
ER -