TY - CONF
T1 - Computational Methods for Analysis of Cryptic Recombination in the Performance of Genomic Recombination Detection Software
AU - Alhiyafi, Jamal
AU - Sebesan, Cavitha
AU - Lu, Shiyong
AU - Harriott, Melphine
AU - Jurczyszyn, Deborah
AU - Ritchie, Raquel P.
AU - Gonzales, Felicitas S.
AU - Ram, Jeffrey L.
N1 - The detection of recombination from DNA sequences is relevant to the understanding of evolutionary and molecular genetics. While programs such as GENECONV have been identified as detecting recombination more reliably than others, previous studies have not analyzed how many recombinations they fail to detect.
PY - 2007/5/21
Y1 - 2007/5/21
N2 - The detection of recombination from DNA sequences is relevant to the understanding of evolutionary and molecular genetics. While programs such as GENECONV have been identified as detecting recombination more reliably than others, previous studies have not analyzed how many recombinations they fail to detect. We develop a method for testing how often such programs fail to identify recombinations and how detectability is affected by pairwise differences among the parental sequences. Recombination of sequences having a range of average pairwise differences (APD) is simulated by a stochastic method, and then the history of recombinations is compared to the recombinations identified by GENECONV. With high APD, GENECONV fails to detect ~50% of recombinations; while at a more typical intraspecies APD of 1% to 2%, >70% of recombinations are undetected. Quantitative results suggest corrections for estimating recombination rates more accurately and methods to detect evidence of recombination more consistently.
AB - The detection of recombination from DNA sequences is relevant to the understanding of evolutionary and molecular genetics. While programs such as GENECONV have been identified as detecting recombination more reliably than others, previous studies have not analyzed how many recombinations they fail to detect. We develop a method for testing how often such programs fail to identify recombinations and how detectability is affected by pairwise differences among the parental sequences. Recombination of sequences having a range of average pairwise differences (APD) is simulated by a stochastic method, and then the history of recombinations is compared to the recombinations identified by GENECONV. With high APD, GENECONV fails to detect ~50% of recombinations; while at a more typical intraspecies APD of 1% to 2%, >70% of recombinations are undetected. Quantitative results suggest corrections for estimating recombination rates more accurately and methods to detect evidence of recombination more consistently.
UR - https://ieeexplore.ieee.org/document/4221141
U2 - 10.1109/AINAW.2007.124.
DO - 10.1109/AINAW.2007.124.
M3 - Presentation
T2 - 21st International Conference on Advanced Information Networking and Applications Workshops (AINAW'07)
Y2 - 21 May 2007
ER -