From: On an enhancement of RNA probing data using information theory
\(n=100\) | \(n=200\) | \(n=300\) | |
---|---|---|---|
\(d_{\text {sn}}(s,\Omega )/n\) | \(0.214 \pm 0.088\) | \(0.219\pm 0.068\) | \(0.217 \pm 0.063\) |
\(d_{\text {sn}}(s,\Omega _{\text {probe}})/n\) | \(0.035 \pm 0.021\) | \(0.034\pm 0.015\) | \(0.034\pm 0.012\) |
\(d_{\text {sn}}(s,\Omega ^{0.05})/n\) | \(0.031 \pm 0.008\) | \(0.038\pm 0.012\) | \(0.037\pm 0.018\) |
\(d_{\text {sn}}(s,\Omega ^{0.1})/n\) | \(0.074 \pm 0.014\) | \(0.080\pm 0.015\) | \(0.087 \pm 0.010\) |
\(d_{\text {sn}}(s,\Omega ^{0.15})/n\) | \(0.098 \pm 0.021\) | \(0.116 \pm 0.018\) | \(0.123 \pm 0.011\) |
\(d_{\text {sn}}(s,\Omega ^{0.20})/n\) | \(0.127 \pm 0.034\) | \(0.144 \pm 0.027\) | \(0.157 \pm 0.020\) |
\(d_{\text {sn}}(s,\Omega ^{0.25})/n\) | \(0.144 \pm 0.043\) | \(0.167 \pm 0.038\) | \(0.180 \pm 0.029\) |