Hietpas et al. (2013) |
6 or 7 |
568 |
30 |
for full replicates |
Beneficial single substitutions in Hsp90 of yeast under altered environments |
Jiang et al. (2013) |
6 or 7 |
568 |
34 |
for full replicates |
Interaction of expression and single substitutions on DFE of yeast Hsp90 |
Puchta et al. (2016) |
5–7 |
≈60,000 |
545.7 |
|
Network of epistatic interactions in yeast small nucleolar RNA |
Roscoe et al. (2013) |
6 |
1,530 |
21 |
for full replicates |
Functional biophysics of single substitutions in ubiquitin of yeast |
Hietpas et al. (2011) |
3 or 7 |
568 |
26 |
for full replicates |
DFE of single substitutions for a short region of Hsp90 in yeast |
Bank et al. (2015) |
5 |
1,015 |
21.6 |
Credibility intervals (figure 6B) |
DFE of epistatic substitutions in Hsp90 of yeast |
Wu et al. (2013) |
3 |
>400 |
>0.002 |
NA |
Compensatory single substitutions for neuraminidase mutant of influenza |
Li et al. (2016) |
2 |
65,537 |
685.5 |
mean across 15 pairs of biological replicates |
Fitness landscape of a transfer RNA gene in yeast |
Jiang et al. (2015) |
2 |
475 |
20.5 |
for full replicates |
Biophysics of single substitutions in influenza neuraminidase with antiviral |
Roscoe and Bolon (2014) |
2 |
1,617 |
30 |
for full replicates |
Biophysics of single ubiquitin substitutions on E1 activity and yeast fitness |
Melnikov et al. (2014) |
2 |
4,993 |
33.2 |
for full replicates |
Biophysics of single substitutions in APH(3′)II in Escherichia coli with antibiotics |
Kim et al. (2013) |
2 |
29,708 |
90.2 |
NA |
Biophysics of single substitutions in yeast Deg1 protein degradation signal |
Melamed et al. (2013) |
2 |
110,745 |
186.5 |
NA |
Biophysics of single and multiple substitutions in Pab1 RRM of yeast |
Klesmith et al. (2015) |
2 |
9,219 |
5.8 |
Reproducibility plot |
Biophysics of levoglucosan consumption rate in E. coli
|