Complete set of raw predictions obtained from all the variant effect predictors used in this study for every tubulin mutation. (CSV)</p
S5 Table represents results of ΔΔG prediction of 71 single mutations displayed in terms of chain, wi...
<p>The predicted mutation counts expressed in terms of the number of synonymous and non-synonymous s...
<p>Summary of Ensembl Variant Effect Predictor results for oocyan-unique SNPs in captured region.</p
DeepSequence predictions for every possible missense mutation for all tubulin isotypes considered in...
For each of the VEPs used in this study, cumulative distribution ranks were generated in a combined ...
Full description of all pathogenic mutations compiled in this study (including phenotypes and refere...
All ΔΔG values predicted using FoldX using both the structure of the monomeric subunit (ddG_fold) an...
Deep mutational scanning datasets used for 'Mutation Effect Prediction of Proteins using RoseTTAFold...
Names have been shortened by removing the “bioseq2” prefix for all of them. (A) Inter-replicate agre...
The effect of single nucleotide variants (SNVs) in coding and noncoding regions is of great interest...
Primary analysis files for bioRxiv manuscript with id 2019/859603 (https://www.biorxiv.org/content/1...
Prediction of mutation impact according to bioinformatics tools in patients and controls.</p
(A) ROC AUC values for each VEP across all tubulin-α and -β isotypes with at least one identified pa...
The proportion of pathogenic and putatively benign gnomAD mutations in each location type for tubuli...
Synonymous single nucleotide variants (sSNVs), a common type of genomic variant, does not alter the ...
S5 Table represents results of ΔΔG prediction of 71 single mutations displayed in terms of chain, wi...
<p>The predicted mutation counts expressed in terms of the number of synonymous and non-synonymous s...
<p>Summary of Ensembl Variant Effect Predictor results for oocyan-unique SNPs in captured region.</p
DeepSequence predictions for every possible missense mutation for all tubulin isotypes considered in...
For each of the VEPs used in this study, cumulative distribution ranks were generated in a combined ...
Full description of all pathogenic mutations compiled in this study (including phenotypes and refere...
All ΔΔG values predicted using FoldX using both the structure of the monomeric subunit (ddG_fold) an...
Deep mutational scanning datasets used for 'Mutation Effect Prediction of Proteins using RoseTTAFold...
Names have been shortened by removing the “bioseq2” prefix for all of them. (A) Inter-replicate agre...
The effect of single nucleotide variants (SNVs) in coding and noncoding regions is of great interest...
Primary analysis files for bioRxiv manuscript with id 2019/859603 (https://www.biorxiv.org/content/1...
Prediction of mutation impact according to bioinformatics tools in patients and controls.</p
(A) ROC AUC values for each VEP across all tubulin-α and -β isotypes with at least one identified pa...
The proportion of pathogenic and putatively benign gnomAD mutations in each location type for tubuli...
Synonymous single nucleotide variants (sSNVs), a common type of genomic variant, does not alter the ...
S5 Table represents results of ΔΔG prediction of 71 single mutations displayed in terms of chain, wi...
<p>The predicted mutation counts expressed in terms of the number of synonymous and non-synonymous s...
<p>Summary of Ensembl Variant Effect Predictor results for oocyan-unique SNPs in captured region.</p
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