Major updates: New command-line argument "--synonymSequencePath" in order to supply additional reference variants (other than the wild-type) for which synonymous substitution variant fitness and error estimates are required "all_variants" R object now excludes synonymous variants for coding sequences (i.e. only WT and missense mutations); these are instead included in the "synonymous" R object (previously "silent" R object) "fitness_doubles.txt" output file now contains all doubles (not just those where both constituent singles were quantified) Minor updates: Synonymous variant fitness and error estimates are now provided when "--mixedSubstitutions" option set to TRUE Synonymous variants saved to "fitness_synonymous.txt"( instead of "fit...
While synonymous mutations were long thought to be without phenotypic consequences, there is growing...
<div><p>A diversity of tools is available for identification of variants from genome sequence data. ...
Whole Exome Sequencing (WES) is used for querying DNA variants using the protein coding parts of gen...
Major updates: Support for indel variants (see "indels" command-line arguments) Removed "vsearch...
Major updates: Fixed bug when translating sequences using Biostrings::translate which by default as...
Major updates: Performance improvements and approximately 10-fold reduced volume of data input and ...
What's Changed Added functions, vignettes, and unit tests to perform sample size calculations relat...
VariantsOfInterest - fixed a bug which removes NAs from mean frequency calculation ...
Meaningful analysis of next-generation sequencing (NGS) data, extensively produced by genomics studi...
Deep mutational scanning (DMS) enables multiplexed measurement of the effects of thousands of varian...
Minor updates: Infer growth rates from read counts if columns including "cell_density" (optical den...
This release includes the following changes: Fix frequency of bases when indels are also present. N...
New features: Added count mode. This allows the user to specify a file containing counts for each e...
Minor updates: Fixed issue #6 related to negative scaling factors in replicate normalisation parame...
Changes Implement an approach to calculate the probability of an undetected somatic mutation Implem...
While synonymous mutations were long thought to be without phenotypic consequences, there is growing...
<div><p>A diversity of tools is available for identification of variants from genome sequence data. ...
Whole Exome Sequencing (WES) is used for querying DNA variants using the protein coding parts of gen...
Major updates: Support for indel variants (see "indels" command-line arguments) Removed "vsearch...
Major updates: Fixed bug when translating sequences using Biostrings::translate which by default as...
Major updates: Performance improvements and approximately 10-fold reduced volume of data input and ...
What's Changed Added functions, vignettes, and unit tests to perform sample size calculations relat...
VariantsOfInterest - fixed a bug which removes NAs from mean frequency calculation ...
Meaningful analysis of next-generation sequencing (NGS) data, extensively produced by genomics studi...
Deep mutational scanning (DMS) enables multiplexed measurement of the effects of thousands of varian...
Minor updates: Infer growth rates from read counts if columns including "cell_density" (optical den...
This release includes the following changes: Fix frequency of bases when indels are also present. N...
New features: Added count mode. This allows the user to specify a file containing counts for each e...
Minor updates: Fixed issue #6 related to negative scaling factors in replicate normalisation parame...
Changes Implement an approach to calculate the probability of an undetected somatic mutation Implem...
While synonymous mutations were long thought to be without phenotypic consequences, there is growing...
<div><p>A diversity of tools is available for identification of variants from genome sequence data. ...
Whole Exome Sequencing (WES) is used for querying DNA variants using the protein coding parts of gen...