Changes Added a custom step phasing of clonal mutations. All clonal mutations (ie: clonal/not clonal determined by VAF) on the same amino acid are merged into a single mutation. This is not a read-backed phasing implementation which would allow to also phase intrahost mutations. Removed vt for decomposing complex mutations as the dependency was causing difficult to diagnose troubles in conda environments and it has virtually no impact in the output Improved documentatio
Mutations identified using next generation sequencing as stratified by the European society of medic...
Changes Replace Picard mark duplicates by sambamba Remove unnecessary sort operation Limits memory ...
<p>(A) In total, 117 mutational events (<a href="http://www.plosgenetics.org/article/info:doi/10.137...
Changes Fixes #26 and #41 by annotating VCFs with homoplasmic problematic sites from DeMaio. These ...
Changes Integrate pangolin for lineage determination. Integrate VAFator to annotate mutations with ...
Changes Add support for input directly VCF (--vcf) files instead of FASTA or FASTQ files. These VCF...
Major changes: Add coverage analysis for FASTQ pipeline Add Pfam domain annotations in the outpu...
Bugfix release The variant normalization workflow cached in the assets folder was sometimes causi...
Observed transitions and transversions in mutational events in the Basel and Manson data sets and in...
<p>* Changes are defined as being within coding regions or at intron-exon boundaries and have a Phre...
none7noneDanielson S.R.; Carelli V.; Tan G.; Martinuzzi A.; Schapira A.H.V.; Savontaus M.L.; Cortopa...
Simulation model. A detailed description of the model used for generating the simulated data include...
Annotation of mutated peptide sequences (mps) with published or novel potential neo-epitope descript...
Bugfix Python dependencies are defined now in a more flexible way using the compatibility operator ...
Changes Add an initial sort step to avoid GATK strange behaviour with unsorted BAMs Record software...
Mutations identified using next generation sequencing as stratified by the European society of medic...
Changes Replace Picard mark duplicates by sambamba Remove unnecessary sort operation Limits memory ...
<p>(A) In total, 117 mutational events (<a href="http://www.plosgenetics.org/article/info:doi/10.137...
Changes Fixes #26 and #41 by annotating VCFs with homoplasmic problematic sites from DeMaio. These ...
Changes Integrate pangolin for lineage determination. Integrate VAFator to annotate mutations with ...
Changes Add support for input directly VCF (--vcf) files instead of FASTA or FASTQ files. These VCF...
Major changes: Add coverage analysis for FASTQ pipeline Add Pfam domain annotations in the outpu...
Bugfix release The variant normalization workflow cached in the assets folder was sometimes causi...
Observed transitions and transversions in mutational events in the Basel and Manson data sets and in...
<p>* Changes are defined as being within coding regions or at intron-exon boundaries and have a Phre...
none7noneDanielson S.R.; Carelli V.; Tan G.; Martinuzzi A.; Schapira A.H.V.; Savontaus M.L.; Cortopa...
Simulation model. A detailed description of the model used for generating the simulated data include...
Annotation of mutated peptide sequences (mps) with published or novel potential neo-epitope descript...
Bugfix Python dependencies are defined now in a more flexible way using the compatibility operator ...
Changes Add an initial sort step to avoid GATK strange behaviour with unsorted BAMs Record software...
Mutations identified using next generation sequencing as stratified by the European society of medic...
Changes Replace Picard mark duplicates by sambamba Remove unnecessary sort operation Limits memory ...
<p>(A) In total, 117 mutational events (<a href="http://www.plosgenetics.org/article/info:doi/10.137...