Fdstools

- Fixed an issue that prevented manually marking additional alleles.
- Fixed an issue with restoring allele calls after the visualisation has been saved.
- Added ability to display background noise profiles operating on total read counts.
- Added ability to display multiple noise correction notes for a single sequence.
- Added ability to display and save notes based on the optional 'flags' column, such
as Novel allele calls from FindNewAlleles.
- Changed default minimum number of reads per strand for table filtering from 1 to 0.
- Changed the default bias threshold from 25% to 0% (disabled).

- Minor change to the calculation of percentage of forward reads to prevent
roundoff effects.

- Added an option to apply graph filtering before noise correction (on by
default).

- Fixed incorrect calculation of 'percentage of highest' if the 'sequence'
with the highest read count within a marker is the aggregated 'Other
sequences' data. In exceptional cases, this could have resulted in the
erroneous omission of an allele in the visualisation (graphs and/or
tables).

- Added 'Save page' link to HTML visualisations, which offers for download
a copy of the entire HTML visualisation including the user's changes.
- Added automatic allele calling to static visualisations.
- The net effect of the allele calling thresholds (table filtering options)
is now visualised in the graphs as a dashed vertical red line.

- Added tooltip support to HTML visualisations.
- The tooltip may include a 'new allele' note if the input sample was
analysed with FindNewAlleles.
- The allele tables in HTML visualisations will now grow much wider than
before if the screen (or window) is very narrow.
- Improved line breaking behaviour in the tables in HTML visualisations.
- Improved determination of column widths of the allele tables when
printing an HTML visualisation.
- When printing an HTML visualisation, the graph and the corresponding
table of a marker will be kept on the same page in all browsers now.
- Fixed glitch that caused 'Infinity%' or 'NaN%' to be written in some
cells in the allele tables in HTML visualisations.