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* General changes in v1.0.0rc1:
  * Fixed bug that caused variant descriptions in allele names of
    non-STR markers to be prepended with plus signs similar to suffix variants
    in STR markers.  When attempting to convert these allele names back to raw
    sequences, FDSTools would crash with an 'Invalid allele name' error.
* Allelevis v2.0.1 (additionally):
  * In the tooltip in HTML visualisations, a line break may now only be
    inserted in allele names after an underscore character (_) or after a
    repeat block in STR allele names.  If the input file contains raw
    sequences, line breaks may now be introduced anywhere in the sequence.
* Samplevis v2.1.1:
  * Added tooltip support to HTML visualisations.  Moving the mouse pointer
    over one of the alleles in the graph now displays a tooltip giving
    per-strand read counts of that allele.  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.
  * In the tables in HTML visualisations, a line break may now only be inserted
    in allele names after an underscore character (_) or after a repeat block
    in STR allele names.  If the input file contains raw sequences, line breaks
    may now be introduced anywhere in the sequence.
  * 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 for sequences that had zero
    reads (before or after correction).  These cells will remain empty now.
* Pipeline v1.0.1 (additionally):
  * The Pipeline tool will now only write the command lines of the tools it
    runs if the -d/--debug option was specified.
* Library v1.0.1 (additionally):
  * Added proper examples for non-STR markers and aliases.
* Stuttermodel v1.1.1:
  * Minor change to internal variant representation.

* General changes in v0.0.6.dev1:
  * Tools that take a list of files as their argument (through the -i option or
    as positionals) now explicitly support glob patterns.  This means they will
    interpret '*' and '?' characters as wildcards for 'zero or more characters'
    and 'any one character', respectively.  On Unix-like systems this is
    generally done by the shell, but on Windows one had to specify every file
    name completely.
* BGEstimate v1.1.1:
  * Added option -p/--profiles which can be used to provide a previously
    created background noise profiles file.  BGEstimate will read starting
    values from this file instead of assuming zero noise.
* BGMerge v1.0.2:
  * Small code changes to facilitate explicit glob pattern matching support.
* Pipeline v1.0.1:
  * The Pipeline tool will no longer check the existence of the files specified
    for the -S/--in-samples option; instead, this is left to the downstream
    tools to find out, consistent with how this works with the other input file
    options.
* Allelevis v2.0.1:
  * Added tooltip support to HTML visualisations.  Moving the mouse pointer
    over a node or edge in the graph now displays a tooltip giving allele names
    and sample counts.
* Stuttermodelvis v2.0.1:
  * Changed the unit in the horizontal axis title from 'bp' to 'nt'.
* Library v1.0.1:
  * Updated some of the comments describing the sections.

* General changes in v0.0.5:
  * The TSSV tool now depends on version 0.4.0 of TSSV.
  * Added new Pipeline tool that runs one of three default analysis pipelines
    automatically given a configuration file with tool options and input/output
    file names. The three available pipeline options are 'reference-sample',
    analysing a single reference sample with TSSV and Stuttermark;
    'reference-database', analysing a collection of reference samples with
    BGEstimate and Stuttermodel; and 'case-sample', analysing a single case
    sample with TSSV, BGPredict, BGMerge, BGCorrect, and Samplestats.
  * Added new Library tool that creates an empty FDSTools library file. Users
    may optionally specify the intented use of the library (STR markers,
    non-STR-markers, or both). Only the sections that apply to the given types
    of markers will be included in the output. The [aliases] section is not
    included by default, but an option is available to add it.
  * Added new tool BGAnalyse which can be used to analyse the remaining amount
    of noise in reference samples after correction.  This tool is a more
    sensitive successor of the 'Blame' tool.
  * Added new visualisation BGAnalysevis for visualising data obtained from
    BGAnalyse. This visualisation allows for identifying unclean or otherwise
    suboptimal samples by comparing the lowest, highest, and/or total remaining
    noise after correction for each marker in each sample.
  * The Blame tool was removed in favour of BGAnalyse.
* Libconvert v1.1.0:
  * When converting to FDSTools format, Libconvert automatically creates an
    empty FDSTools library file with the same contents as what would be
    obtained from the new Library tool without arguments.
  * The -a/--aliases option was modified such that it has the same effect as
    the -a/--aliases option of the new Library tool. This means that without
    this option specified, the [aliases] section will not be present in the
    output anymore.
  * The ability of the Libconvert tool to produce an empty FDSTools library
    file if no input file was given has been removed from the documentation
    (but not from the tool itself).
* TSSV v1.0.2:
  * Added new option -n/--indel-score which can be used to increase the
    penalty given to insertions and deletions in the flanking sequences w.r.t.
    the penalty given to mismatches.
  * NOTE: Requires TSSV v0.4.0 or newer to be installed.
* Vis v1.0.2:
  * Changed default value of -n/--min-abs from 15 to 5.
  * Added -I/--input2 option, which allows for specifying a file with raw data
    points for Stuttermodelvis and Profilevis.
  * Added support for creating BGAnalysevis visualisations.
* Profilevis v2.0.0:
  * Replaced the simple Options overlay with responsive design options panels
    in HTML visualisations.
  * Alleles and sequences are now sorted by CE allele length when applicable.
  * Added option to plot BGHomRaw data on top of the profiles.
  * Added marker selection menu for easier filtering.
* BGRawvis v2.0.0:
  * Replaced the simple Options overlay with responsive design options panels
    in HTML visualisations.
  * Sequences are now sorted by CE allele length when applicable.
  * Changed default minimum number of reads from 15 to 5.
  * Added marker selection menu for easier filtering.
* Stuttermodelvis v2.0.0:
  * Replaced the simple Options overlay with responsive design options panels
    in HTML visualisations.
  * Fixed glitch that caused the graphs to be re-rendered twice when loading
    a file by drag-and-drop in HTML visualisations.
  * Fixed glitch that made it possible to replace the data that was embedded
    in an HTML visualisation through drag-and-drop.
  * Added repeat unit selection menu for easier filtering.
* Allelevis v2.0.0:
  * Replaced the simple Options overlay with responsive design options panels
    in HTML visualisations.
  * Reduced Vega graph spec complexity by using the new Rank transform to
    position the subgraphs.
  * Fixed glitch that caused unnecessary padding around the graph.
* Samplestats v1.1.0:
  * Changed default allele calling option thresholds:
    * Changed default value of -m/--min-pct-of-max from 5.0 to 2.0.
    * Changed default value of -p/--min-pct-of-sum from 3.0 to 1.5.
  * Mentioned allele calling in the tool descriptions.
* Samplevis v2.1.0:
  * Changed default minimum number of reads for graph filtering from 15 to 5.
  * Changed default table filtering options:
    * Percentage of highest allele per marker changed from 5% to 2%.
    * Percentage of the marker's total reads changed from 3% to 1.5%.
    * Minimum number of reads in both orientations changed from 0 to 1.

* Global changes in v0.0.4:
  * FDSTools will now print profiling information to stdout when the -d/--debug
    option was specified.
  * Fixed bug where specifying '-' as the output filename would be taken
    literally, while it should have been interpreted as 'write to standard out'
    (Affected tools: BGCorrect, Samplestats, Seqconvert, Stuttermark).
  * Added more detailed license information to FDSTools.
* BGEstimate v1.1.0:
  * Added a new option -g/--min-genotypes (default: 3). Only alleles that occur
    in at least this number of unique heterozygous genotypes will be
    considered. This is to avoid 'contamination' of the noise profile of one
    allele with the noise of another. If homozygous samples are available for
    an allele, this filter is not applied to that allele. Setting this option
    to 1 effectively disables it. This option has the same cascading effect as
    the -s/--min-samples option, that is, if one allele does not meet the
    threshold, the samples with this allele are excluded which may cause some
    of the other alleles of these samples to fall below the threshold as well.
* Stuttermodel v1.1.0:
  * Stuttermodel will now only output a fit for one strand if it could also
    obtain a fit for the other strand (for the same marker, unit, and stutter
    depth). This new behaviour can be disabled with a new -O/--orphans option.
  * Fixed bug that caused Stuttermodel to output only the raw data points for
    -1 and +1 stutter when normal output was supressed.
* BGCorrect v1.0.1:
  * Added new column 'weight' to the output. The value in this column expresses
    the number of times that the noise profile of that allele fitted in the
    sample.
* Samplestats v1.0.1:
  * Samplestats will now round to 4 or 5 significant digits if a value is
    above 1000 or 10000, respectively. Previously, this was only done for the
    combined 'Other sequences' values.
  * The 'Other sequences' lines will now also include values for
    total_recovery, forward_recovery, and reverse_recovery.
  * The total_recovery, forward_recovery, and reverse_recovery columns are no
    longer placed to the left of all the other columns generated by
    Samplestats.
  * The help text for Samplestats erroneously listed the X_recovery_pct instead
    of X_recovery.
  * Added support for the new 'weight' column produced by BGCorrect when the
    -a/--filter-action option is set to 'combine'.
* BGPredict v1.0.1:
  * Greatly reduced memory usage.
  * BGPredict will now output nonzero values below the threshold set by
    -n/--min-pct if the predicted noise ratio of the same stutter on the other
    strand is above the threshold. Previously, values below the threshold were
    clipped to zero, which may cause unnecessarily high strand bias in the
    predicted profile.
* BGMerge v1.0.1:
  * Reduced memory usage.
* TSSV v1.0.1:
  * Renamed the '--is_fastq' option to '--is-fastq'. It was the only option
    with an underscore instead of a hyphen in FDSTools.
  * Fixed crash that would occur if -F/--sequence-format was set to anything
    other than 'raw'.
* Libconvert v1.0.1:
  * Specifying '-' as the first positional argument to libconvert will now
    correctly interpret this as "read from stdin" instead of throwing a "file
    not found" error (or reading from a file named "-" if it exists).
* Seqconvert v1.0.1:
  * Internal naming of the first positional argument was changed from 'format'
    to 'sequence-format'. This was done for consistency with the
    -F/--sequence-format option in other tools, giving it the same name in
    Pipeline configuration files.
* Vis v1.0.1:
  * Added -j/--jitter option for Stuttermodelvis (default: 0.25).
  * Vis would not allow the -n/--min-abs and the -s/--min-per-strand options to
    be set to 0.
* Stuttermodelvis v1.0.0beta2:
  * HTML visualisations now support drawing raw data points on top of the fit
    functions. The points can be drawn with an adjustable jitter to reduce
    overlap.
  * Fixed a JavaScript crash that would occur in HTML visualisations if the
    Repeat unit or Marker name filter resulted in an invalid regular expression
    (e.g., when the entered value ends with a backslash).
  * Reduced Vega graph spec complexity by using the new Rank transform to
    position the subgraphs.
  * HTML visualisations made with the -O/--online option of the Vis tool will
    now contain https URLs instead of http.
* Samplevis v1.0.1:
  * Fixed a JavaScript crash that would occur in HTML visualisations if the
    Marker name filter resulted in an invalid regular expression (e.g., when
    the entered value ends with a backslash).
  * Reduced Vega graph spec complexity by using the new Rank transform to
    position the subgraphs.
  * Fixed a glitch where clicking the 'Truncate sequences to' label would
    select the marker spacing input.
  * The 'Notes' table cells with 'BGPredict' in them now get a light orange
    background to warn the user that their background profile was computed.
    If a sequence was explicitly 'not corrected', 'not in ref db', or
    'corrected as background only', the same colour is used.
  * The message bar at the bottom of Samplevis HTML visualisations will now
    grow no larger than 3 lines. A scroll bar will appear as needed.
  * HTML visualisations made with the -O/--online option of the Vis tool will
    now contain https URLs instead of http.
* BGRawVis v1.0.1:
  * Fixed a JavaScript crash that would occur in HTML visualisations if the
    Marker name filter resulted in an invalid regular expression (e.g., when
    the entered value ends with a backslash).
  * Reduced Vega graph spec complexity by using the new Rank transform to
    position the subgraphs.
  * HTML visualisations made with the -O/--online option of the Vis tool will
    now contain https URLs instead of http.
* Profilevis v1.0.1:
  * Fixed a JavaScript crash that would occur in HTML visualisations if the
    Marker name filter resulted in an invalid regular expression (e.g., when
    the entered value ends with a backslash).
  * Reduced Vega graph spec complexity by using the new Rank transform to
    position the subgraphs.
  * HTML visualisations made with the -O/--online option of the Vis tool will
    now contain https URLs instead of http.
* Allelevis v1.0.0beta2:
  * Fixed potential crash/corruption that could occur with very unfortunate
    combinations of sample names and marker names.
  * HTML visualisations made with the -O/--online option of the Vis tool will
    now contain https URLs instead of http.
  * Added two more colours to the legend, such that a maximum of 22 markers is
    now supported without re-using colours.
* Updated bundled D3 to v3.5.17.
* Updated bundled Vega to v2.6.0.

* Added Noise column to the allele tables.
* Added number of reads before correction to the allele tables.
* Added raw numbers of reads to the Correction and Recovery columns of
  the allele tables.
* Fixed issue with Samplevis HTML visualisations in Firefox and Internet
  Explorer that caused an uncessesary horizontal scroll bar in the
  options panel.

Changed:
* The PctRecovery as used for automatic allele selection in Samplevis
  HTML visualisations as well as Samplestats is now computed w.r.t. the
  number of reads after correction, instead of the number of reads
  before correction.

Added:
* Added X_recovery columns to the output of the Samplestats tool. The
  value is equal to X_add / X_corrected * 100.

Fixed:
* Fixed a glitch in Samplevis HTML visualisations, where it would fail
  to correctly maintain the user-(de)selected alleles when switching
  Split Markers on or off.

Removed:
* Removed -L/--check-length option from the TSSV tool, because it had no
  effect. Instead, the TSSV tool will always enforce the expected allele
  lengths specified in the library file. Behaviour has not changed.

Fixed:
* The -c/--stuttermark-column option of Allelefinder was not filtering
  out the non-ALLELE sequences as it was supposed to. (This issue was
  introduced in ce7f34fb, in which a bug was fixed that caused this
  option to filter all sequences, including the ones marked with ALLELE.
  So it turns out this option has been broken since 732e83ba.)

Improved:
* Allelefinder will no longer reject a marker based on the number of
  reads of 'Other sequences'.
* Adjusted sequence alignment parameters for mtDNA sequences to produce
  allele names that more closely follow historical mtDNA mutation
  nomenclature.

* Turned all '0.1dev' tool version numbers to '1.0.0'.
* Changed Stuttermark's version number from '1.5' to '1.5.0'.
* Added version numbers to the visualisations.
* Updated README.rst to include all tools, but removed the usage details
  of Stuttermark because it is highly impractical to include usage
  details for all tools in the README file. I'll leave that to the
  -h/--help option and the yet-to-write FDSTools User's Handbook.

FDSTools would sometimes produce suboptimal alignments. Most notably, it
it would produce multiple smaller insertions/deletions when the
difference between two sequences could be described by one larger
insertion/deletion in combination with a base substitution. The latter
description is often more biologically sound and also usually results in
a shorter allele name.

* Fixed a bug that sometimes caused FDSTools to choose an incorrect path
  through the alignment matrix, producing a suboptimal alignment.
* Tweaked the alignment parameters to produce more meaningful results.

This was missing from commit 29fcc171

Added:
* Added a new section expected_allele_length to the FDSTools library
  format. In this section, the minimum and (optionally) maximum allele
  length of each marker can be specified.
* Added -L/--check-length option to the TSSV tool. If specified, the
  tool will use the expected_allele_length values to filter the results.
* Samplevis can now truncate long allele names to a given number of
  characters (defaulting to 70).
* Added an option to Samplestats to keep negatives when filtering (abs
  filter).

Changed:
* Renamed the --aggregate-below-minimum option of the TSSV tool to
  --aggregate-filtered.

Improved:
* Added an option to read_sample_data_file such that other code can
  request or require that the X_corrected columns are used.
* Samplestats will now round to 4 or 5 significant digits if a value is
  above 1000 or 10000, respectively.
* BGHomRaw will no longer round the forward, reverse, and total columns.
* When generating mtDNA allele names, FDSTools will now try to avoid
  creating gaps in the alignment of the sequences against the reference.
* Grouped the filtering options of the TSSV tool in its help text.
* Cleaned up some leftover code for special sequence value handling
  (more specifically: code that expected ensure_sequence_format to
  return False for special sequence values, which it no longer does).
* Cleaned up some dead legacy code in reduce_read_counts.

New tool findnewalleles:
* Given a list of known sequences, this tool can go through sample data
  files to mark all sequences that are not on the list.

Fixed:
* BGHomRaw, BGEstimate, BGHomStats, Stuttermodel, and Blame did not
  ignore the 'Other sequences' and 'No data' values that may occur in
  the place of a sequence as they were supposed to.

Improved:
* BGHomRaw will now include the sample tag in the "Missing allele X of
  marker Y" error message.
  
Changed:
* The -F/--sequence-format argument from BGHomRaw now defaults to "raw".

Visualisations:
* Updated Vega to version 2.5.0.
* The new version of Vega allowed the sorting to be fixed in Samplevis,
  Profilevis, BGRawvis, and Stuttermodelvis.
* Samplevis:
  * The 'Other sequences' bars are now drawn with an outline only.
  * STR alleles are now sorted by allele length by default (this can be
    toggled with a checkbox in HTML visualisations, and with an option
    in the Vis tool).
  * Fixed the clipping of the start of long allele names when printing
    SVGs from Google Chrome.
  * Added a note (as '?' help tooltip) to the Common axis range option
    in the HTML visualisation, to inform the user of the fact that the
    Split markers option needs to be off for it to work.

Fixed:
* Fixed crash in Samplestats. It would crash if BGCorrect columns were
  present.
* Fixed glitch in Samplevis that allowed clicking the 'Other sequences'
  bars if the input data already contained the 'Other sequences' entry.

Improved:
* The TSSV tool will now drop any sequences that contain anything other
  than A, C, T, and G. If the -A option is given, these sequences will
  still be added to the marker aggregates. Many other tools will fail
  when confronted with such invalid sequences, especially when allele
  names need to be generated.
* In Samplevis, the sequences are now consistently sorted (except for
  some inconsistency caused by a bug in Vega). The sorting is based on
  read counts and is the same as used for the allele tables in Samplevis
  HTML visualisations.
* Added a comment line that mentions genome build GRCh38 and rCRS to the
  genome_position block in the libconvert output. This is mainly for
  documentation purposes; users are free to change this line if they use
  a different reference.
* Minor styling changes to Samplevis HTML visualisations.

* Samplevis now features a responsive design. The options have been
  moved from the overlay into a menu bar that changes place and shape
  depending on the width and height of the viewport.
* All option labels are now clickable. When clicked, the corresponding
  option receives focus.
* The 'Save image', 'Save table', and 'Clear manually added/removed'
  links are now always visible, but change appearance when unavailable.
* When a 'No data' line is found for one or more markers, a warning is
  displayed at the bottom of the screen.
* Fixed bug that caused user-selected and user-removed alleles to get
  lost when the corresponding marker is filtered out using the marker
  name filter.
* Fixed bug in the printing stylesheet that caused conforming browsers
  to break pages between the graph and the table of a marker, instead of
  avoiding to do so.
* In HTML visualisations with embedded data, the name of the sample data
  file is now shown in the place of the file selection element.

Other Samplevis fixes and improvements:
* Added option to show sequences that are filtered from the graphs as a
  single 'Other sequences' aggregate entry per marker (default: on).
* For alleles that end up at a negative read count after correction now
  have a strand balance line in the 'overlap' portion of their bar only.
* The strand bias mark is now correctly positioned when using the square
  root scale.

Improved:
* HTML visualisations with embedded data will now use a proper filename
  for the 'Save graph' and 'Save table' options.

Fixed:
* Fixed a javascript crash in Samplevis HTML Visualisations.
* Converted two unexpected tab characters to spaces in README.rst.

Improved:
* Samplestats will now sort the output by marker name.

Improved:
* Added -A/--aggregate-below-minimum option to the TSSV tool. This will
  add a line with 'Other sequences' to the output summing all sequences
  that were not reported because they had less reads than was specified
  with the -a/--minimum option.
* Clarified the help text for the -D/--dir option of the TSSV tool.

Fixed:
* Updated all tools to consistently handle cases where 'No data' or
  'Other sequences' occurs in place of a sequence.

Updated Stuttermark to v1.5. WARNING: This version of Stuttermark is
INCOMPATIBLE with output from previous versions of FDSTools and TSSV.

Introducing TSSV-Lite
* New tool tssv acts as a wrapper around TSSV-Lite (tssvl). Its primary
  purpose is to allow running TSSV-Lite without having to convert the
  FDSTools library to TSSV format, and to offer allelename output. Like
  all other tools in FDSTools, it also works with TSSV library files but
  its allele name generation capabilities are limited in that case.

Changed:
* TSSV-Lite and the new TSSV tool in FDSTools have two columns renamed
  w.r.t. the original TSSV program: 'name' has been changed to 'marker',
  and 'allele' has been changed to 'sequence'. All tools in FDSTools
  have been updated to use the new column names. This change affects
  Allelefinder, BGCorrect, BGEstimate, BGHomRaw, BGHomStats, BGPredict,
  Blame, Samplestats, Samplevis, Stuttermark, Stuttermodel, and
  Seqconvert. Note that this change will BREAK COMPATIBILITY of these
  tools with old data files.

Fixed:
* In Samplevis HTML visualisations, the "percentage recovery" table
  filtering option used the absolute number of recovered reads instead.
* Added PctRecovery to the tables in Samplevis HTML visualisations.
* BGPredict will now print a nice error message if the -n/--min-pct
  option is set to zero or a negative number, to avoid division by zero.
* Samplestats would crash if the input file contained the flags column.
* FDSTools would crash when trying to convert sequences to allele names
  using a TSSV library.

Improved:
* Libconvert will no longer include duplicate sequences in the STR
  defenition when converting to TSSV format and the reference sequence
  of one of the markers is the same as one of its aliases, or when
  aliases of one marker share one or more prefix or suffix sequences.
* Updated add_input_output_args() such that the output file is a
  positional argument (instead of -o) for tools that have a single input
  file and no support for batches.
* Updated add_sequence_format_args() such that the library file can be
  made a required argument.
* Refined the FDSTools package description, since FDSTools does more
  than just noise filteirng.
* FDSTools will now do a marginally better job at producing allele names
  for sequences that do not exactly match the provided STR pattern. When
  seeking the longest matching portion of the sequence, it will now also
  test the reversed sequence with a reversed pattern, which sometimes
  yields a longer match. It is still not optimal, though, but some
  refactoring has been done to move away from regular expressions.
* BGCorrect will now also fill in correction_flags for newly added
  sequences.
* Adjusted the help text of Samplestats to include the fact that the -c
  and -y options have an OR relation instead of an AND relation.
* BGCorrect, BGEstimate, BGHomRaw, BGHomStats, BGPredict, and
  Stuttermodel will now ignore special values that may appear in the
  place of a sequence (currently: 'Other sequences' and 'No data').

Removed:
* The -m/--marker-column and -a/--allele-column arguments of BGPredict
  had no effect and have been removed.

Visualisations:
* Updated bundled D3 to v3.5.12.
* In HTML visualisations, if the page is scrolled to the right edge when
  an option is changed that causes the graphs to become wider, the page
  now remains scrolled to the right.
* Samplevis HTML visualisations:
  * Added 'Clear manually added/removed' link to the table filtering.
  * Reduced flicker of the mouse cursor in Internet Explorer.
  * Added 'Common axis range' checkbox (only available when 'Split
    markers' is off).
  * Added 'Save table' link to save the table of selected alleles to a
    tab-separated file.
  * Added 'PctRecovery' column to the tables of selected alleles.
  * An alert box is now shown when a data file is loaded that contains
    markers that have 'No data'.
  * Added 'Percentage of total reads' to the graph filtering options.
  * Added a note to the table filtering options to explain that the
    minimum percentage correction and recovery have an OR relation.

Fixed:
* Fixed a crash in BGMerge.
* Fixed bug in BGCorrect that resulted in incorrect values in the
  *_add and *_corrected columns (yes, you, 8685a304).
* Fixed a glitch in BGCorrect that prevented it from ever writing
  corrected_bgestimate in the correction_flags column.

Improved:
* BGEstimate will now include the sample tag in the error messages for
  missing alleles and alleles with 0 reads.
* Strand bias lines in Samplevis are now clamped to the 0-100% range.
  BGCorrect may cause forward read percentages outside this range.

Visualisations:
* Updated Vega to version 2.4.2.
* Fixed drag-'n-drop behaviour for HTML visualisations in Internet
  Explorer and Firefox.
* Fixed the Save Image link when viewing HTML visualisations in
  Internet Explorer 10 and above.
* Added http-equiv="X-UA-Compatible" content="IE=edge" meta-tag to all
  visualisations to prevent Internet Explorer from entering quirks mode.
* Samplevis:
  * Fixed glitch that would sometimes cause a second horizontal scroll
    bar to appear.
  * Graphs now render much more quickly when 'Split markers' is on, and
    Chrome no longer crashes on large sample files with this option set.

Fixed:
* When converting STR allele names to sequences, FDSTools would reject
  any prefix variants with a false message stating that the variant does
  not match the reference sequence.
* The Samplestats tool would not allow the -b/--min-per-strand option to
  be set to zero.

Improved:
* Moved the flags generated by BGCorrect to a new column named
  correction_flags. Some of the values have been renamed for clarity,
  and this column now always contains a value.
  * The Samplestats tool will no longer add the not_corrected flag to
    each sequence, as it does not add the correction_flags column.
* The Samplestats tool now supports filtering sequences. For filtering,
  the same set of options is available as those used for marking
  alleles. The filtering options use upper case letters and have '-filt'
  appended to their long name. The new -a/--filter-action option defines
  what should be done with filtered sequencies. 'off', the default,
  disables filtering; 'combine' replaces filtered sequences with a new
  line containing aggregated data; 'delete' removes filtered sequences
  without leaving a trace.
  * The seqconvert tool is aware of the special 'Other sequences' value
    produced by Samplestats with -a/--filter-action set to 'combine'.
	Other tools will give an informative error message when the input
	contains this special value.
* The Samplestats tool now accepts non-integer and negative numbers for
  -n/--min-reads and -b/--min-per-strand because after correction read
  counts are not necessarily nonnegative integers anymore.
* The forward_correction and reverse_correction columns of Samplestats
  will now contain 0 if the sequence had exactly 0 reads both before and
  after correction (previously, this was -100).
* Renamed the _mp columns of Samplestats to _mp_sum ("per-marker
  percentage of the sum") and introduced _mp_max columns ("per-marker
  percentage of the maximum").
* Samplestats and Samplevis HTML visualisations will now mark a sequence
  as 'allele' if the minimum amount of correction OR the minimum number
  of recovered reads is reached (as opposed to AND). This allows alleles
  on stutter positions to be detected.

Changed:
* The -r/--min-recovery option of Samplestats has been renamed to
  -y/--min-recovery, analogous to the new -Y/--min-recovery-filt.

Visualisations:
* Updated Vega to version 2.4.1.
* Replaced the regular expression-based filters in all visualisations
  with a much simpler syntax. The new syntax uses space-separated search
  terms, defaulting to a 'contains'-type search method. If any search
  term is preceded by an equals sign, that term must be matched exactly.
  (The search terms themselves are actually still matched as regexes!)
* Added 'show negative alleles' option (default on) to Samplevis. When
  enabled, the graph filtering options work on abs(value) instead of the
  value itself.
* When sorting alleles in Samplevis, the allele name is now used as the
  final tiebreaker instead of the primary sorting column.
* HTML visualisations no longer re-render the entire graph when changing
  the width. The same holds true for the height setting of Allelevis.
* The tables in Samplevis HTML visualisations will now contain the
  information from BGCorrect's correction_flags column in the Notes
  column.

Fixed:
* In Samplevis HTML visualisations, the automatic allele selection was
  only checking the number of reverse reads for the 'minimum number of
  reads per orientation' setting.
* In Samplevis HTML visualisations, automatic allele selection would
  fail to select alleles that had exactly the given minimum number of
  reads.
* FDSTools would sometimes calculate incorrect and even negative repeat
  counts when producing TSSV-style sequences and allele names for
  sequences that did not exactly fit the STR structure given in the
  library.

Improved:
* The Samplestats tool now offers the same possibilities to mark alleles
  as Samplevis HTML visualisations do.
* In Samplevis HTML visualisations, user-removed alleles now have a line
  through their table row.
* Added a reference to https://docs.python.org/howto/regex in the sample
  tag parsing options section of the help text of many tools.
* FDSTools will now do a better job of finding the longest possible
  match of the STR repeat definition to produce TSSV-style sequences and
  allele names for seqences that do not exactly fit the STR structure
  given in the library.

Added:
* New visualisation type 'allele'. With Allelevis, you can generate a
  graph of the alleles of the reference samples (output from
  Allelefinder). (Known bug: it has a 'funny' amount of padding.)

Fixed:
* The Vis tool no longer crashes if you specify '-' as the input file
  without piping data in from another program. It will just produce a
  visualisation file with no embedded data instead.
* FDSTools would crash when generating an allele name for a sequence of
  an STR marker that contained the prefix and suffix of the marker but
  not the actual STR (yes, this happened).
* Stuttermodelvis would draw all 'All data' fits in the graphs of all
  repeat unit sequences, instead of just the 'All data' fit that was
  fitted to the data of a particular repeat sequence.

Improved:
* BGHomStats, BGHomRaw, and Samplestats now round their output to three
  significant digits.
* BGCorrect now rounds its output to 3 decimal positions.

Various enhancements to Samplevis HTML visualisations:
* Added a whole new set of options which are used to automatically
  select the true alleles in a sample.
* Added an option to split the graphs and the table up per marker.
* The selected alleles are no longer lost when the graphs are
  re-rendered due to changed options.
* Added some more columns to the table of selected alleles and made the
  table prettier.
* Added a dedicated stylesheet for printing, which transforms the web
  page into a nicely formatted report when printed.
* Option groups can now be hidden separately.
* Filtering options are now based on the read numbers after correction.
* The mouse cursor now changes to a 'pointer' style cursor (usually a
  hand with stretched index finger) when hovered over the clickable
  portion of the graph.

Visualisations:
* Updated Vega to version 2.4.0 and d3 to version 3.5.10.
* All visualisations now use signals to set the options. This allows
  them to be updated without re-parsing the entire graph spec in most
  cases, which is much faster.
* Using new cross-and-filter capabilities in bgrawvis, profilevis,
  samplevis, and stuttermodelvis. This greatly reduces Vega's memory
  usage and speeds up rendering.
* The name of the currently loaded data file is prepended to the page
  title in HTML visualisations.
* If a file is loaded into an HTML visualisation by drag-and-drop, the
  name of the loaded file is displayed on the file input element.
* A new -T/--title option for the Vis tool allows for specifying
  something that should be prepended to the page title of HTML
  visualisations. This is particularly useful when data is piped in,
  because no file name is available in that case.
* Asynchronous rendering of visualisations is now cancelled if a new
  asynchronous rendering task has already been scheduled (HTML
  visualisations only).

* New tool Samplestats computes various sequence-centric statistics for
  sample data files. Most statistics relate to correction amounts and
  are thus only included if the input file contains BGCorrect columns.
* The starting position can now be ommitted from the [genome_position]
  in FDSTools library files. A default value of 1 will be used in this
  case.
* The setup.py script can now also be run without explicitly specifying
  Python as the interpreter (it now has a shebang line).

Fixed:
* The 'to' base in variants called on mtDNA was incorrect. This bug could also cause FDSTools to crash.
* FDSTools would crash if you tried to generate an allele name for a primer dimer of an mtDNA marker. (Now, you get an insane but entirely accurate allele name instead.)
* Fixed bug that caused some perfectly valid mtDNA allele names to be rejected when attempting to convert them back to raw sequences.

Improved:
* You can now also specify the ending position of the markers in the FDSTools library. If you do, you may also additionally specify a second start position (and optionally also a second end position, and so on). FDSTools will interpret this as that the marker is the concatenation of each of these fragments. This was primarily introduced to support mtDNA fragments that contain (somewhere in the middle) the origin of mtDNA base numbering.
* More helpful error message when format violations are detected while parsing the library file.
* More helpful error message when the -e/--tag-expr regular expression could not be compiled.
* Added a paragraph about sequence alignment caching to the help text of Seqconvert.
* Added a 'flags' column to BGCorrect output, which gives information about the data that was used to do the correction.

Background noise profiles:
* Removed -C/--cross-tabular option from BGEstimate, BGPredict, and BGMerge and also removed the ability to read files in this format.
* BGEstimate, BGHomStats, and BGPredict now add a column 'tool' with their name to the output.

* The legend items now have more descriptive names and also include the
  strand balance line.
* Added 5% to the X axis scale, to reassure people that they are really
  seeing the entire bar.
* The X axis scale limits are now rounded to a 'nice' number and
  includes a label for its ending tick mark.
* Added filter for a minimum number of reads per orientation.
* Strand bias line now becomes red if less than a certain percentage
  (default 25) of reads is on one strand, and a star is placed at the
  end of the allele's bar.
* Alleles can be selected (and deselectd) by clicking them (HTML only).
  * Selected alleles appear with a green italic allele name.
  * Data for selected alleles is summarised in a table at the bottom of
    the page. This is WIP and currently only includes the read total.

Additions and improvements to the FDSTools library file format:
* New [genome_position] section in FDSTools-style library files allows
for specifying the chromosome and position of each marker.
* New [no_repeat] section in FDSTools-style library files allows for
including non-STR markers.
* Comma/semicolon/space-separated values in FDSTools-style library files
can now also be separated by tab characters and multiple consecutive
separators are no longer collapsed (with the exception of whitespace).
* If no prefix and/or suffix has been specified for an alias, the
prefix/suffix of the marker itself is used.
* Implemented support for non-STR markers (e.g. SNP clusters) and mtDNA
markers. Allele names of the latter follow mtDNA nomenclature.
* Improved the logic of generating STR allele names for sequences that
have a prefix or suffix sequence that was not included in the library
file.
* Updated and clarified various explanatory texts in generated FDSTools
library files.

Fixed:
* Fixed a bug that caused prefix/suffix variants in aliases to go
missing in allele names.

Improved file handling:
* Library files are now closed immediately after parsing them.
* Sample data input files are opened one at a time now.

Visualisations:
* Updated Vega to version 2.3.1.
* Worked around a bug in Google Chrome that caused the 'Save image' link
to stop working after having been used once.

Will complete this when updating to Vega 2.2.5 or newer, which
contains a new feature that I contributed specifically for this.

* Properly implemented the options on the StuttermodelVis HTML
  visualisation.
* Added filtering options for marker and repeat unit to
  StuttermodelVis.
* Added StuttermodelVis to the Vis tool.

General visualisation changes:
* Updated Vega to v2.2.4.
* Fixed glitch that caused mouseover events in HTML visualisations
  to stop working after the renderer was switched.
* The file name suggested by the Save Image link in HTML
  visualisations is now derived from the name of the loaded data
  file.

And thereby removed a dirty workaround for a bug I found.

* Added StuttermodelVis HTML file and JSON spec. The rendering
  works, but some of the options are not implemented yet. It is
  also not yet added to the Vis tool.
* Changed the order of stuttermodel's coefficients: 'a' used to be
  the most significant coefficient, now it is the least significant
  coefficient (the shift). The benefit of this is that when moving
  to higher-order polynomials, the extra coefficients do not change
  the meaning of the others. So 'a' is now always the shift, 'b' is
  the linear component, 'c' the quadratic, etc.
* Added some development notes (including todo list) that I had
  kept outside of the project until now.

* BGCorrect and Stuttermark will now exit with an error message if
  more than one input file for the same sample is specified and no
  separate output files are given. Previously these tools would
  just overwrite the output file repeatedly, discarding the output
  of all but the last data file of the sample.
* Removed to main() functions and related stubs from the tools
  because they are not actually runnable directly anyway.
* Added some more help text to some of the tools.
* Doubled the size of the marker name filter input element on the
  HTML visualisations.

Fixed:
* Fixed crash that would occur when an empty sequence (primer dimer) is converted from raw to TSSV-style (or allelename) format.
* Fixed bug in BGHomRaw that caused incorrect sample tags in the output.
* Fixed bug that caused allele names with negative CE numbers and names of primer dimers to be regarded as 'invalid allele names' even though FDSTools generated those names itself.
* Fixed crash when reading sample data while looking for an annotation column.
* Fixed bug in Allelefinder resulting in the complete absence of output that occurred when a column name with Stuttermark output was specified.

Changed:
* Restyled the Options box on HTML visualisations. It is now less transparent and oriented more vertically to reduce overlap with the visualisation. Options are now presented in groups.
* Updated Vega to version 2.2.1.

New:
* Added *_corrected columns to BGCorrect output for convenience. E.g., the total_corrected column contains the value of total-total_noise+tot...