- Miscellaneous
- File Compress allow ctrl-enter to force re-writing of a file 28.51
- tidier input memory 28.46
- menu reorganized. Save as and Retrieve replace
the former unclear option ASCII 28.42
- When a locus is "inactive" remove it from the locus-order list 28.28
- Search NDIS for relatives Custom feature under development (extra cost option)
27.41, 28.11, 28.24
- new PCR Parameter for genetic category (e.g. Y-chromosome) of locus
28.01
- better FileCompress 28.09
- Installation creates desktop folder with icons including new maintenance facility REPAIR. 27.47
- Spanish language option (work in progress) 27.36
- Profile data New command summarizes available data across several selected membranes,
shows details of any typing conflicts 27.34
- Input memory for fill-in responses: 27.24
- PgUp/PgDwn (or Ctrl-Dwn-arrow)
scroll to a previous input line.
- Up/Dwn arrows also scroll unless harnessed as screen movement.
- PgUp/PgDwn scroll through previous responses to multi-line input
(e.g. Kinship Type in scenario).
- Ctrl-Shift-Delete removes an item from the memory of responses.
- Ctrl-Up-Arrow pops up a menu of previous responses.
- select from the menu
- DEL deletes an item from the list of previous responses.
- Ctrl-z restores the original response.
- Race selection dialogue clearer 27.23
- On sign-off, better instructions for clearing phantom user names 27.21
- Main screen shows the location of DNAVIEW inconspicuously 27.19
- "Multiplex" definition (e.g. for Simulate) allows specification of a range
of loci useful for SNP's 27.19
- Read, Tablet Check send extra character to drive Graphtec under XP 27.18
- Create Katrina Cases Hurricane Katrina victim identification custom feature 27.31
- Honor previous role assignments. 27.47
- accept kin names; add to rather than replace former definitions 27.32
- creates cases from kinship spreadsheet 27.34
- Pro Busqueda special: Parse Probusq File
creates cases from kinship spreadsheet 27.16
bugfix don't assign a victim role to a reference
- allow deleting just the roster of a membrane/worklist 27.11
- Quit DNAVIEW new name for Exit from DNAVIEW easier to type
(because it is the only command beginning with Q) and more expected to a Windows user. 27.11
- When editing things like Kinship scenario or Options
DNA-VIEW report title, Ctrl-Ins/Del will insert or remove a line. 27.09
- Exit from DNAVIEW better display/explanation of
clearing spurious sign-ons 27.06
- text input recognizes arrows for navigation,
Ctrl-z to restore original text 27.04
- bugfix (from ver 25.96) no need to exit, restart after update 25.99
- Paradox.net file is always in the Paradox directory. The former unnecessary flexibility
entailed the complication of one extra possible drive and folder dependency. 25.92
- better service detecting switch setting changes at startup 25.73
- Show report bugfix (print preview like feature) find next on tab 25.63
- Locus
- Equine notation ABCDE ... Z alleles generalizes the "Polymarker" type 25.83
- improve locus name guessing (e.g. D2/D21 type distinctions) 25.83
- locus ordering
- alphabetize on End or on Alt-a 25.67
- minor bugfix 25.67
- timing stamps show 1/10th of a second 25.67
- experimental, work-in-progress: Auto-pilot feature runs DNAVIEW without user
interaction 25.62
- allow DNAVIEW to operate from directory level below where DNACFG.SF resides 25.67
- allow accession numbers with 0 sequence part, such as
2003-00000. 25.62
- Ctrl-c accepted as an alternative way to revert to top-level menu 25.51
- Top level menu remembers previous commands 25.51
- Echo user responses in bright yellow letters 25.56
- SNP's implemented in various ways 25.49
- import or type in alleles C, G,
A, T 25.49
- Screen looks for SNP matches 25.49
- Import/Export options accept loci in
a single column (instead of necessarily column pairs) 25.49
- Case (Paternity/Crime/Automatic Kinship)
- Recap cleanup this old almost-forgotten feature 28.78
- (experimental) allow half-integer unknown contributors (as approximation to dropped-out alleles) 28.64
- better treatment of default # of unknowns 28.64
- display raw sizes to see all genetic data for the case (same as display raw sizes
under immigration/kinship) 28.45
- Check genotype consistency; big red warning box if inconsistent. 27.32
- select case Clean up "popular case" number list of deleted cases 27.43
- display prominent warning message for 8 seconds when there are contradictory DNA genotypes. 27.31
- Crime Case, Stain Calculator
- New (blindly) calculate all loci takes the place of user
stepping through the loci. 27.31
- Display warning when hypothesized # of unknowns varies across loci. 27.31
- Don't force user to choose database each time. 27.31
- Allow entry of an expression (i.e. 1/220 for an allele frequency). 27.31
- Skip over Amelogenin or other non-autosomal loci. 27.31
- Case Options option to omit "role names" for kinship cases,
hence when the role
words like "Sibling" are misleading for a case, you can omit them. 27.26
- compute one locus replace and enhances "example your risk!" 27.24
- select case
- bugfix remove defunct case numbers (in case of system reset) when user runs Update 27.11
- The Popular Case feature (PgUp) includes cases mentioned
on the recently examined membrane, or whatever membrane you may choose (via PgUp again). 25.91
- Paternity Case
- Include mutation possibilities if effect > x% new option
to control mutation calculation 28.01
- Show results always to 3 significant figures, consistent with Immigration/Kinship 27.49
- If it looks like there may be an "oddball" mutation, prompt user for the relevant parameter. 27.47
- Check for mother-child sample switch; warn ostentatiously if it seems likely. 27.48
- Paternity Case, calculate report highlights loci for which there was a
mutation calculation (with µ) and/or a motherless calculation (with
-m )
and gives on-screen a count of each. 27.14
- bugfix
revert to the method of version 25.92 of frequency calculation so that an
immigration/kinship calculation of a paternity case can agree exactly with the
Paternity case calculate report calculation. (There was a slight
discrepancy in recent versions because the two situations "tossed" different numbers of
alleles temporarily into the database for frequency calculation.) 27.06
- batch select allow selecting in various convenient ways 25.102
- calculate report bugfix VALUE ERROR 25.94
- calculate report bugfix posting to ASCII file
no longer omits Amelogenin 25.92
- when outputting results to a numbered file whose (DOS)
name would otherwise be too long, truncate the leading digits of the case number.
I.e. the case file for case 200412345 might be R0412345.txt. 25.91
- If the file is not empty, offer to clear it before posting the new results. 25.91
- bugfix correct role descriptions for fatherless output 25.91
- cleanup "Consensus" line when negligible variation 25.87
- Automatic Kinship Case improve navigation; avoid add role
default suggestion 25.91
- list cases
- display includes names, races, amount of data, comments 25.77
- bugfix allow empty list 25.78
- Edit case comment add a comment to a case 25.73
- show role letters in "restrict" screen 25.73
- bugfix disallow empty race list 25.73
- bugfix don't ask race when deleting case 25.73
- insists on a legitimate race list (not just -) 25.56
- calculate report
- bugfix prior probability formatting on short report (Kinship similar) 25.87
- bugfix allele display on "SQL LIMS" paternity report 25.77
- bugfix recognize "toss in" parameter in
Gjertson calculation 25.56
- confidence interval estimates removed. (They are
pointless anyway, and it's nearly
impossible to account for the interacting complications of minimum
frequencies, mutation estimates, and null allele computations.) 25.51
- STR model of mutation implemented (if
elected by options switches & parameter settings) 25.49
- bugfix VALUE ERROR invoking
stain calculator 25.56
- (Case) Options new options
- computer-readable report version, written to file.
Available both for paternity and for kinship 25.56
- If the standard filename includes a number such as C:\reports\kin987.txt
(but not C:\reports\kin987x.txt), substitute the number of the current case
truncated if necessary to conform to the DOS 8+3 file naming rule. 25.62
- "prompt for null" causes calculate report
to ask user for null frequency when homozygote encountered 25.56
- "Ultra-conservative multiple race calculation"
is formerly standard behavior smallest PI locus-by-locus.
If value "no", then use smallest PI overall, but use the same race
for each locus. 25.56
- bugfix can't create cases manually in 25.43 unless
Options Name tag style:
is NAME. 25.46
- Immigration/kinship
- Bayes Calculator new name, formerly Posterior probability 28.46
- Kinship log report documents databases used. 28.46
- Bad bone analysis:
Dropout [NOT] allowed (FOR ROLES __) toggle
to assume dropout for some samples 28.42
- Show pairwise relationships evaluates the following pairwise relationships among
every pair of people in the case: 28.24
- identity / identical twin
- parent-child
- siblingship
- double first cousin
- half sibling (avuncular, grandparental same thing)
- cousin
- Estimate likely relationships
- shows which relation 28.31
- include Y-haplotype 27.51
- Chart of posterior probabilities evaluates posterior probabiities for a range
of prior probabilities, in particular the "requisite prior" corresponding to the specified
posterior threshold if any. 28.24
-
Posterior probabilities interactive chart computes posteriors
from priors, even when multiple (>2) hypotheses are computed. 27.31, 28.24
- X-linked markers (work in progress for now girl can't be homozygous at all loci) 27.14
- enhanced better to integrate Y-haplotype information 27.49
- Simulate, Print summary Include case number and personnel. 27.47
- Estimate relationship includes Y-haplotype 27.51
- Allow summary even when no autosomal data (to allow incorporating Y-data) 27.49
- Symbolic genotype chart includes both autosomal and Y loci 27.49
- Chart of posterior probabilities cleaner 27.49
- Y-haplotype summary compares Y-haplotypes in the case and computes matching odds. 27.47
- Show Y-haplotype in colored letter display 27.51
- Y-haplotype matching odds 27.42
- posterior probability chart per various priors 27.42
- Calculate ... includes a mutation indication even when >2 hypotheses
27.26
- Calculate one locus only show genotypes of
people involved in the scenario for editing 27.25
- "parsing" options Calculate one locus, showing parsing and
Parsing info: SHOWN:
- allow changing any genotype interactively.
Useful for comparison computations to analyze mutation. 27.23
- much clearer & more helpful debugging display 27.23
- (& Kinship) Type in scenario
- input has a memory; PgUp/PgDn
(or Ctrl-Up/Dwn)
to scroll to a previous input scenario. 27.23
- first character typed clears the type-in area; on-screen instructions explain.
(First move with an arrow to avoid this behavior.) 27.16
- cleaner input screen;
allow longer scenarios. (To get extra room for a very long scenario, leave the
type-in screen then re-enter; you'll have three new blank lines at the bottom.)
25.93
- Shortcut keys include copy-and-paste; F1
for keystroke help (left, right-click to copy; ctrl-v to paste) 28.35, 28.42
- allow more attractive alternative statement separators to %: 27.47
symbol | name | method to type |
♦ | diamond
| Alt ~ (note: regardless of key caps, that's Alt with the upper-leftmost key) |
¤ | starburst | Alt shift 8 |
∩ | cap | Alt c |
-
multiple hypotheses [Kinship etc] Case. 27.24 & prev
- When >2 hypotheses, display the LR matrix comparing all possibilities. 27.23
- compares more than two hypotheses simulataneously.
Use the verbose syntax method and prefix the second
alternate hypothesis with two /'s, etc. 27.15
Example:
C:M+F ; primary F is the father
/ C: M+Bro ; alternate F is the uncle
/ Bro,F:?+?
// C:M+? ; second alternate F is unrelated
- restore the Amelogenin display 25.96
- improve "needless loci" option so that needless loci are not displayed 25.96
- improve locus coloring in symbolic genotype display 25.94
- allow empty pedigree 25.94
- preserve the setting for Prior Probability across sessions 25.91, 25.93
- show progress & time 25.92
- simplify report (always include "details" instead of asking) 25.92
- allow lower-case letters to begin a name in the automatic version of Kinship
hence
C:m+F is ok (but m does not mean M ). 25.91
- prominently display settings of the important switches/toggles 25.91
- allow arithmetic expression (e.g. 123/301) when manually specifying
allele frequencies 25.91
- Racial estimate compares racial origins for all profiles in the case 25.85
- cosmetic change 27.21
- select candidate races per Racial distance;
more general combinations allowed 25.93
- easier no need for user to modify Case Options 25.93
- Immigration show & print genotype table options 25.76
- New input notation prefix alternative scenario lines with / 25.67
- Speedups cousin problems and redundant siblings for example 25.67
- Allele painting more informative 25.67
- clarify locus name display 25.92-3
- Logical symbolic allele names: pr
means that the alleles are 2 steps apart, etc 25.67
- ct etc. for SNP's 25.67
- SNPs correctly colored 25.73
- add menu item to change database default selections 25.58
- Improve menu appearance & reword 25.56
- Needless loci option to clean
up display by eliding irrelevant loci 25.56
- Kinship simulation predicts whether a given kinship
problem will be solveable if genetic information becomes available. 25.28
- plays music to alert you when simulation run is done 28.78
- cleaner display of distribution deciles 28.67
- Browse implements a friendly way to return to previous simulations 28.56
- Export all nnn LR's and distribution graph creates
file from which Excel can make a beautiful graph 28.55
- prompts for multiplex instead of aborting if no databases for specified multiplex 27.04
- new options allows simulating completion of partial profiles
(e.g. 13-locus simulation optionally completes 9-locus profiles,
in addition to 13-locus profiles for as yet untyped
people) 25.102
- ask for total simulation count (not incremental) 25.99
- allow simulation prior probability; show average posterier in summary 25.99
- track multiple simulations better 25.99
- Show loci of a multiplex when selecting a multiplex 25.96
- Show the assumed hypothesis prominently if not PRIMARY 25.96
- cosmetic: round more nicely 25.94
- While simulating, keep cumulative results in view; show progress & timing. 25.93
- Allow setting PRIOR from the Simulate menu ~25.97
- If PRIOR>0 (to set it, Esc up one level to Immigration/Kinship),
then the average W-value (posterior probability) will be included in the simulation
report. 25.93
- Cleaner and more general multiplex specification 25.91
- prominently display settings of the important switches/toggles 25.91
- options to record the individual simulations to the long (log) report 25.91
- allow under "Autopilot" control 25.83
- better menu default suggestions 25.91
- much better menu, more options 25.67
- allow defining scenarios in Simulate 25.73
- considerably cleaned up, easier to use 25.56
- enhancements including allowing simulation of a single locus 25.49
- bugfixes
- count number of alternate-hypothesis simulations correctly 27.02
- keep data straight when simulating alternative hypothesis 25.96
- ok to take a scenario from the pick list 25.93
- rare bug with a very large family reported results
like (0+0r)/0r due to incorrect rounding 25.91
Kinship Run test cases includes the
formerly problematic scenario as a test case. 25.91
- give graceful error warning on illegal kinship scenario 25.91
- fix VALUE ERROR 25.78
- sometime types got "stuck", same assignment occurred repetitively 25.56
- remove bias that favored selecting rare alleles for the simulation 25.39
- Improve screen display during simulation. 25.39
- sometimes died listing the assigned alleles. 25.35
- Database /
- Assign race to membrane accepts multiple membrane/worklists
(& option to exclude children) 28.42
- Rare alleles improved analysis, output 25.49
- Printout database rewritten, improved 28.25
- Type in data to create a database, Edit database
- allow entering null (use n) 27.28
- help text sometimes obscured some information. 27.23
- better guessing at database size when you enter frequencies 27.17
- Prompts recall previous answers, more convenient when creating several databases.
27.02
- allow STR data. Long-standing bug didn't allow compilation of imported
data into a database 25.101
- Disaster analysis
- Membrane collapse
- bugfix care against occasional LENGTH ERROR's 27.02
- recognize related profiles by similar core ID # and create a "virtual" profile
as a composite 25.96
- Screen disaster matches
- Screen summary report New computer-friendly summary of the Screening results 27.36
- DNA odds, DNA exclusion, Y-haplotype odds
- Y haplotype odds
- allows # instead of an allele number to select a random allele size.
(Alternatively type a race letter to select random allele from that race.) 28.46
- Fill in all loci by putting # for the locus. 28.28
- caters to partial profiles 27.42
- DNA exclusion odds
- Show exclusion probability as 0.99999999+, never as 1. 28.51
- Allow up to 18 loci 28.28
- option: Show raw size data, Add raw size data to report
auditing aid to see exact input data 27.37
- DNA odds, DNA exclusion remember previous case across sessions
27.26
- give visible feedback on CLEAR and ADD actions 27.18
- DNA odds permits a large number of loci (but
for this version only if you import the profile; can't type it
directly into DNA odds) 25.49
- DNA Profiles
- retain race-theta correspondence accurately 27.02
- better sample name indication, includes case and name/comment 25.87
- collect profile from all relevant membranes 25.87
- bugfix "minimum count" sensitive 25.87
-
- Worklist Sizes simple and useful new command to
display/prepare a report showing the DNA profiles for a selected worklist/membrane 28.46
- Import/Export
- LIMS import allow browsing 27.24
- DNAVIEW frequency database import Multiple file selection treats a response
of ~ alone the same as blank (ignores it). 27.24
- Import ASCII database histogram has
much friendlier dialogue; allows importing many loci from one file (parallel columns;
the column for allele sizes can be shared or can be different for different loci)
27.23
- Genotyper, Genemapper import etc
- interpret underscore ( _ ) as a space in the Sample Info field 28.85
- special format for Lancet 28.78
- New "Select on ..." option allows filtering the input file accepting some samples and discarding others 28.49
- Use the treat-as-null/homozygous Options switch for importing
bones preparatory to kinship bone dropout analysis 28.42
- GeneMapper import can import peak height/area (not used yet though)28.42
- allow comma (,) or slash (/)
as an allele separator 28.16
- excellent import wizard 28.23, 28.31
- Allow importing of a case comment (an input column headed "Comment"). 27.48
- Recognize loci better, e.g. Penta's, Y-loci 27.47
- Reduce chance of user error by not putting a red bar on the list of membranes/worklists. 27.47
- allows (and ignores) leading garbage lines 27.35
- Avoid duplicating computer-assigned accession numbers even if the user accidentally errs 27.17
- When user creates a new membrane (=worklist), use it for import automatically 27.16
- If re-import against a membrane (=worklist) has conflicting roster information protect
the user by aborting the input 27.16
- less confusing display of import report 27.04
- GeneMapper import New option
allows importing the ABI GeneMapper file format of DNA
profiles. Similar to Genotyper import. 27.02
- shorten import dialogue when generating new cases 25.91
- allow blank column heading 25.76
- Don't ask for "configuration"; no longer needed for allele data 25.73
- allow (& ignore) double quotes (") surrounding fields 25.67
- When approving the locus/column name interpretation,
Page Up selects the column with sample information 25.62
- allows single column/locus (space between for STRs, space not needed for
SNP or other 1-letter code alleles) 25.56
- allow (accession number)+(case)+(role) format for Sample Info (experimental) 25.56
- faster for large datasets 25.43
- bugfixes
- avoid INDEX ERROR when adding data to a previous RFLP membrane 25.02
- recognize conflict on newly created numbers 25.67
- allow leading blank lines and column headings 25.67
- allow Esc on membrane select to abort 25.67
- allow duplicated
locus (two instances must non-consecutive) 25.58
- allow blank Amelogenin 25.56
- Import genotypes for database
- Import can treat illegal allele as homozygote.
See Options,
Offladder allele policy 28.42
- improved report on check for duplicate profiles 28.41
- bugfixes
- ellipsis shortcut notation failed if a very large number of loci 27.18
- when choosing a selection phrase don't ignore the last character 27.18
- check for duplicate sample numbers before other checks. 25.91
- better & clearer checking for duplicate and similar databases already present 25.67
- Allow allele notation such as <10 or >22
(which are recorded as 1 and 99 respectively) 25.67
- show allele names properly when comparing new database with old one to replace 25.39
- bugfixes
- correctly report deleted sample number 27.02
- permit homozygous notation 25.83
- compares new versus old correctly when replacing an extant database 25.39
- WTC import cater to VIRT samples 25.67
- Independence of Loci, HW test
- Allow the allele of a homozygous genotypes to be written
either once (e.g. 10) or twice
(e.g. 10 10). 27.02
- bugfix LENGTH error if select no columns, then select
no locus. 27.02
- bugfix allow room to specify shuffling many many columns 25.58
- Kinship
- Maintenance
- network clean up Network Lock Test; show "waiting" box
whenever interlock engaged. 28.15
- locus list by chromosome
Alphabetize list within chromosome. Better user interaction. 27.04
- RecordSwitch allows disabling switch-checking 25.99
- cleanup & minor bugfixes 25.73
- Options
- Offladder allele policy 3rd option:
Ignore illegal notation (treat as null/homozygous). The other two are Discard
the locus (the new option just discards one allele), and Treat as rare. 28.42
- new Options Decimal symbol symbol is . (period per U.S.)
or , (comma per European) 28.34
- Case numbering to allow long (9 digit) case numbers 28.15
- Locus name style like: D16S539
to present shorter version (omit chromosomal info, omit "STR") of locus name for
reports etc. 28.13
- convert accession codes
option for Katrina sample name scheme 27.31
- New option DNAVIEW report includes: [workstation] [version] to enhance
the title line on each printed report 27.06
- DNAVIEW report title line dialogue in a cleaner box 27.06
- Numlock toggle works (finally) 25.99 usually the numlock key itself works anyway 27.01
- Paradox directory
Simpler designation of Paradox repository. The folder (usually
pdox ,
occasionally D:\dnaview\pdox for suitable drive letter if you have a
networked system with customized workstations) needs only to be set here; no longer
need it also be set/changed in the Network tool. This simplification should make
for easier moving of DNAVIEW to a different location, since there is at most
this one place within DNAVIEW with a critical drive letter or full pathname. 25.93
- improve appearance 25.56
- select PCR separator (i.e. 9.3 or 9,3 etc.) 25.56
- character conversion allow nulls 25.56
- Keyboard allows about ten national keyboards 25.56
- bugfix worklist spacing 25.67
- bugfix default date 25.46
-
- Printout database (in Database) optionally show allele probabilities (i.e. taking
into account minimum frequency and add-observed-allele-to-database parameters) and/or
sample frequency. 28.46
- Database similarity test menu simplified including new options Compute p-value for one locus and
Compute individual p-valueS for each locus to help explore data. 28.46
- Y Databases / 28.45
- Y haplotype database statistics under Y databases
shows various statistics of the installed Y-haplotype databases 28.42
- Y-haplotype statistics & analysis bugfixes 28.81
- include "Matching LR for new type" 28.52
- Install Y-haplotype databases from worklist
converts one or several worklists to Y-haplotype database, adds them to the list of Y-haplotype databases 28.45
- Rename, reorder, delete Y-databases 28.45
- Y-haplotype matching odds same as in menu 28.45
- Plot
- reduce number of prompts, more friendly: 28.43
- allele range indicated for the locus as well as for this database 28.43
- METAFIL option nicer 28.43
- Improve display of database names 28.15
- DISPLAY shows diagnostic error code when unable to display 27.11
- fails gracefully with a message when absence of graphics engine makes plotting impossible 27.08
- gives nice preview of STR database. 27.02
- Recognizes Esc to quit. 27.02
- Racial measurement tools
- Racial Distances a new command under Research
Ideas uses whatever loci databases are available for to construct a "mileage
chart" of likelihood-ratio distances among any specified set of races. 25.91
- more flexible; recognizes a set of
databases as pertaining to the race for which they are defined as default
(which the user can easily specify even temporarily), in addition to the race
for which they are defined. 27.23
- Racial estimate compares racial origins for specified profile or case-worth 25.85
- optionally excludes racial mixtures from the report 27.08
- bugfixes
- Case (Paternity, Kinship, Crime) bugfixes
- Paternity Case bugfixes
- Find commment don't crash. 28.57
- Don't consider random man mutation 28.51
- test calculation examples more accurate reference answers 28.51
- don't hold cases so greedily when user departs 28.47
- bug in 28.43 prevented recomputing a case and
re-saving the "standard" report 28.44
- Don't allow calculate paternity unless proper roles are present 28.12
- Don't prompt for "oddball" if the case is obvious exclusion 27.49
- Don't prompt for "oddball" when someone has >2 alleles 27.49
- Don't prompt null frequency unless ASK/AUTO switch is ASK 27.49
- Mother-child sample switch check was wrong in 27.47. 27.48
- handle Amelogenin correctly in fatherless maternity case 27.32
- calculate report error when no loci and no mother 27.16
- mis-sorted the roles in some situation. 27.48
- When entering/editing a person, at the field, hit the DELete key
to remove the race (replaces the race letter with
- ). 27.24
- Immigration/Kinship bugfixes
- Immigration/Kinship posterior probability of 9.8/1 million is 0.001%, not 0.000 28.51
- Simulate bugfixes
- allow consecutive simulations with different multiplexes 28.42
- Simulate correctly when new allele included in profile 28.13 28.25
- skip Y-loci rather than VALUE ERROR 27.07
- allow unseen alleles among given profiles 27.14
- Don't allow "Pat" as mother in one hypothesis, father in another 28.14
- Type in scenariotyping a character after inserting a line doesn't clear the
window 27.28
- Kinship, Immigration/Kinship editing frequencies rarely
crashed DNAVIEW 27.27
- Simulate failed if case included an allele not listed in the database 27.44
- avoid INDEX ERROR if illegal polymarker type
- Case ... more careful display of 99.999...% and similar 27.31
- skip Y-haplotype data 25.92
- Immigration/Kinship skip Amelogenin correctly (27.49 error) 27.53
- repair calculation error of ver 27.26 27.28
- Kinship Run test cases; check program restore cleaner display
27.29
- Print genotypes include size chart when printing 27.07
- frequency calculation
gives error indication if illegal genotype (like 3 alleles) 27.04
- sometimes the DNA profiles shown in the report file
didn't match the heading roles (M, C, etc.) 27.02
- locus name coloring on the colored symbolic genotype
exhibit was sometimes missing when the exhibit was too close to the
bottom of the screen 27.02
- document the case on the (long) report 25.92
- DNA odds/exclusion/Y-haplotype odds bugfixes
- DNA odds allow space to new locus row 28.78
- Y haplotype odds bugfixes
- permit not counting tested profile in database 28.78
- "person" button works now 28.47
- # correctly creates a locus list 28.45
- "experimental calculation" 25.56
- respond correctly to menu choices 28.28
- DNA odds matching odds are 1e6, not 1/1e6 28.15
- DNA exclusion allow printing via Ctrl-enter 27.18
- DNA odds, DNA exclusion wrong frequency calculation if NML mode and window size=0 27.19
- DNA odds, DNA exclusion frequency calculation from wrong locus when changing alleles 27.19
- DNA odds fix INDEX ERROR 25.56
- Import/export bugfixes
- Hitachi Import allow lane number gaps 28.79
- Import Ascii database cleanup wizard;
give error if missing allele designation 28.17
- allow GeneMapper files with no "height" column 28.04
- GeneMapper Import allows (and ignores properly) ID_LADDER 27.39
- Parse Probusqueda File (specific-user feature) accidently
assigned a victim role to a reference 27.21
- other bugfixes, unsorted
|