Name | Modified | Size | Downloads / Week |
---|---|---|---|
README.mkd | 2024-09-26 | 5.6 kB | |
XLibraryDisplay2.48B.xlsm | 2018-04-30 | 949.9 kB | |
example.zip | 2017-10-21 | 6.2 MB | |
XLibraryDisplay2.40B.xlsm | 2017-10-21 | 841.0 kB | |
XLibraryDisplay2.32B.xlsm | 2017-05-20 | 958.3 kB | |
XLibraryDisplay2.16B.xlsm | 2016-09-22 | 935.4 kB | |
XLibraryDisplayManual.pdf | 2015-12-28 | 1.3 MB | |
XLibraryDisplay2.00B.xlsm | 2015-12-14 | 1.1 MB | |
XLibraryDisplay1.81B.xlsm | 2015-10-03 | 907.4 kB | |
XLibraryDisplay1.76B.xlsm | 2015-08-01 | 815.6 kB | |
XLibraryDisplay1.66B.xlsm | 2015-03-06 | 711.7 kB | |
Totals: 11 Items | 14.7 MB | 2 |
XLibraryDisplay: A sequence analysis tool for protein engineering
Website: http://sourceforge.net/projects/xlibrarydisplay
Publication: http://pubs.acs.org/doi/abs/10.1021/ci500362s
For bugs, feedback, and suggestions please email the author at the address found in the publication or manual.
Release Version Notes
2.48
- Improved multicolor SAR map
- Makes back-up of Aligned sheet when clones are removed
- Liability analysis includes polyspecificity motifs (Kelly et JMB 2017)
- Improved stability of contig assembly
- Fixed issue with loading trace/FASTQ files (@ can now begin quality score)
2.40
- Load sequences & QC data from trace (.ab1/.abi/.scr/.ztr) & FASTQ files (.fq/.fastq)
- Calculates hydrophobicity scores
- Limits crashing when run over a network
- Fixed issues with name matching during concatenation and contig assembly
2.32
- Improved integration with Chromas 2.6.3+ -- syncs position & reading frame
- Multi-colored DNA QC using same color scheme as Chromas
- Contig assembly of overlapping DNA sequences
- Merge\Concatenate non-overlapping sequences
- Matched pair analysis to identify mutations that correlate with activity
- Highlights unusual antibody residues
- Remove clones by right-clicking on Antibody sheet
- Local sequence comparison pop-up after similarity calculation
- Sequence motifs on composition sheet
- Color all\Mutations colors mutations in orange
- Faster TrimmedQC consensus DNA calculation
- Properly counts Ns in consensus TrimmedQC DNA sequence
- Verifies FASTA format for protein sequences to prevent crashing
- Fixed transfer of color from Aligned to Antibody sheets
2.16
- View chromatograms -- right-click to open trace(s) in Chromas/ChromasPro/FinchTV
- New sequence analysis files can be merged with prior analysis files
- Annotates antibody side-chains as buried/exposed
- SAR map to identify mutations that correlate with activity
- Option to highlight mutant Cys residues
- Sort aligned sequences by Cys total
- Auto-trim template with ORF Finder
- Revised context-sensitive tips
- Drop-down menu for DNA QC assignments
- Send feedback and re-filter buttons added
- Export .ARFF files for Weka and .CSV files for R
- Friendly warning if important sheets are edited
- Standard sheets automatically re-added if user deletes them
- Fixed display issues with Local DNA/AA alignment and ORF Viewer
2.00
- Major interface improvement with custom ribbon
- Icons added to right-click menu
- Added start page and revised the Template sheet
- Abbreviated DNA analysis and right-click menus
- Antibody annotation improved and better integrated
- Automatically mark antibody CDRs as library residues
- Segments statistics and trimming DNA made optional
- Option to convert Aligned template to consensus sequence
- Color all amino acids on the aligned sheet
- Sort by name, sequence, annotation, and mutations
- Sort by essentially unlimited library residues
- Option to auto-pick unique leads by the entire sequence
- Export sequences from the summary sheet
- Right-click to view translated ORFs
- Fixed bug with Phred QC analysis of reverse complements
- Fixed bug showing control data in certain cases
1.81
- DNA template or proteins can be entered directly or by copy/paste
- Template creation tools including ORF finder and viewer
- Faster Phred file loading and similarity plot creation
- Fixed problems with using multiple drives
- Small interface adjustments
1.76
- Protein sequences can be loaded directly
- ClustalW2 and MAFFT can be used for alignment
- Faster Needleman-Wunsch alignment
- Mutations can be colored by physicochemical differences
- Summary enabled for all or just library residues
- Sorting no longer necessary before counting uniques
- Inconsistent gaps do not affect counting of unique clones
- Streamlined message boxes
- Coloring after sorting made optional
- Reasons on BadDNA sheet moved to column D
- Fixed bug in PyMOL script with mutation selection
- Other small stability improvements
1.66
- Adds reasons on BadDNA sheet for removing clones
- User can annotate reasons for manually removing clones
- Log sheet automatically records program and user actions
- Auto-pick sheet format revised
- Standard worksheets renamed automatically to prevent crashes
- Properly counts undetermined codons
- More stability improvements
1.62
- Improved activity data handling:
- Allows missing data points
- Clones with missing data can be excluded
- Sequence correlation with non-numeric data enabled
- Identifies missing activity headings and sample IDs
1.61
- Can ignore data columns when excluding by activity
- Can exclude sequences if data for clones is not found
- Auto-removes empty rows & columns on Activity sheet
- Printable alignment properly copies cell borders
- Fixed search by name
1.60
- Consensus sequences now shown on TrimmedQC sheet
- Minor bug fixes
1.59
- More intuitive filtering options
- Advanced filtering options with Phred QC data
- FASTA or raw sequences can now be exported
- Abort buttons added to simple and NW alignments
- Stability improvements
- Minor GUI modifications
1.58
- First version after publication
- Added more coloring to TrimmedQC sheet
- Activity data optional check set to 1000 sequences