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README.mkd 2024-09-26 5.6 kB
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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
Source: README.mkd, updated 2024-09-26