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Changelog.md

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Changes:

version modifications
v1.1.0 + added strandedness information for single exon genes
+ fixed GUI rules for CRISPRa/i
+ added option so TSS are only counted if belonging to the gene of interest
+ changed bowtie off-target mode to -k ( offtargets allowed +1 ) so that bowtie always searches if designs have less or at least on off-target more than allowed. This way, sgRNAs are excluded which do have more than the allowed off-targets and included if less. Earlier one could allow more off-targets then bowtie was searching for.
v1.2.0 + fixed overlapping criterion to beeing 3 bp downstream of the PAM (sgRNAend - 5bp)
v1.3.0 + fixed error in version 1.2 where filter criteria like exons were not interpreted
+ enabled automated deletion of single gene files in the server appliation so only the usmmary is kept
+ fixed all binary builds
v1.3.1 + fixed error in version 1.3.0 where gene names with underscores caused major trouble
v1.4.0 + removed html output option
+ fixed alignment match coordinates to be according to unspecific leading base pairs
+ added the columns, Chromosome, Match-Chromosome, Start_rti, End_rti (relative to input)
+ fixed Manual and Readme for the new cloumn headings
+ fixed sgRNA ranking accordingly
v1.4.1 + fixed a problem when purpose was set to non-coding so that not all possible sgRNA were considered for the library fitering
v1.4.3 + Added TTTV as PAM
+ fixed output fasta file when PAM is 5'
v1.4.4 + fixed 5_prime PAM matchstring
+ fixed 5_prime PAM off-target behaviour
+ changed off-targets-allowed parameter to targets-allowed the number has to be greater than 1. Else all sgRNAs are excluded also those that only have one "on-target"
v1.4.5 + fixed error handling with doubled gene ids. Now a warning is thrown and genes are processed in alphanumerical order
+ fixed issues when Genes had similar names with numerics e.g. RPL3 and RPL30
+ fixed counting of missing genes
v1.4.6 + fixed an issue with library output in fasta format, where only the PAM was in the output oligo