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Contig Ploidy and Allele Dosage Estimation
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gramarga/ConPADE
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###################################################################### # # # ConPADE: Contig Ploidy and Allele Dosage Estimation # # # ###################################################################### # # # Version 1.0-4 # # Last updated: 10/30/2015 # # # ###################################################################### For licensing information, please read file LICENSE.txt distributed with this package ###################################################################### Installing from source: - ConPADE is written in C# and can be built with any compatible compiler (Visual Studio, Xamarin Studio or MonoDevelop) - To compile ConPADE from source, you need to link against the .NET Bio libraries. These can be found at https://github.com/dotnetbio/bio After successfully building the binaries, make sure you also have the error model files (errorModel.bin and substModel.bin) from the main distribution folder. ###################################################################### First steps: To run a sample data set, simply open a command line, navigate to the ConPADE folder and type \YourWorkingDirectory\RunTestData.bat or issue the command \YourWorkingDirectory\ConPADE -bamName TestData.bam Make sure all downloaded files are in the folder. ###################################################################### Result files: Default behavior is to produce three files from the input BAM file. - ploidy: one line per contig, with the second column indicating the most likely ploidy, followed by the log-likelihoods for each evaluated ploidy - readStats: read usage statistics, a table containing information on numbers of aligned reads and base pairs for each contig - SNP: a table with identified variants, one SNP per line Optionally, argument -splitContigs can be used to produce four files for each individual contig. - logLikelihoods: contains log-likelihoods for each evaluated ploidy - ploidy: a single integer indicating the most likely ploidy - readStats: read usage statistics - SNP: a table with identified variants ###################################################################### To get help on usage and detailed information about arguments, open a command line, navigate to the ConPADE folder and type YourWorkingDirectory\ConPADE ###################################################################### Version changes: * 1.0-1 - Using updated .Net Bio version 2.0 to fix BAM parsing - Output is now combined for all contigs (there is an option to split files for individual contigs) - Changed argument from -bamNames to -bamName * 1.0-2 - Bug fix: properly ignore not aligned reads * 1.0-3 - Bug fix: added support for dummy reads in BAM file - Bug fix: hard-clipped sequences are now correctly parsed * 1.0-4 - First source code release - Removed dependency on Escience.dll
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