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mrFAST: Our default Illumina read mapper that finds both indels and mismatches and performs iterative search to increase mapping sensitivity. Specifically designed for copy number variation and structural variation analysis.
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mrsFAST: Our alternative Illumina read mapper that finds only mismatches to increase mapping speed. Also supports bisulfite mapping.
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drFAST: Read mapper for di-base color-space reads generated with the SOLiD platform.
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NovelSeq: Novel sequence insertion discovery framework.
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SCALCE: Tool for compression of FASTQ files.
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SPLITREAD: Detection of structural variants and indels from genome and exome sequencing data
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VariationHunter: Structural variation calling algorithm using read pairmapping information including suboptimal alignments.