Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes
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Updated
May 16, 2024 - C
Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes
Please switch to https://github.com/OpenGene/defastq
Process Illumina instrument data into SAM/BAM/CRAM files.
check paired-end FASTQ data integrity
Targeted Fusion Caller (C)
Illumina (and SOLiD) sensitive read mapping tool (cloned from svn://scm.gforge.inria.fr/svnroot/storm/)
A sequence-read simulator program for NGS
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