Merge pull request #152 from WGLab/fiximageInReadme

Fiximage in readme
WGLab · Oct 18, 2016 · dc7f462 · dc7f462
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-![SeqMule](doc/img/seqmule.png)
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 # SeqMule: Automated human exome/genome variants detection
 
 SeqMule takes single-end or paird-end FASTQ or BAM files, generates a script consisting of more than 10 popular alignment, analysis tools and runs the script line by line. Users can change the pipeline or fine-tune the parameters by modifying its configuration file. SeqMule also has some built-in functions, such as pooling consensus calls from various callers, plotting a Venn diagram showing intersection among different callers, and downloading databases. SeqMule can be used for both Mendelian disease study and cancer genome study.

diff --git a/img/seqmule.png b/img/seqmule.png