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Diffstat (limited to 'academic/snpEff/README')
| -rw-r--r-- | academic/snpEff/README | 4 |
1 files changed, 2 insertions, 2 deletions
diff --git a/academic/snpEff/README b/academic/snpEff/README index a32c83dfba..979686a271 100644 --- a/academic/snpEff/README +++ b/academic/snpEff/README @@ -14,11 +14,11 @@ acid changes). This also installs SnpSift, a toolbox that allows you to filter and manipulate annotated files. Once your genomic variants have been -annotated, you need to filter them out in order to find the +annotated, you need to filter them out in order to find the "interesting / relevant variants". Given the large data files, this is not a trivial task (e.g. you cannot load all the variants into XLS spreadsheet). SnpSift helps to perform this VCF file manipulation and -filtering required at this stage in data processing pipelines. +filtering required at this stage in data processing pipelines. If you are using SnpEff or SnpSift, please cite: A program for annotating and predicting the effects of single |