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Old 03-23-2012, 09:28 PM   #1
Location: Seoul

Join Date: Jan 2012
Posts: 42
Post SIFT - how recognize reference seq?

1. when predicting nsSNV, how can the tools recognize the reference sequence? the reference file in program or input sequence i gave?

i'm doing research about normal-tumor cancer sequence comparison,

and i'm planning to input normal base as reference and tumor base as input data at each position where i'm interested in.

2. is there any other good idea or tools for analyzing Normal-Tumor pair sequence?

HELP!!!! please
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