Summary of the variant filtering process.
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The number of variants after each of the filtering steps is shown for the 9 non-BRCA1/2 families. The original SNPs were matched against the control pool as well as with the other member/s of the family. Previously undescribed variants were then selected and consequences obtained using PerlAPI tools. Intronic consequences were discarded and finally the variants were checked for homology. *with respect to SNPs shared by family.
创建时间：
2010-04-02
