Dear colleague,
I have a question regarding Phred. If you have a base from a sequencing
read that has a designated Phred score of 20 and the equivalent base
from the complementary strand also has a designated score of 20, what
would be the confidence value in a concensus built from these two
strands ??
Given that each base has at Phred 20, by definition, a 1% chance of
being wrong is the error rate for the resulting concensus 1% of 1%, in
other words 1 in 10,000 that is q40 ?? If not how is the resulting Phred
score computed ??
Thanks for any assistance
Laurence Hall
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Laurence S Hall
Senior Research Associate
Rubicon Genomics
Suite G
4370 Varsity Drive
Ann Arbor
MI 48108
US
Tel. : (00) 1 734 677 2793
Cell : (00) 1 734 727 5140
Fax : (00) 1 734 477 9902/3
EMail : hall at rubicongenomics.comlhall48108 at yahoo.com
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