Example:
seq1 AGTC seq2 AGTT seq3 GGGT cons AGTT
The variations are then found by comparing seq1,2 and 3 against the consensus
I just start a mapping-by-sequencing project, but I was confused with consensus call.
In order to find mutation with SHOREmap, I have to provide the SHOREmap extract or SHOREmap backcross with consensus call information. The program tutorial tell me that I should use 11_converted_consen.txt . I want to know what is the definition of *consensus call *.
Is that means the "snp" with many reads supporting?
I find a definition of consensus sequence.
consensus sequence
a sequence of NUCLEOTIDES or AMINO ACIDS that is used to describe a number of related but not identical sequences. It is compiled by inserting the nucleotide occurring most often at each position in the real sequences. -- Collins Dictionary of Biology, 3rd ed. © W. G. Hale, V. A. Saunders, J. P. Margham 2005
So, consensus call is the output produced by consensus caller to find consensus sequences. And we can find variation(such as snp) in this output file.
Example:
seq1 AGTC seq2 AGTT seq3 GGGT cons AGTT
The variations are then found by comparing seq1,2 and 3 against the consensus
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