Entering edit mode
9.7 years ago
phoenixice154
•
0
Dear All,
I am going to try HapTree to phase the SNP/MNP/InDel/Complex in my VCF, and want to give HapTree a try. But I really have no idea how to prepare the reads input (instead of BAM or fragment file) for HapTree v0.1 (as v1 only support diploid). Would someone help?
Here is a part of the format from examples:
{9: 1, 4: 0}
{0: 1, 1: 0, 4: 0}
{8: 1, 4: 0}
{2: 1, 3: 1}
{9: 0, 4: 1}
{2: 0, 3: 0, 5: 1, 6: 0, 7: 1}
{2: 1, 3: 1}
{5: 1, 6: 0, 7: 1}
{3: 1, 5: 0, 6: 1, 7: 0}
{2: 1, 3: 1}
{2: 1, 3: 1, 6: 0, 7: 1}
{2: 0, 3: 0, 5: 1, 6: 0, 7: 1}
{1: 0, 2: 1, 3: 1, 5: 0, 6: 1}
........
What does the number mean? That really needs an good manual for that.
Please help, any idea?
The first number might refer to the Num-th line in VCF, and the second number might refer to the alleles, each line might refers to an alignment?
How to indicate a Paired END?