Hello everyone,
I was just wondering if anyone had experience with working with variants generated through the torrent variant caller.... I tried measuring genotype concordance between by sequenced data and separate genotype data (for the same sample) and it is very low.... I'm not sure of the sensitivity/specificity of the torrent variant caller.
Any help is appreciated.
I was just wondering if anyone had experience with working with variants generated through the torrent variant caller.... I tried measuring genotype concordance between by sequenced data and separate genotype data (for the same sample) and it is very low.... I'm not sure of the sensitivity/specificity of the torrent variant caller.
Any help is appreciated.