|
Preclinical work-up
From
each family, heterozygous STR markers, closely linked with
the HLA genes, presenting alleles not shared by the parents
are selected. The aim is to select markers as much as
possible evenly spaced throughout the HLA complex, so that
an accurate mapping of the whole region could be achieved.
The optimization of the multiplex PCR protocol is performed
on the couples' own single lymphocytes, determining the best
condition to obtain reliable and reproducible results from
single cell amplification.
The number of markers/loci included in the first round
multiplex PCR varies from 14 (in cases without testing for a
causative gene) to 22 (including in the reaction HLA STR
markers, gene regions involved by mutation, STR markers to
these regions and STR markers used for aneuploidy
detection).
Parameters such as amplification efficiency and allele
drop-out (ADO) rate for each marker used in the multiplex
PCR is also determined prior to apply the protocol to the
clinical cases.
Next :
Genetic Testing
|