All blood samples were amplified directly without DNA extraction. The 268 unrelated samples were genotyped using our new established multiplex amplification system on the Thermo 96-Well PCR System (Thermo Fisher Scientific Company, Carlsbad, United States). The analyzed panel including 38 X-InDel markers, namely rs10671504, rs11277082, rs1160845, rs143123845, rs149102585, rs16367, rs16368, rs16397, rs16637, rs17394, rs199731653, rs2307707, rs2307741, rs2308033, rs2308280, rs25581, rs3048996, rs3077884, rs3215490, rs34763847, rs35574346, rs35954471, rs363794, rs4030406, rs45449991, rs56820033, rs57608175, rs57843641, rs58595330, rs59605609, rs60283667, rs71671860, rs3216913, rs10699224, rs3859989, rs61260787, rs36094418 and rs79829945. The localizations of the different markers were previously described in our published article (Chen et al., 2021 (link)). Separation of PCR-amplified products were performed on the ABI 3130xL DNA Analyzer (Applied Biosystems, Foster City, CA, United States). Electropherogram analysis and allele assignment were performed with GeneMapper v 4.0.
Free full text: Click here