Massively parallel sequencing of 231 autosomal SNPs with a custom panel

The custom-designed single nucleotide polymorphism (SNP) panel amplified 231 autosomal SNPs in one PCR reaction and subsequently sequenced with massively parallel sequencing (MPS) technology and Ion Torrent personal genome machine (PGM). SNPs were chosen from SNPforID, IISNP, HapMap, dbSNP, and related published literatures. Full concordance was obtained between available MPS calling and Sanger sequencing with 9947A and 9948 controls. Ten SNPs (rs4606077, rs334355, rs430046, rs2920816, rs4530059, rs1478829, rs1498553, rs7141285, rs12714757 and rs2189011) with low coverage or heterozygote imbalance should be optimized or excluded from the panel. Sequence data had sufficiently high coverage and gave reliable SNP calling for the remaining 221 loci with the custom MPS–SNP panel. A default DNA input amount of 10 ng per reaction was recommended by Ampliseq technology but sensitivity testing revealed positive results from as little as 1 ng input DNA. Mixture testing with this panel is possible through analysis of the FMAR (frequency of major allele reads) values at most loci with enough high coverage depth and low level of sequencing noise. These results indicate the potential advantage of the custom MPS–SNP assays and Ion Torrent PGM platform for forensic study

Biology · Computational biology · Concordance · dbSNP · DNA · DNA sequencing · Gene · Genome · Genomics · Genotype · International HapMap Project · Ion semiconductor sequencing · Massive parallel sequencing · Personal genomics · Sanger sequencing · Single-nucleotide polymorphism · SNP · SNP array · SNP genotyping · Environmental DNA in Biodiversity Studies · Forensic and Genetic Research · Molecular Biology Techniques and Applications · Genetics