Thus, on a per locus basis, sequencing of haplotypes of close SNPs can yield more information than sequencing a single SNP. The question is whether a sufficient number of appropriate haplotype loci can be identified. The value of a locus for identifying familial MEK inhibitor side effects relationships, i.e., lineage informativeness, is related to the number of alleles in the relevant population [26]. Multiple alleles make it less likely two unrelated individuals share both alleles by chance. The more heterozygous a locus, the greater is the chance that the

relevant alleles are uncommon in general but more likely to be found among close relatives than among random or unrelated individuals. More reliable inferences about the degree of relatedness of two individuals are possible if more markers are used. In their review, Weir et al. [26] concluded “It seems that 50 SNPs are insufficient and that 200 SNPs or more will be needed to characterize relatedness.”

For large datasets containing many hundreds of DNA markers quite sophisticated methods of inferring familial relationships have been developed [27]. However, smaller numbers of loci can be used if the loci are sufficiently Lumacaftor nmr heterozygous with multiple alleles. The standard set of CODIS STRPs can be quite useful in this regard because of their multiple alleles but currently they are most reliably genotyped using capillary electrophoresis (CE) while new technology argues for DNA sequencing as a general platform for all forensically relevant markers. Our objective is to validate the use of sequencing for familial searching (and other forensic questions) by identifying a large number of SNP-based, multi-allelic haplotype loci that can be typed by DNA sequencing. To

be appropriate for determining phase by sequencing, we are currently focusing on microhaplotype loci (microhaps) Teicoplanin with extents of 200 base pairs (bp) or less. The potential value of microhaplotypes [23] and [28] and the new results presented here document our progress to find, select, and validate microhaplotype loci for forensic work. A minimum criterion for a microhaplotype locus is at least three haplotypes (alleles) within a region smaller than 200 bp. We have arbitrarily used 200 bp as a current upper limit; this is within the current read length of “desktop” sequencers such as the Ion Torrent PGM sequencer. Regions with a recombination hot spot within that 200 bp must be excluded but very rare historical recombination events will not detract from the general ability to assume identity by descent within a family.