Abstract: A method, system, and apparatus for determining paternity based on eye color. Determining paternity may include accessing a color digital image of at least one of a male parental candidate, a female parental candidate, and a child candidate. An eye color of each of the male parental candidate, the female parental candidate, and the child candidate may be determined, wherein the eye color of at least one of the male parental candidate, the female parental candidate, and the child candidate is determined based on the accessed color digital image. A paternity likelihood of the male parental candidate with regard to the child candidate may be determined based on the determined eye color of the male parental candidate, the female parental candidate, and the child candidate.

Abstract: A specimen collection and transport kit comprising an external housing member for receiving a tray. A tray comprising a plurality of compartments for receiving a plurality of specimen handling tools and at least one opening configured to receive a specimen container in an upright position during use. Methods for handling a biological specimen including arranging a specimen container in an upright orientation within a tray and transferring a portion of the specimen between one or more receptacles. The methods may be used, for example, to collect and transport urine for urinalysis to diagnose a sexually transmitted disease.

Abstract: Methods useful for multiplex amplifying a plurality of loci or genetic systems comprise at least two loci. The at least two loci may be selected from the group consisting of D9S302, D22S683, D18S535, D3S2387, D4S2366, D5S1719 and D7S1804 loci. In another embodiment, preferably at least two loci comprise complex tandem repeat (CTR) sequences. The methods, kits, compositions and ladders disclosed herein are useful for analyzing human samples, as well as samples from other species. Analysis includes parentage, forensic, tissue origin, sample origin and genetic relatedness studies.

Abstract: A method of ensuring that each newborn infant is identified at birth and maintaining the correct newborn and mother pairing at least until discharge of the mother and child. The method involves genotyping the infant and/or birth mother at one or more times.

Abstract: A method of ensuring that each newborn infant is identified at birth and maintaining the correct newborn and mother pairing at least until discharge of the mother and child. The method involves genotyping the infant and/or birth mother at one or more times.

Abstract: The present invention describes a process of DNA typing performed on human specimens utilizing a specific multiplex reaction which amplifies GATA short tandem repeats in the loci D18S535, D22S683, and D9S302 for the purpose of producing STR genotypes which may be used for identification purposes. This multiplex is an improvement over existing multiplex amplifications for STR typing in that it possesses an extremely high individualization potential for forensic studies and power of exclusion for parentage testing.