摘要:
The present invention provides methods of determining a Genetic Composite Index score by assessing the association between an individual's genotype and at least one disease or condition. The assessment comprises comparing an individual's genomic profile with a database of medically relevant genetic variations that have been established to associate with at least one disease or condition.
摘要:
The present invention provides methods of determining a Genetic Composite Index score by assessing the association between an individual's genotype and at least one disease or condition. The assessment comprises comparing an individual's genomic profile with a database of medically relevant genetic variations that have been established to associate with at least one disease or condition.
摘要:
The present disclosure provides methods and systems for incorporating multiple environmental and genetic risk factors into an individual's genomic profile. Methods include assessing the association between an individual's genotype and at least one disease or condition by incorporating multiple genetic risk factors, environmental risk factors, or a combination of both.
摘要:
The present disclosure provides methods and systems for assessing an individual's genotype correlations to a phenotype by analyzing the individual's genomic profile and using ancestral data to determine the correlations between genotypes and phenotypes.
摘要:
The present disclosure provides methods and systems for assessing an individual's genotype correlations to a phenotype by analyzing the individual's genomic profile and using ancestral data to determine the correlations between genotypes and phenotypes.
摘要:
A method of comparing nucleic acid sequences being ESTs included in a first database of sequences and nucleic acid sequences included in a second database of sequences to form groups of sequences from the two databases that all relate to the same gene. For each one or more n-groups of sequences of one of the two databases, associating therewith lists of nucleic acid sequences, each from one of said two databases, each sequence on the list containing the n-groups, and matching sequences on the lists to generate said group.
摘要:
A method of obtaining an mRNA sequence having alternative spliced variants from a database of ESTs, comprising: providing a raw database comprising a plurality of ESTs; and assembling ones of said ESTs into mRNA sequences, wherein said assembling includes identifying alternative spliced regions.