Cohort selection with privacy protection

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The 23Andme, Inc. patent solves the following problem:

Now, clinical target specific genetic factors in human subjects research is often made to attract candidates who have a certain genetic condition through special pools (eg, patient groups), screening for particular genotypes studied, and the selection of members based on screening results. The selection process tends to be difficult for several reasons. First, a large number of candidates often need to recruit. To help these people, to make them interested in studying, and getting them to sign on to be expensive and time consuming. Second, all the candidates have to be screened to determine if they have a specific genetic condition, which is an expensive and laborious process. For study of rare genetic conditions in particular, many iterations will be needed to achieve a significant population study.

Our analysis of this patent is as follows:

23Andme, Inc.’s patent US 8990250 B1 deals with Cohort selection with privacy protection.
Assembling a band include: receiving the genetic nature of information concerning a desired genetic traits; the use of genetic traits to seek information in a data store containing information previously genotyped individuals to take a group of candidates with the desired genetic traits; and gathering battalion based at least in part the group of candidates.

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Processing data from genotyping chips

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The 23Andme, Inc. patent solves the following problem:

The instructions for making cells in the human body is encoded in deoxyribonucleic acid (DNA). DNA is a long, ladder-shaped molecule, each equivalent to climb up on a pair of interlocking units, called bases, appointed by the four letters of DNA AlphaBeta, T, G and C. a always pairs or chains with T, and G always pairs or chains with C. the order of these four letters in one DNA called human genome.

Our analysis of this patent is as follows:

23Andme, Inc.’s patent US 8645343 B2 deals with Processing data from genotyping chips.
Processing genetic data disclosed, including: receiving two or more gene sets of data for an individual from the source of one or more of the gene data; combining the genetic data sets from one or more genetic data sources, including the recognition of a copy SNP among the genetic data set and determine the one or more data values ​​stored for duplicate SNP; and storing a set of Merged genetic data for the individual.

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Genotype calling

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The 23Andme, Inc. patent solves the following problem:

The instructions for making cells in the human body is encoded in deoxyribonucleic acid (DNA). DNA is a long, ladder-shaped molecule, each equivalent to climb up on a pair of interlocking units, called bases, appointed by the four letters of DNA AlphaBeta, T, G and C. a always pairs or chains with T, and G always pairs or chains with C. the order of these four letters in one DNA called human genome.

Our analysis of this patent is as follows:

23Andme, Inc.’s patent US 8428886 B2 deals with Genotype calling.
Determine a genetic sequence for a particular place in the genome of a man declared, including: receiving a measure associated with a particular file for the particular on the human genome, to receive contextual information associated with a context of individual within a larger collection of genetic information, and the use of measures associated with particular order -is and contextual information to calculate an improved determination of genetic sequences to particular parts of the human genome.

The revolutionary TRAN&ASSOCIATES provides patent creation and management tools to help inventors protect their inventions using the patent system. Full lawyer support to complete and file the application is available.