Abstract: Methods, systems, and computer-readable media for intelligent license management are disclosed. A renewal date, complexity level, and contact information for a plurality of licenses is received and stored in a database, and a table comprising this information is generated and stored in the database. A reminder date for each of the plurality of licenses is determined based on the renewal date and complexity level and stored in the table in association with a corresponding license of the plurality of licenses. It is subsequently determined when a current date corresponds to the reminder date for a license, and a notification is automatically transmitted to a user associated with the contact information for the at least one license. The notification is configured to be displayed on a graphical user interface with a selectable link which when selected, causes display of the table.

Abstract: A system for providing intervention information to a subject may be configured to perform a method including: receiving, via the processor, genetic information of the subject, the genetic information including a plurality of sets, and each set comprising one or more genes; assigning, via the processor, a value to each respective set; assigning, via the processor, a respective classification to the subject in one or more categories, wherein: each category corresponds to a respective set; and the assignment of the respective classification is based on the respective values assigned to the respective sets; obtaining, via the processor, health profile information and wellness intervention information associated with the assigned classifications of the one or more categories; and outputting, via the processor, the health profile information and the wellness intervention information to a user.

Abstract: Systems and method for performing a genotype-based analysis of an individual are discussed. An exemplary method may include: causing an interactive interface of an assessment application operating on a user device to prompt for responses to one or more phenotype interrogatories from an individual; receiving, from the user device, responses to the one or more phenotype interrogatories from the individual, entered via the interactive interface; using a relational model, determining at least one genotype classification for the individual based on the received responses to the one or more phenotype interrogatories; and causing the interactive interface to output information associated with the at least one genotype classification.

Abstract: Methods for preparing recombinant proteins, such as antibodies, in eggs are described. The method offers advantages over existing systems for preparing recombinant proteins including high yield, low cost and compatibility with animal protection regulations. In addition, since eggs are edible food sources the recombinant protein does not have to be isolated from the egg.

Abstract: Methods for preparing recombinant proteins, such as antibodies, in eggs are described. The method offers advantages over existing systems for preparing recombinant proteins including high yield, low cost and compatibility with animal protection regulations. In addition, since eggs are edible food sources the recombinant protein does not have to be isolated from the egg.

Abstract: Methods for preparing recombinant proteins, such as antibodies, in eggs are described. The method offers advantages over existing systems for preparing recombinant proteins including high yield, low cost and compatibility with animal protection regulations. In addition, since eggs are edible food sources the recombinant protein does not have to be isolated from the egg.

Abstract: Compilations of nucleic acids, articles of manufacture which are surfaces comprising multiple blocks of arrays comprising such compilations, methods of use of the compilations and arrays for detection of chromosomal disorders, such as a chromosomal aneuploidies, deletions, amplifications, and diagnosis and prognosis of syndromes associated with a contiguous gene abnormality and kits are provided.

Abstract: Compilations of nucleic acids, articles of manufacture which are surfaces comprising multiple blocks of arrays comprising such compilations, methods of use of the compilations and arrays for detection of chromosomal disorders, such as a chromosomal aneuploidies, deletions, amplifications, and diagnosis and prognosis of syndromes associated with a contiguous gene abnormality and kits are provided.

Abstract: Disclosed are methods for identifying genetic mosaicisms in cell populations. Suitable cell populations include, e.g., biopsy or body fluid samples or cultures of cancer cells. The method includes performing array-based comparative genomic hybridization (CGH), wherein a plurality of cloned genomic nucleic acid segments is provided in a plurality of identical replicas, each cloned segment immobilized to a discrete and known spot on a substrate surface to form the array, and the cloned genomic nucleic acid segments comprise a substantially complete first genome of a known first karyotype. The invention also provides methods for optimizing performance of an array-based comparative genomic hybridization (CGH).

Abstract: In one aspect the invention provides compilations of nucleic acids, articles of manufacture, e.g., arrays, and methods for the detection of chromosomal abnormalities, such as a chromosomal aneuploidies, deletions, amplifications, and the like, and the diagnosis or prognosis of syndromes associated with a contiguous gene abnormality. Kits are also provided.

Abstract: The present invention provides comparative genomic hybridization methods for detecting and mapping chromosomal or genetic abnormalities associated with various diseases or with predisposition to various diseases, or to detecting the phenomena of large scale copy number variants. The method includes hybridization with one or more probes for detecting balanced translocations. Such probes may be complementary to the moving genomic segment which is translocated or may be complementary to the translocation break point.

Abstract: Described is a nucleic acid-containing substrate that is useful for nucleic acid hybridization methods, such as methods that utilize nucleic acid microarrays. The substrate contains nucleic acid that had not been covalently modified prior to having been contacted with the substrate and/or nucleic acid that is bound substantially non-covalently to the substrate. The nucleic acid remains associated with and/or bound to the substrate even after high stringency washings. Also described is a method for preparing the nucleic acid-containing substrate and methods for using the nucleic acid-containing substrate to detect or quantitate a target nucleic acid.

Abstract: The present invention provides methods of detecting and mapping chromosomal or genetic abnormalities associated with various diseases or with predisposition to various diseases, or to detecting the phenomena of large scale copy number variants. In particular, the present invention provides advanced methods of performing array-based comparative hybridization that allow reproducibility between samples and enhanced sensitivity by using the same detectable label for both test sample and reference sample nucleic acids. Invention methods are useful for the detection or diagnosis of particular disease conditions such as cancer, and detecting predisposition to cancer based on detection of chromosomal or genetic abnormalities and gene expression level. Invention methods are also useful for the detection or diagnosis of hereditary genetic disorders or predisposition thereto, especially in prenatal samples.

Abstract: Methods for preparing recombinant proteins, such as antibodies, in eggs are described. The method offers advantages over existing systems for preparing recombinant proteins including high yield, low cost and compatibility with animal protection regulations. In addition, since eggs are edible food sources the recombinant protein does not have to be isolated from the egg.

Abstract: Compilations of nucleic acids, articles of manufacture which are surfaces comprising multiple blocks of arrays comprising such compilations, methods of use of the compilations and arrays for detection of chromosomal disorders, such as a chromosomal aneuploidies, deletions, amplifications, and diagnosis and prognosis of syndromes associated with a contiguous gene abnormality and kits are provided.

Abstract: Methods for preparing recombinant proteins, such as antibodies, in eggs are described. The method offers advantages over existing systems for preparing recombinant proteins including high yield, low cost and compatibility with animal protection regulations. In addition, since eggs are edible food sources the recombinant protein does not have to be isolated from the egg.

Abstract: The invention provides arrays comprising a plurality of biological molecules, wherein each biological molecule is immobilized to a discrete and known spot on a substrate surface to form an array of biological molecules, and each biological molecule comprises a detectable label. The invention provides a multiplexed system for performing comparative genomic hybridization (CGH) using an array of the invention. The invention also provides methods of making and using these arrays, including a method of comparing copy numbers of unique nucleic acid sequences in a sample.

Abstract: In one aspect the invention provides compilations of nucleic acids, articles of manufacture, e.g., arrays, and methods for the detection of chromosomal abnormalities, such as a chromosomal aneuploidies, deletions, amplifications, and the like, and the diagnosis or prognosis of syndromes associated with a contiguous gene abnormality. Kits are also provided.

Abstract: The invention provides array-based methods for determining genetic mosaicisms in cell populations, such as biopsy or body fluid samples or cultures of cancer cells. The invention also provides methods for optimizing performance of an array-based comparative genomic hybridization (CGH).

Abstract: The invention provides novel methods to map the location and measure the expression of some or all the genes expressed by a cell using array-based nucleic acid hybridizations. The use and applicability of the invention includes identification of tissue specific genes and identifying different tissue types during growth and development. The methods also can be used to identify genes expressing abnormal types of transcripts or abnormal levels or transcripts. Thus, the invention can be used to identify genes encoding transcripts associated with disease processes, such as cancer.