METHOD, DEVICE, AND MEDIUM FOR RESULT PREDICTION FOR ANTIBODY SEQUENCE

    公开(公告)号:US20230343412A1

    公开(公告)日:2023-10-26

    申请号:US18058611

    申请日:2022-11-23

    发明人: Fei YE Danqing WANG

    IPC分类号: G16B20/30 G16B20/50

    CPC分类号: G16B20/30 G16B20/50

    摘要: Systems and methods directed to providing a method for determining a prediction result related to an antibody sequence. The method comprises obtaining an antibody sequence comprising a plurality of amino acids, and obtaining a germline sequence of the antibody sequence. The method further comprises determining a prediction result related to the antibody sequence based on at least one of: evolution information between the antibody sequence and the germline sequence, or a mutation position on the antibody sequence, wherein an amino acid of the plurality of amino acids mutates on the mutation position.

    NON-ANIMAL HUMAN RELEVANT WORKSTATION SYSTEM AND METHOD FOR TESTING NEUROVIRULENCE AND NEUROTOXICITY IN VACCINES

    公开(公告)号:US20230298694A1

    公开(公告)日:2023-09-21

    申请号:US17722528

    申请日:2022-04-18

    摘要: A system and method for test predicting human neurovirulence and neurotoxicity risks is disclosed. The system comprises a real-time platform or TRANS-MSC (Configured Human induced Pluripotent Stem Cells) unit and a trained digital platform. The TRANS-MSC incubates the vaccine/biologic, drug/API, cosmetic/ingredient, anti-venom aliquots collected from the produced batches in the manufacturing system. The digital platform is embedded with artificial intelligence (AI) and machine learning (ML) modules, augmented with a robotic process automation framework. The AI modules predict human neurovirulence, human neurotoxicity patterns along with any adventitious microbial contaminants in the process. The AI and ML modules are trained with a plurality of TRANS-MSC acquired phenotype micrographs and a plurality of neurotoxic genes involved in viral, bacterial, fungal infections. Further, the test is customized to a genetically distinct population, user’s library of research-grade, ingredients, intermittents, final products, etc. that are at the risk of causing neurovirulence or neurotoxicity in the clinics.

    METHOD FOR GENERATING VARIANTS OF A PROTEIN
    6.
    发明公开

    公开(公告)号:US20230227534A1

    公开(公告)日:2023-07-20

    申请号:US17631640

    申请日:2020-07-24

    发明人: Patrick BARTH

    摘要: The present disclosure relates to a method for generating variants of a protein based on a native protein regulated by allosteric pathway, the method comprising:

    i) providing 3D structures of the native protein;
    ii) identifying at least one pair of coupled allosteric sites within the amino acid sequence of the native protein named microswitch;
    iii) generating in silico mutations of said identified microswitch to generate a pool of variants;
    iv) computing at least one score reflecting the variation in allosteric coupling; and/or the variation in the relative stability
    v) predicting the activity of each variant compared to the native protein based on the computed score.

    The disclosure also concern a computer implemented program to carry out said method, and a variant of a protein or an active fragment thereof, a polynucleotide.

    SYSTEMS AND METHODS FOR USE IN IDENTIFYING MULTIPLE GENOME EDITS AND PREDICTING THE AGGREGATE EFFECTS OF THE IDENTIFIED GENOME EDITS

    公开(公告)号:US20220361428A1

    公开(公告)日:2022-11-17

    申请号:US17874203

    申请日:2022-07-26

    摘要: Methods are provided for genome editing. On example method includes editing a genome sequence of an organism with multiple edits simultaneously without precise knowledge of a phenotypic effect of each individual one of the multiple edits, wherein the multiple edits are selected based on a prediction of an aggregate phenotypic effect of the multiple edits on a phenotypic trait. The method also includes aggregating the multiple edits into multi-dimensional pools, whereby phenotypic effects of contrasting pools of edits are compared to ascertain which of the multiple edits are most likely to be causing large phenotypic effects while eliminating need to evaluate each edit separately. The organism may include one of: maize, soybean, wheat, sorghum, rice, cotton, rapeseed, sunflower, bean, tomato, squash, cucumber, melon, pepper, watermelon, eggplant, okra, pea, chickpea, lentil, peanut, onion, carrot, celery, beet, cauliflower, broccoli, cabbage, Brussels sprout, radish, black-eyed pea, potato, sweet-potato, sugar cane, cassava, and banana.

    Methods for Rule-based Genome Design

    公开(公告)号:US20220246240A1

    公开(公告)日:2022-08-04

    申请号:US17719431

    申请日:2022-04-13

    摘要: Methods and systems for designing, testing, and validating genome designs based on rules or constraints or conditions or parameters or features and scoring are described herein. A computer-implemented method includes receiving data for a known genome and a list of alleles, identifying and removing occurrences of each allele in the known genome, determining a plurality of allele choices with which to replace occurrences in the known genome, generating a plurality of alternative gene sequences for a genome design based on the known genome, wherein each alternative gene sequence comprises a different allele choice, applying a plurality of rules or constraints or conditions or parameters or features to each alternative gene sequence by assigning a score for each rule or constraint or condition or parameter or feature in each alternative gene sequence, resulting in scores for the applied plurality of rules or constraints or conditions or parameters or features, scoring each alternative gene sequence based on a weighted combination of the scores for the plurality of rules or constraints or conditions or parameters or features, and selecting at least one alternative gene sequence as the genome design based on the scoring.