190940 ⎘
Systems and methods for genomic variant annotation
#902Biological sample measuring apparatus
#903ELECTRONIC VARIANT CLASSIFICATION
#904SYSTEMS AND METHODS FOR DISEASE ASSOCIATED HUMAN GENOMIC VARIANT ANALYSIS AND REPORTING
#905Using RNAi imaging data for gene interaction network construction
#906Combining RNAi imaging data with genomic data for gene interaction network construction
#907Combining RNAi imaging data with genomic data for gene interaction network construction
#908Methods to determine carcinogenesis, identify markers for early cancer diagnosis and identify targets of therapy
#909Methods for analyzing blood to detect diseases associated with abnormal protein aggregation
#910Using RNAi imaging data for gene interaction network construction
#911DIAGNOSING AND MONITORING DEPRESSION DISORDERS
#912CHARACTERIZING UNCHARACTERIZED GENETIC MUTATIONS
#913METHOD AND KIT FOR CHARACTERIZING MICROORGANISMS
#914Method and kit for characterizing microorganisms
#915Methods, systems, and software for identifying functional bio-molecules
#916GENETIC VARIANTS ON CHR 11Q AND 6Q AS MARKERS FOR PROSTATE AND COLORECTAL CANCER PREDISPOSITION
#917Method for evaluating drug sensitivity and disease vulnerability by analyzing cyclic AMP responsive element binding protein gene
#918Metaproteomic Method to Identify Secreted Pattern Recognition Molecules and Adhesive Antimicrobial Factors for Detection of Microbial Agents Eliciting Inflammation in the Human Host
#919Patient stratification and determining clinical outcome for cancer patients
#920Molecular profiling of tumors
#921METHODS AND PROCESSES FOR NON INVASIVE ASSESSMENT OF A GENETIC VARIATION
#922METHOD FOR PROCESSING GENOMIC DATA
#923METHODS FOR ESTIMATING GENOME-WIDE COPY NUMBER VARIATIONS
#924Detection of genetic or molecular aberrations associated with cancer
#925GENETIC MARKERS FOR RISK MANAGEMENT OF ATRIAL FIBRILLATION, ATRIAL FLUTTER, AND STROKE
#926System and Methods for Pharmacogenomic Classification
#927Molecular profiling of tumors
#928Molecular profiling of tumors
#929Methods, systems, and software for identifying bio-molecules using models of multiplicative form
#930Systems and methods for genetic data compression
#931Methods, systems, and software for identifying bio-molecules with interacting components
#932Identifying interacting DNA loci using a contingency table, classification rules and statistical significance
#933SYSTEM AND METHOD FOR ANALYZING UNI- OR MULTI-VARIATE DATASETS
#934Grouping system using genotype-based SNS
#935Feature selection for efficient epistasis modeling for phenotype prediction
#936Feature selection for efficient epistasis modeling for phenotype prediction
#937Haplotying of HLA loci with ultra-deep shotgun sequencing
#938Stable gene targets in breast cancer and use thereof for optimizing therapy
#939Identifying antigen clusters for monitoring a global state of an immune system
#940SYSTEMS AND METHODS FOR IDENTIFYING THE RELATIONSHIPS BETWEEN A PLURALITY OF GENES
#941Noninvasive prenatal molecular karyotyping from maternal plasma
#942Partition defined detection methods
#943SYSTEM AND METHOD FOR CLEANING NOISY GENETIC DATA FROM TARGET INDIVIDUALS USING GENETIC DATA FROM GENETICALLY RELATED INDIVIDUALS
#944DNA MATCHING
#945High-resolution melting analysis
#946Diagnosis, prognosis and identification of potential therapeutic targets of multiple myeloma based on gene expression profiling
#947Artificial Intelligence System for Genetic Analysis
#948Genetic, metabolic and biochemical pathway analysis system and methods
#949Molecular profiling of tumors
#950Cost-optimized design analysis for rapid microbial prototyping
#951HIV INCIDENCE ASSAYS WITH HIGH SENSITIVITY AND SPECIFICITY
#952MOTIF FINDING PROGRAM, INFORMATION PROCESSOR AND MOTIF FINDING METHOD
#953Compositions and methods for identifying and comparing members of microbial communities using amplicon sequences
#954Analysis of DNA samples
#955Processing data from genotyping chips
#956Assessment of cellular signaling pathway activity using probabilistic modeling of target gene expression
#957Molecular profiling of tumors
#958Molecular profiling of tumors
#959Methods for non-invasive prenatal ploidy calling
#960System and method for determining individualized medical intervention for a disease state
#961Biomarkers For Predicting Progressive Joint Damage
#962Method for identifying antibiotic targets
#963Methods for quantifying nucleic acid variations
#964Method for identifying antibiotic targets by complemented sequencing
#965VALIDATION OF GENETIC TESTS
#966Methods, Systems and Devices Comprising Support Vector Machine for Regulatory Sequence Features
#967SYSTEM AND METHOD FOR ALIGNING GENOME SEQUENCE
#968SYSTEM AND METHOD FOR DETERMINING INDIVIDUALIZED MEDICAL INTERVENTION FOR A DISEASE STATE
#969Drug discovery methods
#970System and methods for detecting genetic variation
#971System and method for genotyping using informed error profiles
#972System and method for determining individualized medical intervention for a disease state
#973SYSTEMS AND METHODS OF SELECTING COMBINATORIAL COORDINATELY DYSREGULATED BIOMARKER SUBNETWORKS
#974Method of evaluating fatty liver related disease, fatty liver related disease-evaluating apparatus, fatty liver related disease-evaluating method, fatty liver related disease-evaluating program product, fatty liver related disease-evaluating system, information communication terminal apparatus, and method of searching for prophylactic/ameliorating substance for fatty liver related disease
#975Systems and methods for determining the probability of a pregnancy at a selected point in time
#976Information processing system using nucleotide sequence-related information
#977SYSTEM AND METHOD FOR GENOTYPE ANALYSIS AND ENHANCED MONTE CARLO SIMULATION METHOD TO ESTIMATE MISCLASSIFICATION RATE IN AUTOMATED GENOTYPING
#978CROSS-MODAL APPLICATION OF COMBINATION SIGNATURES INDICATIVE OF A PHENOTYPE
#979Compressed Sensing for Simultaneous Measurement of Multiple Different Biological Molecule Types in a Sample
#980Method of measuring a fractional concentration of tumor DNA
#981Method for determining fetal chromosomal abnormality
#982Universal method to determine real-time PCR cycle threshold values
#983siRNA targeting TIE-2
#984Method and system for knowledge pattern search and analysis for selecting microorganisms based on desired metabolic property or biological behavior
#985Evaluating genetic disorders
#986System and method for cleaning noisy genetic data from target individuals using genetic data from genetically related individuals
#987Size-based genomic analysis
#988Systems and methods for identifying sequence variation associated with genetic diseases
#989Methods for the analysis of dissociation melt curve data
#990Ancestral-specific reference genomes and uses thereof
#991SNP detection by melt curve clustering
#992Systems and methods for characterization of molecules
#993Visualization tool for qPCR genotyping data
#994Identifying location biomarkers
#995Techniques for determining haplotype by population genotype and sequence data
#996Determining percentage of fetal DNA in maternal sample
#997System and method for determining individualized medical intervention for a disease state
#998SYSTEMS AND METHODS FOR ANTIBODY ENGINEERING
#999System and method for cleaning noisy genetic data and determining chromosome copy number
#1000GENE-WIDE SIGNIFICANCE (GWIS) TEST: NOVEL GENE-BASED METHODS FOR THE IDENTIFICATION OF GENETIC ASSOCIATIONS HAVING MULTIPLE INDEPENDENT EFFECTS
#1001METHOD FOR DISCOVERING PHARMACOGENOMIC BIOMARKERS
#1002Hierarchical genome assembly method using single long insert library
#1003Physiological signal quality classification for ambulatory monitoring
#1004METHOD FOR DETERMINING THE EFFICACY OF A COMBINATION THERAPY
#1005Comprehensive FMR1 genotyping
#1006Noninvasive prenatal genotyping of fetal sex chromosomes
#1007METHODS FOR GENETIC ANALYSIS
#1008Using lexical analysis and parsing in genome research
#1009Using lexical analysis and parsing in genome research
#1010Healthcare analysis stream management
#1011POPULATION BASED METHOD OF EVALUATING GENOMIC SEQUENCES
#1012METHODS FOR THE SURVEY AND GENETIC ANALYSIS OF POPULATIONS
#1013METHODS FOR THE SURVEY AND GENETIC ANALYSIS OF POPULATIONS
#1014Generating epigenetic cohorts through clustering of epigenetic surprisal data based on parameters
#1015Minimization of epigenetic surprisal data of epigenetic data within a time series
#1016SUMMARIZING AN AGGREGATE CONTRIBUTION TO A CHARACTERISTIC FOR AN INDIVIDUAL
#1017METHOD AND DEVICE FOR ASSEMBLING GENOME SEQUENCE
#1018Diagnosis, prognosis and identification of potential therapeutic targets of multiple myeloma based on gene expression profiling
#1019Mass-spectral method for selection, and de-selection, of cancer patients for treatment with immune response generating therapies
#1020Diagnosing and monitoring CNS malignancies using MicroRNA
#1021COMPUTERIZED METHOD AND SYSTEM FOR INFERRING GENETIC FINDINGS FOR A PATIENT
#1022Methods for diagnosing and treating systemic lupus erythematosus
#1023Method For Integrated Pathology Diagnosis And Digital Biomarker Pattern Analysis
#1024VARIANT ANNOTATION, ANALYSIS AND SELECTION TOOL
#1025Methods for increasing genetic progress in a line or breed of swine using sex-selected sperm cells
#1026Systems and methods for identifying cosmetic agents for hair/scalp care compositions
#1027Reducing sequence read count error in assessment of complex genetic variations
#1028Multivariate genetic evaluation of maize for grain yield and moisture content
#1029Signatures and determinants associated with cancer and methods of use thereof
#1030Determination of the depth coverage of the fetal genome
#1031Method for determining ploidy of a cell
#1032METHODS FOR PRODUCING A HYBRID SEED PRODUCT
#1033Processes for calculating phased fetal genomic sequences
#1034Comprehensive analysis pipeline for discovery of human genetic variation
#1035Diagnosing cancer using genomic sequencing
#1036Systems and Methods for the Analysis of Proximity Binding Assay Data
#1037Method for identifying activation of transferases
#1038VARIABILITY SINGLE NUCLEOTIDE POLYMORPHISMS LINKING STOCHASTIC EPIGENETIC VARIATION AND COMMON DISEASE
#1039METHODS FOR GENETIC ANALYSIS
#1040Genetic Variants as Markers for Use in Urinary Bladder Cancer Risk Assessment, Diagnosis, Prognosis and Treatment
#1041Methods and processes for non-invasive assessment of genetic variations
#1042Methods and apparatuses for predicting risk of prostate cancer and prostate gland volume
#1043METHOD TO DETERMINE AND CORRECT BASELINE AND TO CHARACTERIZE PCR AMPLIFICATION KINETICS
#1044Identifying and correcting an allelic ladder signal for DNA analysis
#1045AI for relating herbal ingredients to illnesses classified in traditional chinese medicine/TCM using probabilities and a relevance index
#1046Methods and processes for non-invasive assessment of genetic variations
#1047System for Identifying Connections Between Perturbagens and Genes Associated with a Skin Hyperpigmentation Condition
#1048Method of constructing a data architecture
#1049Method of formulating a skin-lightening composition
#1050Identifying a de novo fetal mutation from a maternal biological sample
#1051System and method for cleaning noisy genetic data from target individuals using genetic data from genetically related individuals
#1052VACCINES
#1053SYSTEM AND METHOD FOR FACILITATING NETWORK-BASED TRANSACTIONS INVOLVING SEQUENCE DATA
#1054Methods for analyzing massively parallel sequencing data for noninvasive prenatal diagnosis
#1055Methods and devices for single-molecule whole genome analysis
#1056GENE CLUSTER, GENE SEARCHING/IDENTIFICATION METHOD, AND APPARATUS FOR THE METHOD
#1057Size-based analysis of fetal or tumor DNA fraction in plasma
#1058Genome-phenome analyzer and methods of using same
#1059Systems and methods for rational selection of context sequences and sequence templates
#1060Compositions, methods and kits for diagnosis of lung cancer
#1061Genomic features associated with epigenetic control regions and transgenerational inheritance of epimutations
#1062Methods for allele calling and ploidy calling
#1063Compositions, methods and kits for diagnosis of lung cancer
#1064siRNA targeting myeloid differentiation primary response gene (88) (MYD88)
#1065Method for preparing a counter-tagged population of nucleic acid molecules
#1066Amino Acid Sequence Analyzing Method and Amino Acid Sequence Analyzing Apparatus
#1067Methods of Detecting Prenatal or Pregnancy-Related Diseases or Conditions
#1068Measurement and comparison of immune diversity by high-throughput sequencing
#1069Systems and methods for detecting the presence of a biological status using clustering
#1070Determination of gene expression levels of a cell type
#1071SYSTEMS AND METHODS FOR CANCER-SPECIFIC DRUG TARGETS AND BIOMARKERS DISCOVERY
#1072Systems and methods for personalized de-risking based on patient genome data
#1073Systems and methods for using adverse event data to predict potential side effects
#1074Systems and methods for identifying unknown drug targets via adverse event data
#1075PRECISION PHENOTYPING USING SCORE SPACE PROXIMITY ANALYSIS
#1076METAPROTEOMIC METHOD FOR DIAGNOSIS OF BACTERIURIA, UROGENITAL TRACT AND KIDNEY INFECTIONS FROM URINARY PELLET SAMPLES
#1077Methods for non-invasive prenatal ploidy calling
#1078Noninvasive detection of fetal aneuploidy in egg donor pregnancies
#1079Process and system for analyzing the expression of biomarkers in a cell
#1080Systems and methods for medical data processing and analysis
#1081Structure-activity relationships
#1082Systems and methods for identifying drug targets using biological networks
#1083Embedded Data DNA Sequence Security System
#1084METHOD FOR DETECTING GENE REGION FEATURES BASED ON INTER-ALU POLYMERASE CHAIN REACTION
#1085Method and apparatus for mobile disaster victim identification
#1086Secondary structure defining database and methods for determining identity and geographic origin of an unknown bioagent thereby
#1087METHOD AND DEVICE FOR OPTIMIZING A NUCELOTIDE SEQUENCE FOR THE PURPOSE OF EXPRESSION IN A PROTEIN
#1088Engineering surface epitopes to improve protein crystallization
#1089System and method for automated biological cell assay data analysis
#1090Method and system for the use of biomarkers for regulatory dysfunction in disease
#1091Generate percentage of positive cells for biomarkers by normalizing and autothresholding the image intensity produced by immunohistochemistry technique
#1092Methods of protein evolution
#1093Biological information processing method and device, recording medium and program
#1094Prediction device, prediction method, program, and recording medium
#1095PATHWAY ANALYSIS FOR PROVIDING PREDICTIVE INFORMATION
#1096Method and system for phasing individual genomes in the context of clinical interpretation
#1097Methods and processes for non-invasive assessment of genetic variations
#1098SYSTEM AND METHOD OF DETECTING AND CORRECTING FOR NUCLEIC ACID DAMAGE
#1099Systems and methods for interpreting a human genome using a synthetic reference sequence
#1100Method, an arrangement and a computer program product for analysing a biological or medical sample
#1101Identification of conserved peptide blocks in homologous polypeptides
#1102Determination of copy number variations using binomial probability calculations
#1103Analyzing genome sequencing information to determine likelihood of co-segregating alleles on haplotypes
#1104Phasing of heterozygous loci to determine genomic haplotypes
#1105Identifying components of a network having high importance for network integrity
#1106Sequence based engineering and optimization of single chain antibodies
#1107Technique for identifying association variables
#1108Methods of associating an unknown biological specimen with a family
#1109Density based clustering for multidimensional data
#1110Multiplexed digital assays with combinatorial use of signals
#1111Method for determining risk of diabetes
#1112Methods for detecting and treating systemic lupus erythematous
#1113Systems and methods for detecting the presence of a biological status using plot
#1114Method of identifying peptides
#1115Determining analyte concentrations in biological fluids with abnormal output detection
#1116Methods for non-invasive prenatal ploidy calling
#1117Resolving genome fractions using polymorphism counts
#1118Precursor selection using an artificial intelligence algorithm increases proteomic sample coverage and reproducibility
#1119Scar-less multi-part DNA assembly design automation
#1120Computer systems for annotation of single molecule fragments
#1121System and method for analyzing DNA mixtures
#1122System, method, and computer software product for genotype determination using probe array data
#1123Systems and methods for detecting biological features
#1124Methods for identifying DNA copy number changes
#1125Method for identifying peptides and proteins from mass spectrometry data
#1126Risk calculation for evaluation of fetal aneuploidy
#1127Compensation for spectral crosstalk in multiplex nucleic acid amplification
#1128Methods for increasing genetic gain in a breeding population
#1129Mobile biometrics information collection and identification
#1130Method and system for knowledge pattern search and analysis for selecting microorganisms based on desired metabolic property or biological behavior
#1131Computer implemented methods of treating lung cancer
#1132Prediction of phenotypes and traits based on the metabolome
#1133Cooperation-based method of managing, displaying, and updating DNA sequence data
#1134Device and method for comparing molecular signatures
#1135Methods for estimating genome-wide copy number variations
#1136Compositions and methods for prediction of drug sensitivity, resistance, and disease progression
#1137Method and system for determining whether a drug will be effective on a patient with a disease
#1138Target-specific non-antibody protein and method for preparing the same
#1139Attribute combination discovery for predisposition determination
#1140Bambam: parallel comparative analysis of high-throughput sequencing data
#1141Automated analysis of multiplexed probe-target interaction patterns: pattern matching and allele identification
#1142Compositions and methods for discovery of causative mutations in genetic disorders
#1143Device and method for selecting genes and proteins
#1144Methods for predicting stability and melting temperatures of nucleic acid duplexes
#1145miRNA target prediction
#1146Probes and methods for determining the presence or absence of genetic segments
#1147Data analysis and predictive systems and related methodologies
#1148Computer system and microfluidic instrumentation for next-generation biological signaling network research and applications
#1149Base sequence cluster generating system, base sequence cluster generating method, program for performing cluster generating method, and computer readable recording medium on which program is recorded and system for providing base sequence information
#1150GENETIC POLYMORPHISMS ASSOCIATED WITH STATIN RESPONSE AND CARDIOVASCULAR DISEASES, METHODS OF DETECTION AND USES THEREOF
#1151Differential filtering of genetic data
#1152Method for judging risk of cancer recurrence, computer program, and computer system
#1153System and method for targeting relevant research activity in response to angiogenic regulator analyses
#1154Comparative genomic hybridization array method for preimplantation genetic screening
#1155System and method for statistical mapping between genetic information and facial image data
#1156Identification and modification of dynamical regions in proteins for alteration of enzyme catalytic effect
#1157Predicting response to chemotherapy using gene expression markers
#1158Protein engineering
#1159Methods, systems, and software for identifying functional bio-molecules
#1160Competitive inhibitors of invariant chain expression and/or ectopic clip binding
#1161Copy number analysis of genetic locus
#1162Physiogenomic method for predicting drug metabolism reserve for antidepressants and stimulants
#1163Receptor modulators
#1164Methods for determining correlated residues in a protein or other biopolymer using molecular dynamics
#1165Lipid tumour profile
#1166Evaluating genetic disorders
#1167Application of machine learning methods for mining association rules in plant and animal data sets containing molecular genetic markers, followed by classification or prediction utilizing features created from these association rules
#1168Devices for continual monitoring and introduction of gastrointestinal microbes
#1169System and method for editing and manipulating DNA
#1170Assessment of physiological conditions
#1171Method and system for determining whether a drug will be effective on a patient with a disease
#1172Genetic analysis systems and methods
#1173Interactive genome browser
#1174Determining a probabilistic diagnosis of autism by analysis of genomic copy number variations
#1175Method and kit for dynamic gene expression monitoring
#1176Diagnosis, prognosis and identification of potential therapeutic targets of multiple myeloma based on gene expression profiling
#1177Methods for assembling panels of cancer cell lines for use in testing the efficacy of one or more pharmaceutical compositions
#1178Individualized cancer treatment
#1179HIV-1 reverse transcriptase codon deletion and its use in the management and treatment of HIV infections
#1180Compositions and methods for therapeutic delivery with frozen particles
#1181Methods and systems for assessment of clinical infertility
#1182Lung cancer evaluating apparatus, method, system, and program and recording medium therefor
#1183Categorization and filtering of scientific data
#1184Complex formation method and separation method
#1185Family inheritance
#1186Biological dataset profiling of cardiovascular disease and cardiovascular inflammation
#1187Genetic comparisons between grandparents and grandchildren
#1188Methods for identifying DNA copy number changes using hidden markov model based estimations
#1189Side effects prediction using co-associating bioattributes
#1190Methods for selecting initial doses of psychotropic medications based on a CYP2D6 genotype
#1191Modulation of chemosensory receptors and ligands associated therewith
#1192Computational method and apparatus for predicting polypeptide aggregation or solubility
#1193Methods, apparatus, and computer programs for verifying the integrity of a probe
#1194Method for the spectral identification of microorganisms
#1195Methods, systems, and software for identifying functional biomolecules
#1196Apparatus, compositions, and methods for assessment of chronic obstructive pulmonary disease progression among rapid and slow decline conditions
#1197Systems for arbitrary peptide synthesis
#1198Methods, apparatus, and computer programs for verifying the integrity of a probe
#1199Shift-invariant predictions
#1200Methods, systems, and software for identifying functional biomolecules