SINGLE TUBE QUANTITATIVE POLYMERASE CHAIN REACTION (PCR)

METHOD FOR ASSEMBLING SEQUENCED SEGMENTS

Direct identification and measurement of relative populations of microorganisms with direct DNA sequencing and probabilistic methods

Intermittent detection during analytical reactions

METHODS AND SYSTEMS FOR PREDICTIVE MODELING OF HIV-1 REPLICATION CAPACITY

ALLELIC DISCRIMINATION ANALYSIS USING AN EFFICIENCY RELATED VALUE (EFR)

CONSIDERATION OF EVIDENCE

SYSTEM AND METHOD FOR ALIGNING GENOME SEQUENCE

Secure Informatics Infrastructure for Genomic-Enabled Medicine, Social, and Other Applications

SYSTEM AND METHOD FOR ALIGNING GENOME SEQUENCE CONSIDERING REPEATS

SYSTEM AND METHOD FOR ALIGNING GENOME SEQUENCE CONSIDERING ENTIRE READ

SYSTEM AND METHOD FOR ALIGNING GENOME SEQUENCE

Classification of nucleotide sequences by latent semantic analysis

MOLECULAR FINGERPRINTING TO IDENTIFY INBREEDING AND OUTBREEDING DEPRESSIONS

System and methods for detecting genetic variation

Genome explorer system to process and present nucleotide variations in genome sequence data

System and method for propagating information using modified nucleic acids

METHODS AND SYSTEMS FOR IDENTIFYING, FROM READ SYMBOL SEQUENCES, VARIATIONS WITH RESPECT TO A REFERENCE SYMBOL SEQUENCE

Information processing system using nucleotide sequence-related information

Methods and processes for non-invasive assessment of genetic variations

INFORMATION PROCESSING SYSTEM USING NUCLEOTIDE SEQUENCE-RELATED INFORMATION

NUCLEIC READS ALIGNING DEVICE AND ALIGNING METHOD THEREOF

Methods for non-invasive prenatal ploidy calling

Method for determining fetal chromosomal abnormality

Association of data to a biological sequence

System and method for cleaning noisy genetic data from target individuals using genetic data from genetically related individuals

Non-invasive determination of methylome of fetus or tumor from plasma

Secure and scalable mapping of human sequencing reads on hybrid clouds

SINGLE DONOR VERSUS ELITE PANEL METHODOLOGY FOR IDENTIFICATION OF MARKER-ASSISTED BREEDING FRIENDLY MARKERS

Method and apparatus for performing similarity searching

Method of evaluating genomic sequences

SNP detection by melt curve clustering

Nucleic Acid Information Processing Device and Processing Method Thereof

METHOD OF SIMULTANEOUSLY EVALUATING MULTIPLE GENOMIC SEQUENCES

Methods for sequencing polynucleotides

POLYNUCLEOTIDE BASE SEQUENCE DETERMINATION METHOD AND POLYNUCLEOTIDE BASE SEQUENCE DETERMINATION DEVICE

SYSTEMS AND METHODS FOR IDENTIFYING A CONTRIBUTOR'S STR GENOTYPE BASED ON A DNA SAMPLE HAVING MULTIPLE CONTRIBUTORS

Systems and Methods for Detecting Homopolymer Insertions/Deletions

SYSTEMS AND METHODS TO DETECT COPY NUMBER VARIATION

IDENTIFICATION AND USE OF BACTERIAL [2Fe-2S] DIHYDROXY-ACID DEHYDRATASES

Single Nucleotide Polymorphism Biomarkers for Diagnosing Autism

Determining percentage of fetal DNA in maternal sample

RAPID METHOD OF PATTERN RECOGNITION, MACHINE LEARNING, AND AUTOMATED GENOTYPE CLASSIFICATION THROUGH CORRELATION ANALYSIS OF DYNAMIC SIGNALS

GENERATION AND REPRODUCTION OF DNA SEQUENCES AND ANALYSIS OF POLYMORPHISMS AND MUTATIONS BY USING ERROR-CORRECTING CODES

Detecting and classifying copy number variation

METHOD OF CORRELATED MUTATIONAL ANALYSIS TO IMPROVE THERAPEUTIC ANTIBODIES

MAPKAP kinase-2 as a specific target for blocking proliferation of P53-defective

Identification and use of bacterial [2Fe-2S] dihydroxy-acid dehydratases

ESTIMATION OF RECENT SHARED ANCESTRY

DETERMINING A PROBABILISTIC DIAGNOSIS OF CANCER BY ANALYSIS OF GENOMIC COPY NUMBER VARIATIONS

Methods and systems for determining haplotypes and phasing of haplotypes

Using lexical analysis and parsing in genome research

Using lexical analysis and parsing in genome research

Statistical inspection systems and methods for components and component relationships

Healthcare analysis stream management

Systems and methods for processing nucleic acid sequence data

Methods and processes for non-invasive assessment of genetic variations

Systems and methods for run-time sequencing run quality monitoring

Assembly of metagenomic sequences

Reducing sequence read count error in assessment of complex genetic variations

NORMALIZING CHROMOSOMES FOR THE DETERMINATION AND VERIFICATION OF COMMON AND RARE CHROMOSOMAL ANEUPLOIDIES

Determination of the depth coverage of the fetal genome

Methods, computer-accessible medium, and systems for score-driven whole-genome shotgun sequence assembly

METHODS FOR DETERMINING ABSOLUTE GENOME-WIDE COPY NUMBER VARIATIONS OF COMPLEX TUMORS

Comprehensive analysis pipeline for discovery of human genetic variation

System and method for generation and use of optimal nucleotide flow orders

Diagnosing cancer using genomic sequencing

Methods and compositions for analyzing nucleic acid

METHODS AND PROCESSES FOR NON-INVASIVE ASSESSMENT OF GENETIC VARIATIONS

METHODS OF CHARACTERIZING, DETERMINING SIMILARITY, PREDICTING CORRELATION BETWEEN AND REPRESENTING SEQUENCES AND SYSTEMS AND INDICATORS THEREFOR

Transmission and compression of genetic data

Random estimation in positron emission tomography with tangential time-of-flight mask

Models for analyzing data from sequencing-by-synthesis operations

Alternative nucleic acid sequencing methods

SYSTEM, METHOD AND COMPUTER PROGRAM FOR NON-BINARY SEQUENCE COMPARISON

Method and System for Accurate Construction Of Long Range Haplotype

Rapid High Resolution, High Throughput RNA Structure, RNA-Macromolecular Interaction, and RNA-Small Molecule Interaction Mapping

GENETIC VARIANTS USEFUL FOR RISK ASSESSMENT OF THYROID CANCER

SYSTEMS AND METHODS FOR IDENTIFYING SOMATIC MUTATIONS

SYSTEM AND METHOD FOR DETERMINING A NUCLEOTIDE SEQUENCE

SYSTEM AND METHODS FOR INDEL IDENTIFICATION USING SHORT READ SEQUENCING

Parallelization of surprisal data reduction and genome construction from genetic data for transmission, storage, and analysis

GENETIC VARIANTS AS MARKERS FOR USE IN DIAGNOSIS, PROGNOSIS AND TREATMENT OF EOSINOPHILIA, ASTHMA, AND MYOCARDIAL INFARCTION

Identifying a de novo fetal mutation from a maternal biological sample

Diagnosis of lymphoid malignancies and minimal residual disease detection

System and method for cleaning noisy genetic data from target individuals using genetic data from genetically related individuals

Using dotplots for comparing and finding patterns in sequences of data points

Methods for analyzing massively parallel sequencing data for noninvasive prenatal diagnosis

ACCURATE COMPARISON AND VALIDATION OF SINGLE NUCLEOTIDE VARIANTS

Novel Restriction Endonucleases, DNA Encoding These Endonucleases and Methods for Identifying New Endonucleases with the Same or Varied Specificity

System and method for processing genome sequence in consideration of seed length

Size-based analysis of fetal or tumor DNA fraction in plasma

Systems and methods for rational selection of context sequences and sequence templates

METHODS FOR ACCURATE SEQUENCE DATA AND MODIFIED BASE POSITION DETERMINATION

Genomic features associated with epigenetic control regions and transgenerational inheritance of epimutations

System and method for processing reference sequence for analyzing genome sequence

Query sequence genotype or subtype classification method

External files for distribution of molecular diagnostic tests and determination of compatibility between tests

ALGORITHMS FOR SEQUENCE DETERMINATION

Method and apparatus for compressing and decompressing genetic information obtained by using next generation sequencing (NGS)

Measurement and comparison of immune diversity by high-throughput sequencing

Identifying randomly distributed microparticles in images to sequence a polynucleotide

Methods and Systems for Medical Sequencing Analysis

SYSTEMS AND METHODS FOR THE DETERMINATION OF A COPY NUMBER OF A GENOMIC SEQUENCE

Systems for and methods of hybrid pyrosequencing

Noninvasive detection of fetal aneuploidy in egg donor pregnancies

Suppression of non-specific amplification with high-homology oligonucleotides

NUCLEIC ACID SEQUENCE ANALYSIS

Systems and methods for step discontinuity removal in real-time PCR fluorescence data

METHOD AND SYSTEM FOR SEQUENCE CORRELATION

Method for identifying nucleotide sequence, method for acquiring secondary structure of nucleic acid molecule, apparatus for identifying nucleotide sequence, apparatus for acquiring secondary structure of nucleic acid molecule, program for identifying nucleotide sequence, and program for acquiring secondary structure of nucleic acid molecule

Method and system for determining the accuracy of DNA base identifications

Method for molecular genealogical research

Compositions and methods for identifying the essential genome of an organism

High efficiency gene transfer and expression in mammalian cells by amultiple transfection procedure of MAR sequences

Methods for treating Barrett's metaplasia and esophageal adenocarcinoma

ALGORITHMS FOR SEQUENCE DETERMINATION

METHOD AND SYSTEM FOR DETECTING REGULATORY SINGLE NUCLEOTIDE POLYMORPHISMS

Compression of genomic data

System and method to correct out of phase errors in DNA sequencing data by use of a recursive algorithm

Method and apparatus for mobile disaster victim identification

Processing and Analysis of Complex Nucleic Acid Sequence Data

Dehalogenases, nucleic acids encoding them and methods for making and using them

Systems and methods for identifying an individual

Identification of DNA fragments and structural variations

DETECTING AND CLASSIFYING COPY NUMBER VARIATION

COMPOSITIONS AND METHODS FOR PROVIDING HEMATOPOIETIC FUNCTION

Method for rapid assessment of similarity between sequences

Method and system for phasing individual genomes in the context of clinical interpretation

Systems and methods for interpreting a human genome using a synthetic reference sequence

Method, system and apparatus to predict and/or recognize and/or classify biological sequences

Physicochemical (PCP) based consensus sequences and uses thereof

Identification of conserved peptide blocks in homologous polypeptides

Analyzing genome sequencing information to determine likelihood of co-segregating alleles on haplotypes

System and method for correcting primer extension errors in nucleic acid sequence data

Phasing of heterozygous loci to determine genomic haplotypes

Field-based similarity search system and method

Detecting and classifying copy number variation

Means and methods for non-invasive diagnosis of chromosomal aneuploidy

Sequence assembly and consensus sequence determination

Methods for placing, accepting, and filling orders for products and services

Polymerase preference index

Resolving genome fractions using polymorphism counts

Scar-less multi-part DNA assembly design automation

Biological data networks and methods therefor

Methods, systems, and computer readable media for nucleic acid sequencing

Virus discovery by sequencing and assembly of virus-derived siRNAS, miRNAs, piRNAs

Methods of identifying an organism

Method and systems for processing polymeric sequence data and related information

Method and systems for processing polymeric sequence data and related information

Method and systems for processing polymeric sequence data and related information

Method and systems for processing polymeric sequence data and related information

Target-specific non-antibody protein and method for preparing the same

Bambam: parallel comparative analysis of high-throughput sequencing data

Bambam: parallel comparative analysis of high-throughput sequencing data

Method and arrangement for the control of measuring systems, corresponding computer program and corresponding computer-readable storage medium

Pair character string retrieval system

Adaptive processing for sequence alignment

Systems and methods for sequence data alignment quality assessment

Antisense transcriptomes of cells

Stabilized polypeptide compositions

Base 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

Identification of ribosomal DNA sequences

Computational methods for translating a sequence of multi-base color calls to a sequence of bases

Modeling of mPGES-1 three-dimensional structures: applications in drug design and discovery

Methods, systems, and software for identifying functional bio-molecules

System and method for monitoring audience in response to signage

Sequence calibration method and sequence calibration device

Capture primers and capture sequence linked solid supports for molecular diagnostic tests

Oligomer sequences mapping

Nucleic acid sequencing system and method

System and method for editing and manipulating DNA

Indexing a reference sequence for oligomer sequence mapping

Systems and methods for identifying replikin scaffolds and uses of said replikin scaffolds

Programmable iterated elongation: a method for manufacturing synthetic genes and combinatorial DNA and protein libraries

Method for identifying peptides using tandem mass spectra by dynamically determining the number of peptide reconstructions required

Using dotplots for comparing and finding patterns in sequences of data points

Lung cancer evaluating apparatus, method, system, and program and recording medium therefor

Categorization and filtering of scientific data

Re-sequencing pathogen microarray

Device and method for digital multiplex PCR assays

Sequence matching algorithm

Family inheritance

Genetic comparisons between grandparents and grandchildren

Identification of related residues in biomolecular sequences by multiple sequence alignment and phylogenetic analysis

System and method for identification of microRNA target sites and corresponding targeting microRNA sequences

Sequence covariance networks, methods and uses therefor

Recombinant meso-active thermostable proteins and processes of design and biosynthesis thereof

Method and apparatus for detecting consensus motifs in data sequences

Methods, systems, and software for identifying functional biomolecules

System for obfuscating identity

Method, system and software arrangement for detecting or determining similarity regions between datasets

Gene finding using ordered sets of distinct marker strings

Method and apparatus for detection, identification and quantification of single-and multi-analytes in affinity-based sensor arrays

Method and system for faster and more sensitive homology searching

Methods, systems, and software for identifying functional biomolecules

Computer method and system for storing and presenting sequence data

Performing sequence analysis as a relational join

Pharmaceutical composition containing a stabilised mRNA optimised for translation in its coding regions

Methods and systems for genomic analysis

Load balancing and conflict processing in workflow with task dependencies

Patient-and condition-specific platelet transfusion support

Distributed data processing platform for metagenomic monitoring and characterization

Metagenomics-based characterization using genomic and epidemiological comparisons

Methods and systems for storing sequence read data

In-database single-nucleotide genetic variant analysis

Method and system for DNA mixture analysis