190942 ⎘
Identifying ancestral relationships using a continuous stream of input
#902Systems and methods for comprehensive analysis of molecular profiles across multiple tumor and germline exomes
#903Methods for non-invasive prenatal ploidy calling
#904Methods and systems for genomic analysis
#905SYSTEMS AND METHODS FOR DETECTING STRUCTURAL VARIANTS
#906BIOINFORMATICS TOOLS, SYSTEMS AND METHODS FOR SEQUENCE ASSEMBLY
#907Detecting fetal sub-chromosomal aneuploidies
#908Methylation pattern analysis of tissues in a DNA mixture
#909Methods and systems for genetic analysis
#910Non-invasive prenatal diagnosis of fetal genetic condition using cellular DNA and cell free DNA
#911Determination device, computer readable medium, and marker for obtaining information on lung cancer
#912Genetic addiction risk analysis for RDS severity index
#913SYSTEMS AND METHODS FOR IDENTIFYING SIGNIFICANTLY MUTATED GENES
#914Spatial arithmetic method of sequence alignment
#915Deconstructing overlapped peaks in droplet digital polymerase chain reaction data
#916METHODS AND COMPOSITIONS RELATED TO REGULATION OF NUCLEIC ACIDS
#917IMMUNOCOMPETENCE ASSESSMENT BY ADAPTIVE IMMUNE RECEPTOR DIVERSITY AND CLONALITY CHARACTERIZATION
#918Risk calculation for evaluation of fetal aneuploidy
#919AUTOMATED ANALYSIS OF MULTIPLEXED PROBE-TARGET INTERACTION PATTERNS: PATTERN MATCHING AND ALLELE IDENTIFICATION
#920SELECTION DEVICE FOR CANDIDATE SEQUENCE INFORMATION FOR SIMILARITY DETERMINATION, SELECTION METHOD, AND USE FOR SUCH DEVICE AND METHOD
#921Processes and systems for nucleic acid sequence assembly
#922SOFTWARE HAPLOTYING OF HLA LOCI
#923Methods for accurate sequence data and modified base position determination
#924Methods and systems for interpretation and reporting of sequence-based genetic tests
#925Processing and analysis of complex nucleic acid sequence data
#926Biomarkers and methods for predicting benefit of adjuvant chemotherapy
#927ANALYSIS OF NUCLEIC ACID SEQUENCES
#928Systems and methods for interpreting a human genome using a synthetic reference sequence
#929Phased whole genome genetic risk in a family quartet
#930Identification of surface-associated antigens for tumor diagnosis and therapy
#931Systems and methods to detect rare mutations and copy number variation
#932COMPOSITIONS, METHODS AND USES FOR MULTIPLEX PROTEIN SEQUENCE ACTIVITY RELATIONSHIP MAPPING
#933Methods for genome assembly and haplotype phasing
#934Data analysis device and method therefor
#935MOLECULAR PROFILING OF TUMORS
#936Method for development of a peptide building block useful for de novo protein design
#937Systems and methods for plant stress mitigation
#938SYSTEMS AND METHODS FOR IDENTIFYING POLYMORPHISMS
#939Image analysis for breast cancer prognosis
#940Methods and systems for detecting sequence variants
#941Method and system for designing polynucleotide sequences and polynucleotide sequences obtained thereby
#942CHROMOSOME REPRESENTATION DETERMINATIONS
#943Noise reduction methods for nucleic acid and macromolecule sequencing
#944Prefix burrows-wheeler transformations for creating and searching a merged lexeme set
#945Methods for screening, predicting and monitoring prostate cancer
#946Method and System for Matching Probabilistic Identitypes on a Database
#947Dynamic genome reference generation for improved NGS accuracy and reproducibility
#948METHODS AND COMPOSITIONS FOR IDENTIFYING GLOBAL MICROSATELLITE INSTABILITY AND FOR CHARACTERIZING INFORMATIVE MICROSATELLITE LOCI
#949Constructing custom knowledgebases and sequence datasets with publications
#950Systems and methods for validation of sequencing results
#951Rare variant calls in ultra-deep sequencing
#952Recombinant meso-active thermo-stable protein and processes of design and biosynthesis thereof
#953Identification of a person having risk for developing type 2 diabetes
#954USING DOUBLET INFORMATION IN GENOME MAPPING AND ASSEMBLY
#955Mantle phenotype detection in palm
#956Gene fusions and gene variants associated with cancer
#957Methods and kits for monitoring response to radiation therapies in cancer
#958Systems and methods for using paired-end data in directed acyclic structure
#959METHOD AND SYSTEM FOR PROCESSING DATA FOR EVALUATING A QUALITY LEVEL OF A DATASET
#960EFFICIENT COMPARISON OF POLYNUCLEOTIDE SEQUENCES
#961Intermittent detection during analytical reactions
#962Systems and methods for transcriptome analysis
#963HIERARCHICAL GENOME ASSEMBLY METHOD USING SINGLE LONG INSERT LIBRARY
#964Gene fusions and alternatively spliced junctions associated with breast cancer
#965Systems and methods to detect rare mutations and copy number variation
#966Identification of a Person having Risk for Atherosclerosis and Associated Disease by the Person's Gut Microbiome and the Prevention of such Diseases
#967Database-Driven Primary Analysis of Raw Sequencing Data
#968Biomarkers for diabetes and usages thereof
#969Measurement and comparison of immune diversity by high-throughput sequencing
#970Methods for standardized sequencing of nucleic acids and uses thereof
#971String graph assembly for polyploid genomes
#972METHOD AND ARRANGEMENT FOR DETERMINING TRAITS OF A MAMMAL
#973MATERIALS AND METHODS FOR DETERMINING SUSCEPTIBILITY OR PREDISPOSITION TO CANCER
#974Method to Identify Genes Relating to Improved Pathogen Resistance in Plants
#975ANALYZING PROPERTY OF PROTEIN SEQUENCE
#976METHOD FOR QUICK-SEARCH OF LOCI-OF-INTEREST IN A GENE SEQUENCE OF A TARGET BIOLOGICAL VIRUS
#977GENETIC PREDICTORS OF RESPONSE TO TREATMENT WITH CRHR1 ANTAGONISTS
#978Systems and methods for RNA analysis in functional confirmation of cancer mutations
#979Device for detecting a dynamical network biomarker, method for detecting same, and program for detecting same
#980METHODS OF PROGNOSTICATING AND TREATING CANCER
#981ASSAY FOR ANALYSES OF RABIES VIRUS GLYCOPROTEIN
#982Methods of storing information using nucleic acids
#983Encoding and decoding of RNA data
#984METHOD OF DETECTING CHROMOSOMAL ABNORMALITIES
#985APPARATUS AND METHODS FOR ANALYSING BIOCHEMICAL DATA
#986Method and System for Identifying Clinical Phenotypes in Whole Genome DNA Sequence Data
#987Systems and methods for tumor clonality analysis
#988Methods for producing high-fidelity autologous idiotype vaccines
#989Electronic methods and systems for microorganism characterization
#990METHOD OF DETERMINING CLONOTYPES AND CLONOTYPE PROFILES
#991PROGRAMMABLE ITERATED ELONGATION: A METHOD FOR MANUFACTURING SYNTHETIC GENES AND COMBINATORIAL DNA AND PROTEIN LIBRARIES
#992Optical processing
#993Cell-free DNA as a therapeutic target for female infertility and diagnostic marker
#994METHOD FOR OBTAINING AND DETECTING A MARKER OF OBJECTS TO BE IDENTIFIED, RELATED MARKER, AUTHENTICATION METHOD AND VERIFICATION METHOD
#995System and Method for Determining Relatedness
#996Strategies for high throughput identification and detection of polymorphisms
#997MOLECULAR PROFILING OF TUMORS
#998Bioinformatics systems, apparatuses, and methods executed on an integrated circuit processing platform
#999SYSTEM AND METHOD FOR USING GENETIC DATA TO DETERMINE INTRA-TUMOR HETEROGENEITY
#1000Lossless compression of DNA sequences
#1001Systems and methods for analyzing sequence data
#1002METHOD TO REPRESENT THE NUCLEOTIDE ELEMENTS OF A DNA SEQUENCE AS NUMERICAL ELEMENTS TO INCLUDE CYTOSINE BEING ASSIGNED THE VALUE ZERO, THYMINE BEING ASSIGNED THE VALUE ONE, ADENINE BEING ASSIGNED THE VALUE TWO AND GUANINE BEING ASSIGNED THE VALUE THREE
#1003METHOD TO REPRESENT THE NUCLEOTIDE ELEMENTS OF A DNA SEQUENCE AS NUMERICAL ELEMENTS TO INCLUDE CYTOSINE BEING ASSIGNED THE VALUE ONE, THYMINE BEING ASSIGNED THE VALUE TWO, ADENINE BEING ASSIGNED THE VALUE THREE, AND GUANINE BEING ASSIGNED THE VALUE FOUR
#1004METHOD TO REPRESENT THE NUCLEOTIDE ELEMENTS OF DNA AS NUMERICAL ELEMENTS TO INCLUDE ADENINE BEING ASSIGNED THE VALUE ZERO, GUANINE BEING ASSIGNED THE VALUE ONE, CYTOSINE BEING ASSIGNED THE VALUE TWO AND THYMINE BEING ASSIGNED THE VALUE THREE
#1005Method for identifying novel minor histocompatibility antigens
#1006Haplotying of HLA loci with ultra-deep shotgun sequencing
#1007Methods and apparatus for sorting data
#1008BIOMARKER SIGNATURE METHOD, AND APPARATUS AND KITS THEREFOR
#1009Method and system for microbiome analysis
#1010System for genetic surveillance and analysis
#1011Method and system for microbiome analysis
#1012Method and system for microbiome analysis
#1013Haplotype resolved genome sequencing
#1014METHODS FOR THE SURVEY AND GENETIC ANALYSIS OF POPULATIONS
#1015System and Methods for Detecting Genetic Variation
#1016METHOD OF ANALYZING GENOME BY GENOME ANALYZING DEVICE
#1017Systems and methods for use of known alleles in read mapping
#1018Methods and systems for aligning sequences in the presence of repeating elements
#1019Method and system for quantifying sequence alignment
#1020Methods and systems for genotyping genetic samples
#1021SYSTEMS AND METHODS FOR GENOMIC VARIANT ANALYSIS
#1022Sequence-centric scientific information management
#1023RAPID IDENTIFICATION OF INFECTIOUS MICROORGANISMS AT POINT OF CARE
#1024MICROARRAY FOR DETECTION OF MUTATIONS IN beta-GLOBIN GENES AND DETECTION METHOD THEREOF
#1025ITERATIVE CLUSTERING OF SEQUENCE READS FOR ERROR CORRECTION
#1026DETECTING VARIANTS IN SEQUENCING DATA AND BENCHMARKING
#1027Basecaller for DNA sequencing using machine learning
#1028STRING GRAPH ASSEMBLY FOR POLYPLOID GENOMES
#1029METHODS FOR PREDICTING AND DETECTING CANCER RISK
#1030METAGENOMIC ANALYSIS OF SAMPLES
#1031Compositions and methods for nucleic acid sequencing
#1032System and Methods for Genetic Analysis of Mixed Cell Populations
#1033Methods and systems for storing sequence read data
#1034CALCULATION METHOD FOR INTERCHROMOSOMAL TRANSLOCATION POSITION
#1035Reference markers for biological samples
#1036Grouping and transferring omic sequence data for sequence analysis
#1037Automated nucleic acid repeat count calling methods
#1038Cell-free nucleic acids for the analysis of the human microbiome and components thereof
#1039ENZYMATIC METHOD TO ENRICH FOR CAPPED RNA, KITS FOR PERFORMING SAME, AND COMPOSITIONS DERIVED THEREFROM
#1040Method for synthesizing a nuclease with reduced off-site cleavage
#1041METHOD AND DEVICE FOR LABELLING SINGLE NUCLEOTIDE POLYMORPHISM SITES IN GENOME
#1042Method, computer-accessible medium, and systems for generating a genome wide haplotype sequence
#1043SYSTEM AND METHOD FOR ALIGNING GENOME SEQUENCE IN CONSIDERATION OF ACCURACY
#1044TRANSCRIPTOME ASSEMBLY METHOD AND SYSTEM
#1045PREDICTION OF GENE TARGETS OF ENHANCERS
#1046Systems and methods for transcriptome analysis
#1047Systems and methods for using paired-end data in directed acyclic structure
#1048DNA sequencing
#1049DNA sequencing
#1050Epitope focusing by variable effective antigen surface concentration
#1051High resolution allele identification
#1052Multi-targeting short interfering RNAs
#1053CELL ANALYSIS METHOD, CELL ANALYZER AND SAMPLE SCREENING METHOD
#1054Methods and systems for modeling phasing effects in sequencing using termination chemistry
#1055Methods and processes for non-invasive assessment of genetic variations
#1056Digital counting of individual molecules by stochastic attachment of diverse labels
#1057Minimization of surprisal data through application of hierarchy filter pattern
#1058BAMBAM: parallel comparative analysis of high-throughput sequencing data
#1059Phasing and linking processes to identify variations in a genome
#1060METHOD, SYSTEM AND COMPUTER READABLE MEDIUM FOR DETERMINING BASE INFORMATION IN PREDETERMINED AREA OF FETUS GENOME
#1061Systems, methods, and compositions for viral-associated tumors
#1062PEPTIDE IDENTIFICATION AND SEQUENCING BY SINGLE-MOLECULE DETECTION OF PEPTIDES UNDERGOING DEGRADATION
#1063Molecular profiling of tumors
#1064DNA barcodes for multiplexed sequencing
#1065Method and system for DNA mixture analysis
#1066METHOD FOR FINDING VARIANTS FROM TARGETED SEQUENCING PANELS
#1067Computer-based systems and methods for analyzing genomes based on discrete data structures corresponding to genetic variants therein
#1068Nucleic acid sequencing system and method
#1069Methods and systems of four-valued genomic sequencing and macromolecular analysis
#1070Methods and systems for genomic analysis
#1071SYSTEM AND METHOD FOR ALIGNING GENOME SEQUENCE
#1072COLLAPSIBLE MODULAR GENOMIC PIPELINE
#1073Mass spectrometric data analyzing apparatus and analyzing method
#1074NON-INVASIVE PRENATAL TESTING METHOD BASED ON WHOLE-GENOME TENDENCY SCORING
#1075METHODS FOR ASSESSING ADJUSTED CANCER STAGE OR PROGNOSIS OF SUBJECT WITH HEPATOCELLULAR CARCINOMA
#1076DYNAMIC METHODS FOR DIAGNOSIS AND PROGNOSIS OF CANCER
#1077Methods and systems for aligning sequences
#1078METHOD AND SYSTEM FOR DETERMINING COPY NUMBER VARIATION
#1079Methods and systems for detecting sequence variants
#1080Methods and compositions for identifying repeating sequences in nucleic acids
#1081METHODS FOR IDENTIFICATION OF ORGANISMS, ASSIGNING READS TO ORGANISMS, AND IDENTIFICATION OF GENES IN METAGENOMIC SEQUENCES
#1082Methods of analyzing massively parallel sequencing data
#1083Allelotyping methods for massively parallel sequencing
#1084Control nucleic acid sequences for use in sequencing-by-synthesis and methods for designing the same
#1085Computer Assisted Sperm Profile Analysis and Recognition
#1086Drug discovery methods
#1087METHOD FOR DETECTING BALANCED CHROMOSOMAL ABERRATIONS IN A GENOME
#1088Systems and methods for sequencing in emulsion based microfluidics
#1089Method and system for analyzing noise in an electrophysiology study
#1090NON-INVASIVE DETERMINATION OF METHYLOME OF TUMOR FROM PLASMA
#1091Bacterial Metastructure and Methods of Use
#1092Digital counting of individual molecules by stochastic attachment of diverse labels
#1093Methods and processes for non-invasive assessment of genetic variations
#1094Compositions, kits, and methods for the identification, assessment, prevention, and therapy of cancer
#1095Associative memory and data searching system and method
#1096System and method for real time clinical questions presentation and management
#1097SYSTEM AND METHOD FOR ALIGNING GENOME SEQUENCE
#1098SYSTEM AND METHOD FOR ALIGNING GENOME SEQUENCE CONSIDERING MISMATCH
#1099SYSTEM AND METHOD FOR PROCESSING GENOTYPE INFORMATION RELATING TO TREATMENT WITH PAIN MEDICATION
#1100Bioinformatics systems, apparatuses, and methods executed on an integrated circuit processing platform
#1101Bioinformatics systems, apparatuses, and methods executed on an integrated circuit processing platform
#1102METHOD FOR DETERMINING COPY NUMBER VARIATIONS IN SEX CHROMOSOMES
#1103METHODS FOR IDENTIFYING SEQUENCE MOTIFS, AND APPLICATIONS THEREOF
#1104METHOD FOR DETECTING GENETIC VARIATION
#1105Distributed system providing dynamic indexing and visualization of genomic data
#1106Method for analyzing DNA methylation based on MspJI cleavage
#1107ESTROGEN METABOLITE LEVELS AND CYP1B1 POLYMORPHISMS IN LUNG CANCER DIAGNOSIS, PROGNOSIS, AND RISK ASSESSMENT
#1108Systems and methods for SNP analysis and genome sequencing
#1109COMPUTER READABLE MEDIUM FOR ENABLING A COMPUTER TO CARRY OUT PROVISION OF INFORMATION ON HEPATOCELLULAR CARCINOMA AND MARKER AND KIT FOR OBTAINING INFORMATION ON HEPATOCELLULAR CARCINOMA
#1110COMPUTER READABLE MEDIUM FOR ENABLING A COMPUTER TO CARRY OUT PROVISION OF INFORMATION ON COLON CANCER AND MARKER AND KIT FOR OBTAINING INFORMATION ON COLON CANCER
#1111COLLOCATED SYSTEMS FOR STORING, PROCESSING AND UTILIZING GENETIC INFORMATION
#1112MDM2-Containing Double Minute Chromosomes And Methods Therefore
#1113Method and system for genome identification
#1114CLUSTERING COPY-NUMBER VALUES FOR SEGMENTS OF GENOMIC DATA
#1115METHOD, APPARATUS, AND KIT FOR ANALYZING GENES
#1116SYSTEM AND METHOD FOR MANAGING GENOMIC TESTING RESULTS
#1117SYSTEM AND METHOD FOR ALIGNING GENOME SEQUENCE IN CONSIDERATION OF READ QUALITY
#1118METHOD AND SYSTEM FOR DETERMININING WHETHER GENOME IS ABNORMAL
#1119Methods for non-invasive prenatal ploidy calling
#1120Diagnosing fetal chromosomal aneuploidy using massively parallel genomic sequencing
#1121Diagnosing fetal chromosomal aneuploidy using massively parallel genomic sequencing
#1122Providing nucleotide sequence data
#1123Synthetic gene clusters
#1124Methods and apparatus for measuring analytes
#1125METHOD OF DETECTING FUSED TRANSCRIPTS AND SYSTEM THEREOF
#1126METHOD FOR MEASURING SOMATIC DNA MUTATIONAL PROFILES
#1127Methods, Systems, and Computer Readable Media for Improving Base Calling Accuracy
#1128Determining fetal genomes for multiple fetus pregnancies
#1129Bioinformatics systems, apparatuses, and methods executed on an integrated circuit processing platform
#1130METHOD AND SYSTEM FOR PREDICTING A DISEASE
#1131Anti-microbial peptides and methods of use thereof
#1132Methods and processes for calling bases in sequence by incorporation methods
#1133Methods and Compositions for Species-Specific Kinome Microarrays
#1134METHODS AND SYSTEMS TO ANALYZE REACTIONS USING AN INFORMATION SYSTEM
#1135Hardware acceleration of short read mapping for genomic and other types of analyses
#1136IDENTIFICATION AND USE OF CIRCULATING TUMOR MARKERS
#1137Methods, Systems, and Computer Readable Media for Evaluating Variant Likelihood
#1138METHODS FOR EARLY DETECTION OF ESOPHAGEAL CANCER
#1139Device, system and method for securing and comparing genomic data
#1140METHOD FOR SEQUENCE RECOMBINATION AND APPARATUS FOR NGS
#1141CHARACTERIZATION OF BIOLOGICAL MATERIAL IN A SAMPLE OR ISOLATE USING UNASSEMBLED SEQUENCE INFORMATION, PROBABILISTIC METHODS AND TRAIT-SPECIFIC DATABASE CATALOGS
#1142Processes of identifying and characterizing X-linked disorders
#1143DISTANCE MAPS USING MULTIPLE ALIGNMENT CONSENSUS CONSTRUCTION
#1144Conserved Nucleotide Elements In Ribosomal RNA
#1145Computer Files and Methods Supporting Forensic Analysis of Nucleotide Sequence Data
#1146Set membership testers for aligning nucleic acid samples
#1147SEQUENCE ASSEMBLY USING OPTICAL MAPS
#1148METHOD FOR DETECTING MICRO-DELETION AND MICRO-REPETITION OF CHROMOSOME
#1149SEQUENTIAL SEQUENCING
#1150Spatial sequencing/gene expression camera
#1151METHOD AND SYSTEM FOR ANALYZING THE TAXONOMIC COMPOSITION OF A METAGENOME IN A SAMPLE
#1152Systems and Methods for Determining Copy Number Variation
#1153Methods for accurate sequence data and modified base position determination
#1154SYSTEM AND METHOD FOR CLEANING NOISY GENETIC DATA FROM TARGET INDIVIDUALS USING GENETIC DATA FROM GENETICALLY RELATED INDIVIDUALS
#1155Method for Assembly of Nucleic Acid Sequence Data
#1156Method and kit for characterizing microorganisms
#1157Methods, systems, and software for identifying functional bio-molecules
#1158SURPRISAL DATA REDUCTION OF GENETIC DATA FOR TRANSMISSION, STORAGE, AND ANALYSIS
#1159Maternal plasma transcriptome analysis by massively parallel RNA sequencing
#1160BIOINFORMATICS SYSTEMS, APPARATUSES, AND METHODS EXECUTED ON AN INTEGRATED CIRCUIT PROCESSING PLATFORM
#1161Algorithms for sequence determinations
#1162Methods and Compositions for Identifying Global Microsatellite Instability and for Characterizing Informative Microsatellite Loci
#1163GENOMIC/PROTEOMIC SEQUENCE REPRESENTATION, VISUALIZATION, COMPARISON AND REPORTING USING BIOINFORMATICS CHARACTER SET AND MAPPED BIOINFORMATICS FONT
#1164METHOD AND DEVICE FOR OPTIMIZING A NUCELOTIDE SEQUENCE FOR THE PURPOSE OF EXPRESSION IN A PROTEIN
#1165METHOD AND SYSTEM FOR DETERMINING CHROMOSOME ANEUPLOIDY OF SINGLE CELL
#1166Detection of genetic or molecular aberrations associated with cancer
#1167Mass Spectrometry
#1168Molecular profiling of tumors
#1169Methods for genome assembly and haplotype phasing
#1170Methods and systems for nucleic acid sequence analysis
#1171Methods and systems for using a cloud computing environment to configure and sell a biological sample preparation cartridge and share related data
#1172Efficient genomic read alignment in an in-memory database
#1173System for genomic data processing with an in-memory database system and real-time analysis
#1174SYSTEM AND METHOD FOR RECOMBINATION OF GENOME SEQUENCE CONSIDERING READ LENGTH
#1175Strategies for high throughput identification and detection of polymorphisms
#1176TREATMENT AND DIAGNOSIS OF EPIGENETIC DISORDERS AND CONDITIONS
#1177METHOD AND APPARATUS OF ALIGNING A READ SEQUENCE
#1178Systems and methods for identifying Replikin Scaffolds and uses of said Replikin Scaffolds
#1179Haplotying of HLA loci with ultra-deep shotgun sequencing
#1180SINGLE CELL CLASSIFICATION METHOD, GENE SCREENING METHOD AND DEVICE THEREOF
#1181Bioinformatics systems, apparatuses, and methods executed on an integrated circuit processing platform
#1182Method and device for genetic map construction, method and device for haplotype analysis
#1183Partition defined detection methods
#1184Determination of copy number variations using binomial probability calculations
#1185OLIGOMER SEQUENCES MAPPING
#1186Determination of copy number variations using binomial probability calculations
#1187METHODS AND APPARATUS FOR ANALYZING GENETIC INFORMATION
#1188Methods and processes for non-invasive assessment of genetic variations
#1189Parallel local sequence alignment
#1190Stable genes in comparative transcriptomics
#1191Molecular profiling of tumors
#1192METHOD AND APPARATUS FOR PERFORMING DRUG SCREENING
#1193Stable genes in comparative transcriptomics
#1194ANALYZING SHORT TANDEM REPEATS FROM HIGH THROUGHPUT SEQUENCING DATA FOR GENETIC APPLICATIONS
#1195Methods and materials for assessing allelic imbalance
#1196SYSTEMS AND METHODS FOR OBTAINING AND MANAGING SEQUENCE DATA
#1197Analysis of DNA samples
#1198Processing data from genotyping chips
#1199Accurate and fast mapping of reads to genome
#1200High resolution analysis of mammalian transcriptome using gene pool specific primers