Showing items 1–100
Simultaneous determination of aneuploidy and fetal fraction
Grant US-11952623-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-11913065-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-11879158-B2
United States of America
Analyzing copy number variation in the detection of cancer
Grant US-11875899-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-11773453-B2
United States of America
Methods and systems for detecting genetic variants
Grant US-11767556-B2
United States of America
Methods and systems for detecting genetic variants
Grant US-11767555-B2
United States of America
Systems and methods for analyzing viral nucleic acids
Grant US-11702708-B2
United States of America
Systems and methods for epigenetic analysis
Grant US-11697835-B2
United States of America
Detecting and classifying copy number variation
Grant US-11697846-B2
United States of America
Fetal aneuploidy detection by sequencing
Grant US-11674176-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-11667959-B2
United States of America
Methods and systems for detecting genetic variants
Grant US-11667967-B2
United States of America
Methods and systems for detecting genetic variants
Grant US-11649491-B2
United States of America
Systems and methods for mitochondrial analysis
Grant US-11649495-B2
United States of America
Methods and systems for detecting genetic variants
Grant US-11639525-B2
United States of America
Methods and systems for detecting genetic variants
Grant US-11639526-B2
United States of America
Methods and compositions for screening and treating developmental disorders
Grant US-11618925-B2
United States of America
Nick-based data storage in native nucleic acids
Grant US-11538554-B1
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-11447813-B2
United States of America
Methods and systems for detecting genetic variants
Grant US-11434531-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-11434523-B2
United States of America
Biological graph or sequence serialization
Grant US-11347704-B2
United States of America
Methods and compositions for screening and treating developmental disorders
Grant US-11339439-B2
United States of America
Method for determining copy number variations
Grant US-11332774-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-11319598-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-11319597-B2
United States of America
Method for determining copy number variations
Grant US-11286520-B2
United States of America
Methods to determine tumor gene copy number by analysis of cell-free DNA
Grant US-11242569-B2
United States of America
Methods and compositions for screening and treating developmental disorders
Grant US-11174516-B2
United States of America
Bambam: parallel comparative analysis of high-throughput sequencing data
Grant US-11164656-B2
United States of America
Bambam: parallel comparative analysis of high-throughput sequencing data
Grant US-11158397-B2
United States of America
Methods and systems for detecting genetic variants
Grant US-11149306-B2
United States of America
Methods and systems for detecting genetic variants
Grant US-11149307-B2
United States of America
BAMBAM: parallel comparative analysis of high-throughput sequencing data
Grant US-11152080-B2
United States of America
Detecting chromosomal aberrations associated with cancer using genomic sequencing
Grant US-11142799-B2
United States of America
BAMBAM: parallel comparative analysis of high-throughput sequencing data
Grant US-11133085-B2
United States of America
Methods and systems for detecting genetic variants
Grant US-11118221-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-11091797-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-11091796-B2
United States of America
WHOLE-GENOME AND TARGETED HAPLOTYPE RECONSTRUCTION
Grant EP-3022320-B1
European Patent Office
Methods and compositions for enriching non-host sequences in host samples
Grant US-11035000-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-11001899-B1
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10995376-B1
United States of America
BamBam: parallel comparative analysis of high-throughput sequencing data
Grant US-10991451-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10982265-B2
United States of America
BamBam: parallel comparative analysis of high-throughput sequencing data
Grant US-10971248-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10961592-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10947600-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10894974-B2
United States of America
Methods and systems for detecting genetic variants
Grant US-10889858-B2
United States of America
Methods and systems for detecting genetic variants
Grant US-10883139-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10876172-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10876152-B2
United States of America
BamBam: parallel comparative analysis of high-throughput sequencing data
Grant US-10878937-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10876171-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10870880-B2
United States of America
NONINVASIVE DIAGNOSIS OF FETAL ANEUPLOIDY BY SEQUENCING
Application EP-3751005-A2
European Patent Office
Systems and methods to detect rare mutations and copy number variation
Grant US-10822663-B2
United States of America
BAMBAM: parallel comparative analysis of high-throughput sequencing data
Grant US-10825552-B2
United States of America
Bambam: parallel comparative analysis of high-throughput sequencing data
Grant US-10825551-B2
United States of America
Methods and systems for detecting genetic variants
Grant US-10801063-B2
United States of America
Systems and methods for epigenetic analysis
Grant US-10793895-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10793916-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10738364-B2
United States of America
BAMBAM: parallel comparative analysis of high-throughput sequencing data
Grant US-10726945-B2
United States of America
Systems and methods for analyzing viral nucleic acids
Grant US-10724110-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10704086-B2
United States of America
Fetal aneuploidy detection by sequencing
Grant US-10704090-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10704085-B2
United States of America
Bambam: parallel comparative analysis of high-throughput sequencing data
Grant US-10706956-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10683556-B2
United States of America
Resolving genome fractions using polymorphism counts
Grant US-10658070-B2
United States of America
Detecting genetic aberrations associated with cancer using genomic sequencing
Grant US-10619214-B2
United States of America
Diagnosis of fetal abnormalities using polymorphisms including short tandem repeats
Grant US-10591391-B2
United States of America
Detecting and classifying copy number variation
Grant US-10586610-B2
United States of America
Systems and methods for mitochondrial analysis
Grant US-10584380-B2
United States of America
Pinhole zero-mode waveguides
Grant US-10570444-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10501810-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10501808-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10494678-B2
United States of America
Analyzing copy number variation in the detection of cancer
Grant US-10482993-B2
United States of America
Systems and methods to detect rare mutations and copy number variation
Grant US-10457995-B2
United States of America
Detecting and classifying copy number variation
Grant US-10415089-B2
United States of America
Analyzing copy number variation in the detection of cancer
Grant US-10388403-B2
United States of America
Portable and low-error DNA-based data storage
Grant US-10370246-B1
United States of America
Compositions and methods for co-amplifying subsequences of a nucleic acid fragment…
Grant US-10364464-B2
United States of America
Using size and number aberrations in plasma DNA for detecting cancer
Grant US-10364467-B2
United States of America
Method and system for network modeling to enlarge the search space of candidate genes for…
Grant US-10347359-B2
United States of America
BAMBAM: parallel comparative analysis of high-throughput sequencing data
Grant US-10268800-B2
United States of America
Bambam: parallel comparative analysis of high-throughput sequencing data
Application US-10249384-B2
United States of America
BAMBAM: parallel comparative analysis of high-throughput sequencing data
Application US-10242155-B2
United States of America
Systems and methods for transcriptome analysis
Application US-10204207-B2
United States of America
Systems and methods for interpreting a human genome using a synthetic reference sequence
Grant US-10127346-B2
United States of America
NONINVASIVE DIAGNOSIS OF FETAL ANEUPLOIDY BY SEQUENCING
Application EP-3378951-A1
European Patent Office
Systems and methods for using paired-end data in directed acyclic structure
Application US-10055539-B2
United States of America
Method and system for the use of biomarkers for regulatory dysfunction in disease
Grant US-9946835-B2
United States of America
Clinical use of an Alu element based bioinformatics methodology for the detection and…
Application US-9932640-B1
United States of America
Methods and systems for aligning sequences
Grant US-9898575-B2
United States of America
Showing items 1–100