|
US2019267110A1
|
|
System and method for sequence identification in reassembly variant calling
|
|
US2019214110A1
|
|
Detection of insufficient homology regions in a reference sequence
|
|
US2019129769A1
|
|
System and method for dynamic control of workflow execution
|
|
US2018253553A1
|
|
Data security in bioinformatic sequence analysis
|
|
US2018253536A1
|
|
Watermarking for data security in bioinformatic sequence analysis
|
|
US2018247016A1
|
|
Systems and methods for providing assisted local alignment
|
|
US2018157792A1
|
|
Systems and methods for aligning sequences to personalized references
|
|
US2018081717A1
|
|
Hashing data-processing steps in workflow environments
|
|
US2018039730A1
|
|
Computer Method and System of Identifying Genomic Mutations Using Graph-Based Local Assembly
|
|
US2018089369A1
|
|
Systems and methods for sequence encoding, storage, and compression
|
|
US2017318119A1
|
|
Methods and systems for stream-processing of biomedical data
|
|
US2018053328A1
|
|
Systems and methods for processing computational workflows
|
|
US2017206242A1
|
|
Methods and systems for generating, by a visual query builder, a query of a genomic data store
|
|
US2018173848A1
|
|
Generation and use of simulated genomic data
|
|
US2018137387A1
|
|
Systems and methods for aligning sequences to graph references
|
|
US2018060480A1
|
|
Systems and methods for detecting recombination
|
|
US2018018423A1
|
|
Systems and methods for reconciling variants in sequence data relative to reference sequence data
|
|
US2018004891A1
|
|
Method and apparatus for identifying tandem repeats in a nucleotide sequence
|
|
WO2016141294A1
|
|
Systems and methods for genomic pattern analysis
|
|
US2017242958A1
|
|
Systems and methods for genotyping with graph reference
|
