WO2018026576A1
|
|
Genomic analysis of cord blood
|
WO2017136720A1
|
|
Variant detection of sequencing assays
|
US2017073739A1
|
|
Sample retrieval and genetic analysis thereof
|
CA3035342A1
|
|
Systems and methods for medical genetic testing
|
EP3271481A1
|
|
Methods of quality control using single-nucleotide polymorphisms in pre-implantation genetic screening
|
EP3295183A1
|
|
Devices and systems for barcoding individual wells and vessels
|
EP3271480A1
|
|
Screening for structural variants
|
WO2016061514A1
|
|
Pre-implantation genetic screening and aneuploidy detection
|
CA2999708A1
|
|
Process control for increased robustness of genetic assays
|
WO2016040446A1
|
|
Methods for selectively suppressing non-target sequences
|
US2016048608A1
|
|
Systems and methods for genetic analysis
|
US2015322524A1
|
|
Methods for detecting aneuploidy
|
US2016251719A1
|
|
Methods for copy number determination
|
WO2015057565A1
|
|
Methods for assessing a genomic region of a subject
|
EP3005200A2
|
|
Methods and systems for storing sequence read data
|
WO2014143994A2
|
|
Methods and compositions for evaluating genetic markers
|
US8778609B1
|
|
Methods for analyzing nucleic acids
|
EP2917368A1
|
|
Methods and systems for identifying contamination in samples
|
US2015111203A1
|
|
Methods for determining carrier status
|
US2014129201A1
|
|
Validation of genetic tests
|