Publications
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Northstar
Northstar
Clinical Validation of Northstar Response, a novel methylated ctDNA therapy response monitoring assay in patients with advanced GI cancer undergoing active treatment
Northstar
Northstar
Clinical Validation of Northstar Response, a novel methylated ctDNA therapy response monitoring assay in patients with advanced GI cancer undergoing active treatment
Unity
Unity
Performance of single-gene noninvasive prenatal testing for autosomal recessive conditions in a general population setting
Unity
Unity
Performance of single-gene noninvasive prenatal testing for autosomal recessive conditions in a general population setting
Unity
Unity
Validation of a Non-invasive Prenatal Test for Fetal RhD, C, c, E, Kell and FyA Antigens
Unity
Unity
Validation of a Non-invasive Prenatal Test for Fetal RhD, C, c, E, Kell and FyA Antigens
Northstar
Northstar
Methylated ctDNA as a biomarker for detecting previously undetectable clinically significant somatic mutations.
Northstar
Northstar
Methylated ctDNA as a biomarker for detecting previously undetectable clinically significant somatic mutations.
Northstar
Northstar
Methylated ctDNA dynamics correspond with clinical tumor load in metastatic lung cancer patients on therapy
Northstar
Northstar
Methylated ctDNA dynamics correspond with clinical tumor load in metastatic lung cancer patients on therapy
Unity
Unity
Maternal carrier screening with single-gene NIPS provides accurate fetal risk assessments for recessive conditions
Unity
Unity
Maternal carrier screening with single-gene NIPS provides accurate fetal risk assessments for recessive conditions
Unity
Unity
Validation of single-gene noninvasive prenatal testing for sickle cell disease
Unity
Unity
Validation of single-gene noninvasive prenatal testing for sickle cell disease
Unity
Unity
Reflex single-gene non-invasive prenatal testing is associated with markedly better detection of fetuses affected with single-gene recessive disorders at lower cost
Unity
Unity
Reflex single-gene non-invasive prenatal testing is associated with markedly better detection of fetuses affected with single-gene recessive disorders at lower cost