Anwa HereditaryScope®
استعرض التفاصيل الكاملة لهذا الفحص التشخيصيمعلومات الفحص
الاسم: Anwa HereditaryScope®
الكود: G5627-AN
نوع العينة: Peripheral Blood
المدة المتوقعة (TAT): 16 يوم
التحضيرات والملاحظات
10ml Peripheral Blood An innovative NGS panel that includes a meticulously curated collection of 146 genes well-established in their associations with hereditary cancer including breast, prostate, Lynch syndrome and Wilms tumor. - Confidently call all variants including MSH2 c.942+3A>T variant a wide range of CNVs in genes Signature : SNVs,Indels,CNVs
فحوصات مقترحة أخرى
- Oligoclonal Bands, CSF/Serum
- SEND OUT TEST PRE-NATAL GENE PANEL (501-1000 GENES) FULL ANALYSIS (EXONS AND INTRONS) SEQUENCING AND CNV + MCC GERMLINE WITH REPORTING AMNIOTIC FLUID CVS BLOOD NGS
- RNA Single gene Fusion analysis by NGS , Tissue for solid tumor
- Coccidioides Antibody, Immunodiffusion, Alias Name is Valley Fever
- RNP Antibodies, IgG, Serum