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“CNVs identified by NGS based approach accounted for 9.5% (27/287) of pathogenic variants”
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New article: Analysis of Sequence and Copy Number Variants in Canadian Patient Cohort With Familial Cancer Syndromes Using a Unique Next Generation Sequencing Based Approach https://t.co/Sd9Ol22OfR #colorectalcancer #oncology https://t.co/cVwehvJVPA
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New Research: Analysis of Sequence and Copy Number Variants in Canadian Patient Cohort With Familial Cancer Syndromes Using a Unique Next Generation Sequencing Based Approach: Background Hereditary cancer predisposition syndromes account for… https://t.co/