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1. A Robust Approach for Blind Detection of Balanced Chromosomal Rearrangements with Whole‐Genome Low‐Coverage Sequencing. Issue 5 (9th April 2014)

3. Balanced Chromosomal Rearrangement Detection by Low‐Pass Whole‐Genome Sequencing. (24th January 2018)

4. Copy‐Number Variants Detection by Low‐Pass Whole‐Genome Sequencing. (11th July 2017)

6. Development of coupling controlled polymerizations by adapter-ligation in mate-pair sequencing for detection of various genomic variants in one single assay. (7th June 2019)

8. Genome sequencing reveals the role of rare genomic variants in Chinese patients with symptomatic intracranial atherosclerotic disease. Issue 3 (8th December 2021)

9. Identification of balanced chromosomal rearrangements previously unknown among participants in the 1000 Genomes Project: implications for interpretation of structural variation in genomes and the future of clinical cytogenetics. (July 2018)