Showing results 1 to 4 of 4
Title | Author(s) | Issue Date | |
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A new machine-learning based method to accurately assess copy number variants from whole genome sequencing data and its application on the analysis of the Hirschsprung disease genome Proceeding/Conference:American Society of Human Genetics (ASHG) 2019 Annual Meeting | 2019 | ||
A random forest-based framework for genotyping and accuracy assessment of copy number variations Journal:NAR Genomics and Bioinformatics | 2020 | ||
2013 | |||
Third-generation genome sequencing implicates medium-sized structural variants in chronic schizophrenia Journal:Frontiers in Neuroscience | 11-Jan-2023 |