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Updated: Jan 14, 2026

Detection of Copy Number Alterations Using Single Cell Sequencing
Published on: February 17, 2017
ParaMask: a new method to identify multicopy genomic regions, corrects major biases in whole-genome sequencing data
Bastiaan Tjeng1, Male Arimond1, Helene Bråten Grindeland1
1Max Planck Institute for Plant Breeding Research, Carl-von-Linne-Weg 10, 50829, Cologne, Germany.
Abstract:
Multicopy genomic regions are repeated sequences that can bias genomic analyses. Here, we present a method, ParaMask, to identify and filter multicopy regions in population-level genomic data of any species. The broad applicability of this method stems from a flexible Expectation-Maximization framework to detect excess heterozygosity while simultaneously fitting inbreeding levels. By combining this signature with read-ratio deviations, excess sequencing depth, and a clustering technique, our method attains high recall. We show that multicopy regions create biases that confound evolutionary genomic analyses and that by identifying these regions with our method and filtering them, we can correct these biases.
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Genome Copying Errors
Comparing Copy Number Variations and SNPs
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...

