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Article

PennCNV in whole-genome sequencing data.

BMC bioinformatics - 3 Oct 2017

de Araújo Lima Leandro, Wang Kai

Abstract excerpt

BACKGROUND: The use of high-throughput sequencing data has improved the results of genomic analysis due to the resolution of mapping algorithms. Although several tools for copy-number variation calling in whole genome sequencing have been published, the noisy nature of sequencing data is still a limitation for accuracy and concordance among such tools. To assess the performance of PennCNV original algorithm for...

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Share to Databases, Nucleic Acid
Share to DNA Copy Number Variations
Share to Gene Duplication

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome, Human

Share to Loss of Heterozygosity

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Identifiers

PMID: 28984186
DOI: 10.1186/s12859-017-1802-x
PMCID: PMC5629549

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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