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PySmooth: a Python tool for the removal and correction of genotyping errors.

BMC research notes - 11 Apr 2024

Soibam Benjamin, Roman Gregg

Abstract excerpt

In genetic mapping studies involving many individuals, genome-wide markers such as single nucleotide polymorphisms (SNPs) can be detected using different methods. However, it comes with some errors. Some SNPs associated with diseases can be in regions encoding long noncoding RNAs (lncRNAs). Therefore, identifying the errors in genotype file and correcting them is crucial for accurate genetic mapping studies. We...

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PMID: 38605369
DOI: 10.1186/s13104-024-06753-4
PMCID: PMC11010338

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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