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Additional file 1 of Genome-wide detection of copy number variation in American mink using whole-genome sequencing

Year: 2022

Type: dataset

Abstract: Additional file 1: Table S1. List of CNVs identified on 100 American mink genomes. Table S2. Detail information of the detected CNVR. Table S3. List of genes completely/partially overlapped with CNVR in American mink. Table S4. Functional enrichment of gene ontology analysis of genes covered by CNVR. Table S5. Functional enrichment of KEGG pathway analysis of genes covered by CNVR.

Source: Figshare

DOI: 10.6084/m9.figshare.21087578

Authors: Davoudi, Pourya, Do, Duy Ngoc, Rathgeber, Bruce, Colombo, Stefanie M., Sargolzaei, Mehdi, Plastow, Graham, Wang, Zhiquan, Karimi, Karim, Hu, Guoyu, Valipour, Shafagh, Miar, Younes

Institutions: Dalhousie University, University of Guelph, University of Alberta

Language: English

Topic: Genomic variations and chromosomal abnormalities

Subfield: Genetics

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

Open Access status: green

OpenAlex ID: W4394520744

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