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Variation
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2018-03-05
相关数据集
SAR11 SAAVs Tables and Figures
Figures, Supplementary Figures, and Supplementary Tables for Delmont and Kiefl et al.
DataCite Commons2020-09-01 更新140
gVCF_NA20850
1000 Genomes gVCF mapped to hs37d5 for NA20850. Complete collection: https://doi.org/10.6084/m9.figshare.c.4414307
DataCite Commons2020-08-27 更新110
gVCF_NA19063
1000 Genomes gVCF mapped to hs37d5 for NA19063. Complete collection: https://doi.org/10.6084/m9.figshare.c.4414307
Figshare2019-04-09 更新30
Additional file 5: of The clinical benefit of array-based comparative genomic hybridization for detection of copy number variants in Czech children with intellectual disability and developmental delay
CNVs of uncertain significance detected by array-CGH in 15 children with ID/DD, ASD and MCA (List 1), cnnLOH detected by CGHâ +â SNP microarrays in 8 children with ID/DD, ASD and MCA (List 2). (XLSX 1
DataCite Commons2020-08-26 更新110
sac.LOH1.snps.unfiltered.vcf
Variant call format of unfiltered SNP data from Saccharomyces cerevisiae clones evolved for 100 days. Supports in prep publication: "High-resolution mapping of loss of heterozygosity in evolved yea
DataCite Commons2020-08-27 更新50
