Information on SNPs identified from transcriptome data (vcf file)
收藏DataONE2014-07-01 更新2024-06-27 收录
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SNPs identified from transcriptome alignment files in variant call format. SNPs were identified using GATK. Parameters and filters for calling SNPs are listed in header. Additional hard filters include removal of SNPs where every individual was heterozygous, overall SNP depth > 10, overall SNP depth < 350, and minor allele frequency (MAF) > 0.025.
创建时间：
2014-07-01
