Variants detected by whole genome re-sequencing of an affected Pezzata Rossa cow.
收藏NIAID Data Ecosystem2026-03-08 收录
数据链接：
官方服务：
资源简介：
a The sequences were compared to the reference genome (UMD3.1 assembly). b The following snpEFF categories of variants were considered as coding: SYNONYMOUS_CODING, NON_SYNONYMOUS_CODING, CODON_DELETION, CODON_INSERTION, CODON_CHANGE_PLUS_CODON_DELETION, CODON_CHANGE_PLUS_CODON_INSERTION, FRAME_SHIFT, EXON_DELETED, START_GAINED, START_LOST, STOP_GAINED, STOP_LOST, SPLICE_SITE_ACCEPTOR, SPLICE_SITE_DONOR. c These variants are listed in S1 Table. d Chr. X g.83,572,401 G>A (ERCC6L) and Chr X g.97,363,937 A>G (TSR2) Variants detected by whole genome re-sequencing of an affected Pezzata Rossa cow.
创建时间：
2015-07-23
