Data

SNP annotations for variants associated with calf health traits in Holstein and Jersey dairy cattle

La Trobe University
Amanda Chamberlain (Aggregated by) Iona MacLeod (Aggregated by) Irene Van den Berg (Aggregated by) Jennie Pryce (Aggregated by) M. Michelle Axford (Aggregated by)
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ctx_ver=Z39.88-2004&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Adc&rfr_id=info%3Asid%2FANDS&rft_id=info:doi10.26181/30109231.v1&rft.title=SNP annotations for variants associated with calf health traits in Holstein and Jersey dairy cattle&rft.identifier=10.26181/30109231.v1&rft.publisher=La Trobe University&rft.description=Table S1. Information about the SNPs in high Linkage Disequilibrium (LD) with each lead SNP for Stillbirth in Holstein, Stillbirth in Jersey and Pre-weaning mortality in Holstein cattle.Table S2. Information about the SNPs bound within the start and end position of Haplotypes for Stillbirth in Holstein, Stillbirth in Jersey and Pre-weaning mortality in Holstein cattle. Variants with a minor allele frequency >=0.05 and of moderate or severe consequence are included.&rft.creator=Amanda Chamberlain&rft.creator=Iona MacLeod&rft.creator=Irene Van den Berg&rft.creator=Jennie Pryce&rft.creator=M. Michelle Axford&rft.creator=Majid Khansefid&rft.creator=Mekonnen Haile-Mariam&rft.creator=Michael Goddard&rft.creator=Tuan V. Nguyen&rft.date=2025&rft_rights= https://creativecommons.org/licenses/by/4.0/&rft_subject=Agricultural, veterinary and food sciences&rft_subject=calf health&rft_subject=stillbirth&rft_subject=whole-genome sequence data&rft_subject=GWAS&rft_subject=haplotypes&rft.type=dataset&rft.language=English Access the data

Full description

Table S1. Information about the SNPs in high Linkage Disequilibrium (LD) with each lead SNP for Stillbirth in Holstein, Stillbirth in Jersey and Pre-weaning mortality in Holstein cattle.

Table S2. Information about the SNPs bound within the start and end position of Haplotypes for Stillbirth in Holstein, Stillbirth in Jersey and Pre-weaning mortality in Holstein cattle. Variants with a minor allele frequency >=0.05 and of moderate or severe consequence are included.

Issued: 17 09 2025

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Identifiers
ACN 633 798 857