These extraction methods describe two protocols for harvesting DNA from rabbit fat, as an example of mammalian fat. It is recommended to use the QIAGEN Genomic-tip 100/G, either following the standard protocol or by performing the tissue lysis with ATL buffer. We found that the use of ATL buffer produced a sample which generated a slightly improved read N50 value, compared with the sample extracted using the standard protocol. We recommend the use of SPRI size selection prior to sequencing. The sequencing performance was assessed using the Ligation Sequencing Kit. To obtain more sequencing data from this sample, users may find that their experiments would benefit from a flow cell wash step.