The characterization of multigene families with high copy number variation is often approached through PCR amplification with highly degenerate primers to account for all expected variants flanking th
Designation of PNLIPRP2 variants with respect to the NCBI reference sequence corresponding to the minor truncation allele and the full-length major allele used as the reference in this study.
Resolved alleles for Anas crecca crecca (n = 50)and Anas crecca carolinensis (n = 50) for intron 13 of the GRIN1 gene. This file is formatted for analyses in Arlequin, and sequences are sorted between
