![]() ![]() glabrata, will inform the design of experiments to understand gene function in this unique in vitro snail cell model. The availability of the Bge3 genome sequence, and an awareness of genomic differences with B. glabrata BB02 reference genome in both sequence and structure, and these are likely to have significant biological effects. We also resolved representative karyotypes for the Bge3 subculture, which revealed a mixed population exhibiting substantial aneuploidy, in line with previous reports from other Bge subcultures. Furthermore, we have highlighted and validated high-impact SNVs in genes that have often been studied using Bge cells as an in vitro model, and other genes that may have contributed to the immortalization of this cell line. ![]() Single nucleotide variants (SNVs) were predicted and focus was given to those SNVs that are most likely to affect the structure or expression of protein-coding genes. Here, we report the genome sequence of our laboratory subculture of the Bge cell line (designated Bge3), which we mapped to the B. glabrata BB02 genome sequence was recently released, but nothing is known of the sequence variation between this reference and the Bge cell genome, which has likely accumulated substantial genetic variation in the ~50 years since its isolation. glabrata embryonic (Bge) cell line has been an invaluable resource in these studies. ![]() Much is known regarding the host-parasite interactions of these two organisms, and the B. The aquatic pulmonate snail Biomphalaria glabrata is a significant vector and laboratory host for the parasitic flatworm Schistosoma mansoni, an etiological agent for the neglected tropical disease schistosomiasis. ![]()
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