Late Quaternary loss of genetic diversity in muskox (Ovibos)
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* Corresponding author: Ross DE MacPhee macphee@amnh.org
- Equal contributors
1 Division of Vertebrate Zoology, American Museum of Natural History, New York, New York 10024, USA
2 Laboratory of Mammals, Zoological Institute, Russian Academy of Sciences, Universitetskaya nab. 1, 199034, St. Petersburg, Russia
3 Cerpolex/Mammuthus, Gudumholm 41, NL-2133 HG Hoofddorp, Netherlands
4 GSF-National Research Center for Environment and Health, Institute of Molecular Virology, Ingolstaedter Landstr.1, 85764 Neuherberg, Germany
BMC Evolutionary Biology 2005, 5:49 doi:10.1186/1471-2148-5-49
Published: 6 October 2005Additional files
Additional File 1:
Alignment of hypervariable region clones from overlapping PCR fragments used to determine the sequences for each specimen analyzed. The consensus sequence of OMModCl was used as a reference. Dots indicate identity to the consensus sequence. Differences are indicated. Base pair sequences that could not be determined for a given clone are marked "N". Gaps are indicated by "-". The first clone provides the name of each sample according to the labels provided in table 1. The numbers indicate PCR replication + clone number: thus 1.1 indicates PCR 1, first clone sequence.
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Additional File 2:
Alignment of cyt bclones from overlapping PCR fragments used to determine the sequences for each specimen analyzed. Symbols as in additional fig. 1.
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Additional File 3:
Alignment of clones from overlapping PCR fragments used to determine 1,180 bp of OMTai39 cyt b. Symbols as in additional fig. 1. The reference is a modern muskox sequence taken from GenBank. Four additional modern muskox sequences are included in the alignment.
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Additional File 4:
Clone sequences derived from multiple amplifications of sample OMBolL15564. All symbols are the same as in additional fig. 1, 2, 3. The modern DNA consensus sequence from additional fig. 1 is used as a reference sequence.
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