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Schmitt et al. BMC Genomics 2010, 11:80 http://www.biomedcentral.com/1471-2164/11/80 METHODOLOGY ARTICLE Open Access Tracking chromosomal positions of isomers a case study with Illumine's BovineSNP50
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To fill out tracking chromosomal positions, follow these steps:

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Gather the necessary data: You will need access to genomic sequence information and genetic markers that can be used to identify specific chromosomal positions.
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Prepare the samples: Depending on the mapping technique chosen, you may need to extract and purify genomic DNA, prepare chromosome spreads, or label specific DNA probes. Follow the recommended protocols for sample preparation.
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Tracking chromosomal positions is the process of identifying and monitoring the specific locations of chromosomes within an organism's genome.
The requirement to file tracking chromosomal positions generally depends on the specific regulations or guidelines set by the governing body or institution overseeing genetic research or genomic studies.
The process of filling out tracking chromosomal positions typically involves collecting and organizing data on the positions of chromosomes, using standardized formats or tools provided by the respective scientific community or regulatory authorities.
The purpose of tracking chromosomal positions is to gain a better understanding of the structure and organization of an organism's genome, which can contribute to various areas of genetic research, such as identifying genetic variants, mapping genes, or studying chromosomal abnormalities.
The specific information that must be reported on tracking chromosomal positions may vary depending on the goals and requirements of the study or the regulations in place. Generally, it would include the chromosome number, position coordinates, and potentially additional annotations or related data.
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