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A Simple Method to Confirm and Size Deletion, Duplication, and Insertion Mutations Detected by Sequence Analysis
Characterizing heterozygous insertions or deletions in genes by PCR and Sanger sequencing can be a challenge due to overlapping sequencing traces produced by overlapping templates. This is particularly problematic for clinical diagnostic laboratories, because mutations must be precisely characterize...
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Päätekijät: | , , , , |
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Aineistotyyppi: | Artigo |
Kieli: | Inglês |
Julkaistu: |
American Society for Investigative Pathology
2010
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Aiheet: | |
Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2928424/ https://ncbi.nlm.nih.gov/pubmed/20639189 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2353/jmoldx.2010.100011 |
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