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文献和实验Human Complement Components C4A and C4B Genetic Diversities: Complex Genotypes and Phenotypes
, respectively, in B. (B ) Module‐specific PCR of genomic DNA samples from five human subjects with two, three, four, five, and six C4 gene copies. Left panel, primer set a, b, and c was used. Right panel, primer set b, c, and d was used. The lower panels depict
Using the Ensembl Genome Server to Browse Genomic Sequence Data
Figure 1.15.5 Ensembl Gene Variation image page for the human SMAD2 gene showing transcript models for the three alternative splice variants annotated for this gene. While exon‐intron structures are drawn
PolyPhred Analysis Software for Mutation Detection from Fluorescence‐Based Sequence Data
is required if one wishes to identify 100% of the variants in a sample set. Curr. Protoc. Hum. Genet. 59:7.16.1?7.16.21. © 2008 by John Wiley & Sons, Inc. Keywords: DNA sequencing; mutation identification; SNPs; indels; sequence traces
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