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C: Get variant position knowing the gene name, base change, and NM#
5.9 years ago by
bisansamara
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C: Understanding the Notation of Genomic Variation Data
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C: Identify the nearest common SNP to a given rare variant
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C: Read genomic ranges from a very big file in R
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C: Read genomic ranges from a very big file in R
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C: Read genomic ranges from a very big file in R
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C: Read genomic ranges from a very big file in R
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C: Read genomic ranges from a very big file in R
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C: Read genomic ranges from a very big file in R
6.4 years ago by
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