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The NGS data (VCF files) contain the variants from all the transcripts for a particular gene. Which is the best site/tool to filter out all the non-primary transcripts.
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I tried designing primers for ELANE gene and came up with the following two sequences in in-silico PCR: >chr19:855442+856209 768 bp size >chr19_KI270868v1_alt:34328+35095 768 bp size. Both...
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