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RexPrimer :explode: (Features :check: (Various database can be used to…
RexPrimer :explode:
Features :check:
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Gene and non-gene target regions in human genome are included in the primer design for PCR/resequencing and SNP genotyping
Crosschecking target sequence against locally Psedogene.org is adsressed in order to avoid the possible mis-priming.
Users can report the structural polymorphisms by checking target sequence with genomic variation database available
Provide the primer redesign module in which the users can redesign their desired primer based on target location and condition
In-Silico PCR@BIOTEC features is provided for the user to test their resulting primer sequences
Specificity of input primer sequence can be verified by the users from the oligonucleotide checking module.
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Advantages :red_flag:
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Provide variety of database such as human SNP databases, insertion/deletion polymorphisms database, pseudogene database, and structural genomic variation databasesfor the users to check their validity of primer sequence
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User friendly which they provide the useful user guide for the first timer user which can be easily followed
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