choose_sequence_regions | R Documentation |
This function came out of our TMRC2 work and seeks to provide an initial set of potential PCR primers which are able to distinguish between different aspects of the data. In the actual data, we were looking for differences between the zymodemes 2.2 and 2.3.
choose_sequence_regions(
long_variant_vector,
max_primer_length = 45,
topn = NULL,
bin_width = 600,
genome = NULL,
target_temp = 58,
min_gc_prop = 0.25,
max_nmer_run = 5
)
long_variant_vector |
variant-based set of putative regions with variants between conditions of interest. |
max_primer_length |
given this length as a start, whittle down to a hopefully usable primer size. |
topn |
Choose this number of variant regions from the rather larger set of possibilities.. |
bin_width |
Separate the genome into chunks of this size when hunting for primers, this size will therefore be the approximate PCR amplicon length. |
genome |
(BS)Genome to search. |
target_temp |
PCR temperature to attempt to match. |
min_gc_prop |
Cutoff for minimum required GC content. |
max_nmer_run |
Maximum run of the same nucleotide allowed. |
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