utils | R Documentation |
val_ag_name() validation of name of binding locus
val_ag_name(ag_present) preproc(allele_in, link) pull_seq(alleles_in, tbl_ref_in) comb_pred_tbl(nm_method, nm_sht, nm_fd, thold_score, thold_rank) comb_pred_tbl_mhcI(nm_method, nm_fd, thold_score, thold_rank) find_nonself(dat_in) pull_ag_self(vec_in) find_core_mut(dat_in) align_seq(seq1, seq2, gapopening = 0, gapextension = 8) pull_obj_name(x)
ag_present |
a vector of locus name(s) to make binding predictions for preproc() format and validate allele names |
allele_in |
a vector contains allele name(s) |
link |
a string of url of MHC I or II api pull_seq() pull out sequence of each allele based on ref table |
alleles_in |
vector, allele names |
tbl_ref_in |
dataframe, reference table, default is human_all.csv from github comb_pred_tbl() combine individual prediction tables by method, exclude none-binders and keep strong and weak binders only |
nm_method |
string, prediction method used for IEDB prediction |
nm_sht |
string, short name of alleles |
nm_fd |
string, folder name which contains predict tables from IEDB |
thold_score |
list of vectors, binder thresholds by ic50 score |
thold_rank |
vector, binder thresholds by percentile rank find_nonself() find nonself binding peptides |
dat_in |
dataframe with pep_stim, core, pep_self selected from pull_ag_self align_seq() align protein sequences |
vec_in |
dataframe with pep_stim, core, aligned ag_stim and ag_self columns find_core_mut() find mutation position to core |
seq1 |
string, unaligned sequence of ag_stim |
seq2 |
string, unaligned sequence of ag_self |
gapopening |
numeric, the cost for opening a gap in the alignment. |
gapextension |
numeric, the incremental cost incurred along the length of the gap in the alignment pull_obj_name() |
x, |
name of an object |
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