hgug4110bOMIM          package:hgug4110b.db          R Documentation

_M_a_p _b_e_t_w_e_e_n _M_a_n_u_f_a_c_t_u_r_e_r _I_d_e_n_t_i_f_i_e_r_s _a_n_d _M_e_n_d_e_l_i_a_n _I_n_h_e_r_i_t_a_n_c_e _i_n
_M_a_n (_M_I_M) _i_d_e_n_t_i_f_i_e_r_s

_D_e_s_c_r_i_p_t_i_o_n:

     hgug4110bOMIM is an R object that provides mappings between
     manufacturer identifiers and OMIM identifiers.

_D_e_t_a_i_l_s:

     Each manufacturer identifier is mapped to a vector of OMIM
     identifiers. The vector length may be one or longer, depending on
     how many OMIM identifiers the manufacturer identifier maps to. An
     'NA' is reported for any manufacturer identifier that cannot be
     mapped to an OMIM identifier at this time.

     OMIM is based upon the book Mendelian Inheritance in Man (V. A.
     McKusick) and focuses primarily on inherited or heritable genetic
     diseases. It contains textual information, pictures, and reference
     information that can be searched using various terms, among which
     the MIM number is one. 

     Mappings were based on data provided by: Entrez Gene (
     ftp://ftp.ncbi.nlm.nih.gov/gene/DATA ) on 2008-Apr2

_R_e_f_e_r_e_n_c_e_s:

     <URL: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=gene> <URL:
     http://www3.ncbi.nlm.nih.gov/entrez/query.fcgi?db=OMIM>

_E_x_a_m_p_l_e_s:

             x <- hgug4110bOMIM
             # Get the probe identifiers that are mapped to a OMIM ID
             mapped_probes <- mappedkeys(x)
             # Convert to a list
             xx <- as.list(x[mapped_probes])
             if(length(xx) > 0) {
               # Get the OMIM for the first five probes
               xx[1:5]
               # Get the first one
               xx[[1]]
             }

