\HeaderA{hsahomologyLL2HGID}{Mappings between public database ids and NCBI's Internal
HomoloGeneIDs for Homo sapiens}{hsahomologyLL2HGID}
\aliasA{hsahomologyACC2HGID}{hsahomologyLL2HGID}{hsahomologyACC2HGID}
\aliasA{hsahomologyHGID2ACC}{hsahomologyLL2HGID}{hsahomologyHGID2ACC}
\aliasA{hsahomologyHGID2LL}{hsahomologyLL2HGID}{hsahomologyHGID2LL}
\keyword{datasets}{hsahomologyLL2HGID}
\begin{Description}\relax
R environments that provides mappings between public database ids and internal
HomoloGeneIDs (HGID) used by NCBI to represent sequences for
Homo sapiens. Public database ids include LocusLink ids (LL) and GenBank
Accesion/RefSeq numbers (ACC).
\end{Description}
\begin{Details}\relax
Each R environment provides mapping between either HomoloGeneIds and
database ids, or the converse. The mapping direction is indicated by
the name of the environment. For instance, hsahomologyACC2HGID provides
mappings between GenBank accession numbers and HomoloGeneIds.

For each environment, a given id will map to a named vector of ids,
the names of which are the NCBI code for that organism.

Mappings contained were based on data provided by HomoloGene.

HomoloGene:\url{ ftp://ftp.ncbi.nih.gov/pub/HomoloGene/old/hmlg.ftp}. Built: HomoloGene built date not available

Packagebuilt Sun May 15 12:34:37 2005
\end{Details}
\begin{References}\relax
\url{http://www.ncbi.nih.gov/entrez/query.fcgi?db=homologene}
\end{References}
\begin{Examples}
\begin{ExampleCode}
    require("annotate") || stop("annotate unavailable")
    xx <- as.list(hsahomologyLL2HGID)
        if(length(xx) > 5){
                # Get the value of the first key
                xx[2]
                # Get the value for a few keys
                if(length(xx) >= 3){
                        xx[2:4]
                }
        }
\end{ExampleCode}
\end{Examples}

