Systran is what Alta Vista uses to do their translations at the babelfish
site.

FWIW: you might want to just go ahead and use the babelfish or google sites
if these translations are not going to be posted to a site as web pages and
whatnot. The company I work for is French owned and I have a lot of
collegues that will discuss a problem to death in French and then send me a
request to change something in one line of english. most of the time the
discussions are included in the e-mail but as I don't speak French (yet --
I'm starting to pick it up, though, mwahahahahahahaaaa) I have to translate
them to get the gist (jist?) The babelfish site seems to do okay with French
to English

I have other stories about translation (web site content,etc) regarding a
specific vendor if you're interest in who *not* to go with...

will


----- Original Message -----
From: "Dana Tierney" <[EMAIL PROTECTED]>
To: "CF-Community" <[EMAIL PROTECTED]>
Sent: Saturday, May 31, 2003 7:44 AM
Subject: Re: automated translation, argh....


> just to beat this dead horse a little further -- I just did a search in
the
> HoF archives for any discussions on this before I joined these lists, and
> the one additional mention, http://www.systranbox.com/systran/box,
produces
> the same result. (Maybe this is where Google gets its technology?)
Anyway,
> "to die" is still translated as "matrix" for some bizarre reason, and
"say"
> as "word" -- Grumble. I may have to start a fund raising drive just for
> this. I am pretty sure the email I was answering was English out of one of
> these services... meaning my answer probably looks a lot like that to her.
> Unless the translation to Spanish is a lot better than the translation to
> French.
>
> Dana
>
>
> On Fri, 30 May 2003 20:16:12 -0600, Dana Tierney <[EMAIL PROTECTED]>
> wrote:
>
> > I believe this has come up several times on cf-talk, and the consensus
is
> > always a that a human translator is best. While I do agree with this I
do
> > not have a budget for translation at the moment, nor do I have any truly
> > bilingual volunteers. Given enough time I can probably handle French
> > myself but most of our email seems to come from Latin America. The
> > current plan is to set up a link to Google's language tools, but I am
> > really not happy with it. AltaVista's tools seem no better. Does anyone
> > on this list know of a better tool out there?
> >
> > Dana
> >
> > PS - to demonstrate the scope of the problem, I am pasting below the
text
> > of an actual email, translated on Google.
> >
> > First of all, I am very sorry about your baby.  Sometimes these children
> > > matrix despite everything what can be made for them, and we do not
know
> > why.  > > the cause of the syndrome of prune belly is currently not very
> > clear.  The majority of word of doctors > it are not genetic.  We
however
> > know the families which had more one > child of prune belly.  However
the
> > severity of the disease considerably also changes;  > thus a second
force
> > of child of prune belly spout out completely.  There are others familes
>
> > which thus have only one child with the prune belly it can be another
> > factor.  > > I myself AM not a medical professional;  I am a person of
> > sequence which had a friend > with this disease.  I ccing a couple of
the
> > professionals who can be able in measurement > amplify on my answers.  I
> > would strongly suggest looking at all on > the Web site of
> > www.prunebelly.org, including the articles of newspaper, approximately >
> > us page and the forum of support, with which is very actively read by
> > patients
> >> prune belly and parents of the children with the prune belly which made
> > and not > to survive.  I believe that it is the best collection of
> > information on the belly > the prune syndrome outside there.  > > your
> > English seems very good but if the language is an exit I will test >
> > lucky find a Spanish speaker to help you.  We want to translate the
> > website > into other languages, but we are all mostly the volunteers as
> > this proceeds rather > slowly.  > > to answer your questions
specifically
> > -- I do not think that there are genetics > or any other test which can
> > be carried out before you became pregnant.  The belly > the syndrome of
> > prune can be diagnosed in the uterus -- and treated --. the treatment
not
> > > success of guarantee but a diagnosis of syndrome of prune belly is not
> > a death > a sentence.  Look at www.prunebelly.org/AboutUs.html.  To put
> > abruptly, if > you have another child with the syndrome of prune belly
it
> > can only have very soft > symptoms or he can also die, and we do not
know
> > up to now what causes it or > why some kids are so much sicker than
> > others.  If the lives of child it is > probably to need surgery,
probably
> > several consulting-rooms, but if it saw to be > approximately two it
will
> > probably have a happy and reasonably healthy life.  It > seems extremely
> > not very probable that something which this baby with > matrix caused
> > you.  > > hope of I which I answered your questions.  Smell you please
> > free to write behind > so more occur with you.
> >
> > The original text:
> >
> > First of all, I am very sorry about your baby. Sometimes these children
> > do
> >> die in spite of all that can be done for them, and we do not know why.
> >>
> >> The cause of prune belly syndrome is unclear at this time. Most doctors
> > say
> >> it is not genetic. We do however know families who have had more than
> >> one
> >> prune belly child. However the severity of the illness varies widely
> >> also;
> >> so a second prune belly child might do quite well. There are other
> >> familes
> >> who have only one child with prune belly so it may be some other
factor.
> >>
> >> I myself am not a medical professional; I am a web person who had a
> >> friend
> >> with this illness. I am ccing a couple of professionals who may be able
> >> to
> >> amplify on my answers. I would strongly suggest looking at everything
on
> >> the www.prunebelly.org web site, including the journal articles, the
> >> About
> >> Us page and the support forum, which is very actively read by patients
> > with
> >> prune belly and parents of children with prune belly who did and did
not
> >> survive. I believe it is the best collection of information on prune
> >> belly
> >> syndrome out there.
> >>
> >> Your English seems very good but if language is an issue I will attempt
> >> to
> >> find a Spanish speaker to help you. We do want to translate the website
> >> into other languages, but we are mostly all volunteers so this proceeds
> >> rather
> >> slowly.
> >>
> >> To answer your questions specifically -- I do not think there is a
> >> genetic
> >> or other test that can be done before you become pregnant. Prune belly
> >> syndrome can be diagnosed -- and treated -- in utero. Treatment does
not
> >> guarantee success but a diagnosis of prune belly syndrome is not a
death
> >> sentence. Look at www.prunebelly.org/AboutUs.html. To put it bluntly,
if
> >> you have another child with prune belly syndrome it may have only very
> > mild
> >> symptoms or it may also die, and we do not as yet know what causes it
or
> >> why some kids are so much sicker than others. If the child lives it is
> >> likely to need surgery, possibly several surgeries, but if it lives to
> >> be
> >> about two it will probably have a happy and reasonably healthy life. It
> >> does seem extremely unlikely that something you did caused this baby to
> >> die.
> >>
> >> I hope that I have answered your questions. Please feel free to write
> >> back
> >> if more occur to you.
> >
> >
> >
> 
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